chemichs data booklet - helloblen.com
Transcript of chemichs data booklet - helloblen.com
1 Some relevant equations
Topic Equation
13 PV = nRT
22 and C4 c = νλ
51 q = mcΔΤ
83pH = - log
10[H
3O+]
orpH = - log
10[H+]
121 E = hv
152 ΔGΘ = ΔΗΘ - ΤΔSΘ
162 k = Αe-E
α
RT
162 In k = -Eα
RT + InA
162 In k1
k2
= Eα
R ( 1T
2- 1
T1
)
171 ΔGΘ = -RT In K
191 ΔGΘ = -nFEΘ
2 Physical constants and unit conversions
Avogadrorsquos constant (L or NA) = 602 x 1023 mol-1
Gas constant (R) = 831 J K-1 mol-1
Molar volume of an ideal gas at STP = 227 x 10-2 m3 mol-1 = 227 dm3 mol-1
1 dm3 = 1 litre = 1 x 10-3 m3 = 1 x 103 cm3
STP conditions = 273 K and 100 kPaSATP conditions = 298 K and 100 kPa
Topic Equation
A5 atom economy = molar mass of desired productmolar mass of all reactants x 100
A8 nλ = 2dsinθ
B7 pH = pKα + log ( [A-]
[HA] )
B7 log10
I0
I = εlc
C1 Energy density = energy released from fuelvolume of fuel consumed
C1 Specific energy = energy released from fuelmass of fuel consumed
C3 N = N0e -λt
C3 and D8 t 12 = ln 2
λ
C6 Ε = Ε0 - ( RTnF ) ln Q
C7Rate
1Rate
2= M
2M
1
D8 Nt = N
0 (05) tk
Speed of light = 300 x 108 ms-1
Specific heat capacity of water = 418 kJ kg-1K-1 = 418 J g-1 K-1
Planckrsquos constant (h) = 663x 10-34 J sFaradayrsquos constant (F) = 965 x 104 C mol-1
Ionic product constant for water (Kw) = 100 x 10-14 mol2 dm-6 at 298 K
1 amu = 166 x 10-27 kg
3 The electromagnetic spectrum
wavelength nm
10-16 10-14 10-12 10-10 10-8 10-6 10-4 10-2 100 102 104 106 108
| | | | | | | | | | | | |
γ rays X- rays UV IR microwaves radio waves
V I B G Y O R
400 700wavelength nm
energy
4 Fundamental particles
Proton Neutron Electron
Mass (kg) 1672622 x 10-27 1674927 x 10-27 9109383 x 10-31
Charge (C) 1602189 x 10-19 0 -1602189 x 10-19
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| Chemistry Data Booklet
NotesThe booklet cannot be used for paper 1 of the examination (SLP1 and HLP1) but the periodic table given in section 6 will be available as part of these examination papers Clean copies of the booklet must be made available to candidates for papers 2 and 3 (SLP2 HLP2 SLP3 and HLP3)
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5 Names of the elements
Element SymbolAtomic number
actinium Ac 89
aluminium Al 13
americium Am 95
antimony Sb 51
argon Ar 18
arsenic As 33
astatine At 85
barium Ba 56
berkelium Bk 97
beryllium Be 4
bismuth Bi 83
bohrium Bh 107
boron B 5
bromine Br 35
cadmium Cd 48
caesium Cs 55
calcium Ca 20
californium Cf 98
carbon C 6
cerium Ce 58
chlorine Cl 17
chromium Cr 24
cobalt Co 27
copernicium Cn 112
copper Cu 29
curium Cm 96
darmstadtium Ds 110
dubnium Db 105
dysprosium Dy 66
einsteinium Es 99
erbium Er 68
europium Eu 63
fermium Fm 100
fluorine F 9
francium Fr 87
gadolinium Gd 64
gallium Ga 31
germanium Ge 32
gold Au 79
hafnium Hf 72
hassium Hs 108
Element SymbolAtomic number
helium He 2
holmium Ho 67
hydrogen H 1
indium In 49
iodine I 53
iridium Ir 77
iron Fe 26
krypton Kr 36
lanthanum La 57
lawrencium Lr 103
lead Pb 82
lithium Li 3
lutetium Lu 71
magnesium Mg 12
manganese Mn 25
meitnerium Mt 109
mendelevium Md 101
mercury Hg 80
molybdenum Mo 42
neodymium Nd 60
neon Ne 10
neptunium Np 93
nickel Ni 28
niobium Nb 41
nitrogen N 7
nobelium No 102
osmium Os 76
oxygen O 8
palladium Pd 46
phosphorus P 15
platinum Pt 78
plutonium Pu 94
polonium Po 84
potassium K 19
praseodym-ium
Pr 59
promethium Pm 61
protactinium Pa 91
radium Ra 88
radon Rn 86
rhenium Re 75
rhodium Rh 45
Element SymbolAtomic number
roentgenium Rg 111
rubidium Rb 37
ruthenium Ru 44
rutherfor-dium
Rf 104
samarium Sm 62
scandium Sc 21
seaborgium Sg 106
selenium Se 34
silicon Si 14
silver Ag 47
sodium Na 11
strontium Sr 38
sulfur S 16
tantalum Ta 73
technetium Tc 43
tellurium Te 52
terbium Tb 65
thallium Tl 81
thorium Th 90
thulium Tm 69
tin Sn 50
titanium Ti 22
tungsten W 74
uranium U 92
vanadium V 23
xenon Xe 54
ytterbium Yb 70
yttrium Y 39
zinc Zn 30
zirconium Zr 40
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6 The periodic table
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
11H
101
Atomic number
Element
Relative atomicmass
2He400
23Li
694
4Be
901
5B
1081
6C
1201
7N
1401
8O
1600
9F
1900
10Ne
2018
311Na
2299
12Mg
2431
13Al
2698
14Si
2809
15P
3097
16S
3207
17Cl
3545
18Ar
3995
419K
3910
20Ca
4008
21Sc
449
22Ti
4787
23V
5094
24Cr
5200
25Mn
5494
26Fe
5585
27Co
5893
28Ni
5869
29Cu
6355
30Zn
6538
31Ga
6972
32Ge
7263
33As
7492
34Se
7896
35Br
7990
36Kr
8390
537Rb
8547
38Sr
8762
39Y
8891
40Zr
9122
41Nb
9291
42Mo
9596
43Tc
(98)
44Ru
10107
45Rh
10291
46Pd
10642
47Ag
10787
48Cd
11241
49In
11482
50Sn
11871
51Sb
12176
52Te
12760
53I
12690
54Xe
13129
655Cs
13291
56Ba
13733
57 daggerLa
13891
72Hf
17849
73Ta
18095
74W
18384
75Re
18621
76Os
19023
77Ir
19222
78Pt
19508
79Au
19697
80Hg
20059
81Tl
20438
82Pb
20720
83Bi
20898
84Po
(209)
85At
(210)
86Rn
(222)
787Fr
(223)
88Ra
(226)
89DaggerAc
(227)
104Rf
(267)
105Db
(268)
106Sg
(269)
107Bh
(270)
108Hs
(269)
109Mt
(278)
110Ds
(281)
111Rg
(281)
112Cn
(285)
113Uut
(286)
114Uuq(289)
115Uup(288)
116Uuh(293)
117Uus
(294)
118Uuo(294)
dagger58Ce
14012
59Pr
14091
60Nd
14424
61Pm
(145)
62Sm
15036
63Eu
15196
64Gd
15725
65Tb
15893
66Dy
16250
67Ho
16493
68Er
16726
69Tm
16893
70Yb
17305
71Lu
17497
Dagger90Th
23204
91Pa
23104
92U
23803
93Np
(237)
94Pu
(244)
95Am
(243)
96Cm
(247)
97Bk
(247)
98Cf
(251)
99Es
(252)
100Fm
(257)
101Md
(258)
102No
(259)
103Lr
(262)
7 Melting points and boiling points of the elements (at 101325 kPa)
-2592H
-2529
Melting point (degC)
Element
Ionic radius(10-12 m)
He-2689
1805Li
1342
1287Be
2468
2077B
4000
3500C
4827
-2100N
-1958
-2188O
-1830
-2197F
-1881
-2486Ne
-2460
9779Na
8829
6500Mg
1090
6603Al
2519
1414Si
3265
4415P
2805
1152S
4446
-1015Cl
-3404
-1893Ar
-1858
6338K
7588
8420Ca
1484
1541Sc
2836
1670Ti
3287
1910V
3407
1907Cr
2671
1246Mn
2061
1538Fe
2861
1495Co
2927
1455Ni
2913
1085Cu
2560
4195Zn
9070
2977Ga
2229
9382Ge
2833
8168As
6130
2208Se
6848
-7050Br
5878
-1574Kr
-1534
3930Rb
6878
7688Sr
1377
1522Y
3345
1854Zr
4406
2477Nb
4741
2622Mo
4639
2157Tc
4262
2333Ru
4147
1963Rh
3695
1555Pd
2963
9618Ag
2162
3211Cd
7668
1566In
2027
2319Sn
2586
6306Sb
1587
4495Te
9878
1137I
1844
-1118Xe
-1081
2844Cs
6708
7250Ba
1845
9200La
3464
2233Hf
4600
3017Ta
5455
3414W
5555
3453Re
5900
3033Os
5008
2446Ir
4428
1768Pt
3825
1064Au
2836
-3883Hg
3566
3038Tl
1473
3275Pb
1749
2714Bi
1564
2538Po
9620
3018At
3368
-7115Rn
-6185
2700Fr
6768
6998Ra
1140
1050Ac
3200
8 First ionization energy electron affinity and electronegativity of the elements
131 -73
H22
First ionization Electron affinity (kJ mol-1)energy (kJ mol-1) (2nd EA kJ mol-1)
Element
Electronegativity
2372
He
520 -60
Li10
900
Be16
801 -27
B20
1086 -122
C26
1402
N30
1314 -141 (+753)
O34
1681 -328
F40
2081
Ne
496 -53
Na09
738
Mg13
578 -42
Al16
787 -134
Si19
1012 -72
P22
1000 -200 (+545)
S26
1251 -349
Cl32
1520
Ar
419 -48
K08
590 -2
Ca10
633 -18
Sc14
659 -8
Ti15
651 -51
V16
653 -64
Cr17
717
Mn16
762 -15
Fe18
760 -64
Co19
737 -112
Ni19
745 -119
Cu19
906
Zn16
579 -41
Ga18
762 -119
Ge20
944 -78
As22
941 -195
Se26
1140 -325
Br30
1351
Kr
403 -47
Rb08
549 -5
Sr10
600 -30
Y12
640 -41
Zr13
652 -88
Nb16
684 -72
Mo22
702 -53
Tc21
710 -101
Ru22
720 -110
Rh23
804 -54
Pd22
731 -126
Ag19
868
Cd17
558 -29
In18
709 -107
Sn20
831 -101
Sb20
869 -190
Te21
1008 -295
I27
1170
Xe26
376 -46
Cs08
503 -14
Ba09
538 -45
La11
659 -1
Hf13
728 -31
Ta15
759 -79
W17
756 -14
Re19
814 -106
Os22
865 -151
Ir22
864 -205
Pt22
890 -223
Au24
1007
Hg19
589 -36
Tl18
716 -35
Pb18
703 -91
Bi19
812 -183
Po20
-270
At22
1037
Rn
393 -47
Fr07
509 -10
Ra09
499 -34
Ac11
9 Atomic and ionic radii of the elements
32H
Atomic radius(10-12 m)
Element
Ionic radius(10-12 m)
37He
130Li
76 (1+)
99Be
45 (2+)
84B
27 (3+)
75C
16 (4+)
71N
146 (3-)
64O
140 (2-)
60F
133 (1-)
62Ne
160Na
102 (1+)
140Mg
72 (2+)
124Al
54 (3+)
114Si
40 (4+)
109P
38 (5+)
104S
184 (2-)
100Cl
181 (1-)
101Ar
200K
138 (1+)
174Ca
100 (2+)
159Sc
75 (3+)
148Ti
86 (2+)61 (4+)
144V
79 (2+)54 (5+)
130Cr
62 (3+)44 (6+)
129Mn
83 (2+)53 (4+)
124Fe
61 (2+)55 (3+)
118Co
65(+2)55 (+3)
117Ni
69 (2+)
122Cu
77 (1+)73 (2+)
120Zn
74 (2+)
123Ga
62(3+)
120Ge
53 (4+)272(4-)
120As
58 (3+)46 (5+)
118Se
198 (2-)
117Br
196 (1-)
116Kr
215Rb
152 (1+)
190Sr
118 (2+)
176Y
90 (3+)
164Zr
72 (4+)
156Nb
72 (3+)64 (5+)
146Mo
65 (4+)
138Tc
65(4+)
136Ru
68(3+)62 (4+)
134Rh
67 (+3)60 (+4)
130Pd
86(2+) 62(4+)
136Ag
115 (1+)
140Cd
95 (2+)
142In
80(3+)
140Sn
118(2+)69 (4+)
140Sb
76 (3+)
137Te
221 (2-)
136I
220(1-)
136Xe
238Cs
167 (1+)
206Ba
135 (2+)
194La
103 (3+)
164Hf
71 (4+)
158Ta
64(5+)
150W
66 (4+)60(6+)
141Re
63(4+)53(7+)
136Os
63 (4+)55(6+)
132Ir
68(+3)63 (+4)
130Pt
80(2+) 63(4+)
130Au
137 (1+)85 (3+)
132Hg
119 (1+)102 (2+)
144Tl
150 (1+)89 (3)
145Pb
119 (2+)78 (4+)
150Bi
103 (3+) 76(5+)
142Po
97(4+)
148At
146Rn
242Fr
211Ra
201Ac
CHEMISTRY DATA BOOKLET
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CHEMISTRY DATA BOOKLET
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10 Covalent bond lengths
Single bonds (10-12m = pm )
Br C Cl F H I N O P S Si
Br 228 194 214 176 141 247 214 220 227 216
C 194 154 177 138 108 214 147 143 184 182 185
Cl 214 177 199 163 128 232 197 170 203 199 202
F 176 138 163 142 92 257 136 142 154 158 156
H 141 108 128 92 74 160 101 97 142 134 148
I 247 214 232 257 160 267 247 243
N 214 147 197 136 101 146 136 175 174
O 143 170 142 97 136 148 154 161 163
P 220 184 203 154 142 247 154 221 210
S 227 182 199 158 134 175 161 210 205 215
Si 216 185 202 156 148 243 174 163 215 232
Multiple bonds ( 10-12m = pm )
C=C 134 CequivN 116 NequivN 110
CequivC 120 C=O 122 N=O 114
C=C (in benzene) 140 C=S 156 O=O 121
C=N 130 N=N 125 S=S 189
11 Bond enthalpies and average bond enthalpies at 298 K
Single bonds (kJ mol-1 )
Br C Cl F H I N O P S Si
Br 193 285 219 249 366 178 201 264 218 330
C 285 346 324 492 414 228 286 358 264 289 307
Cl 219 324 242 255 431 211 192 206 322 271 400
F 249 492 255 159 567 280 278 191 490 327 597
H 366 414 431 567 436 298 391 463 322 364 323
I 178 228 211 280 298 151 201 184 234
N 286 192 278 391 158 214
O 201 358 206 191 463 201 214 144 363 466
P 264 264 322 490 322 184 363 198
S 218 289 271 327 364 266 293
Si 330 307 400 597 323 234 466 293 226
Multiple bonds ( kJ mol-1 )
C=C 614 CN 890 NN 945
CC 839 C=O 804 N=O 587
C=C (in benzene) 507 C=S 536 O=O 498
C=N 615 N=N 470 S=S 429
CHEMISTRY DATA BOOKLET
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12 Selected compoundsmdashthermodynamic data
Substance Formula State ΔHΘf(kJ mol-1) ΔGΘ
f(kJ mol-1) SΘ (JK-1 mol-1)
methane CH4
g -740 -500 +186
ethane C2H
6g -840 -320 +230
propane C3H
8g -105 -240 +270
butane C4H
10g -126 -170 +310
pentane C5H
12l -173
hexane C6H
14l -199
ethene C2H
4g +520 +680 +220
propene C3H
6g +200 +620 +267
but-1-ene C4H
8g +010 +710 +306
cis-but-2-ene C4H
8g -70 +660 +301
trans-but-2-ene C4H
8g -110 +630 +297
ethyne C2H
2g +228 +211 +201
propyne C3H
4g +185 +194 +248
buta-13-diene C4H
6g +110 +151 +279
cyclohexane C6H
12l -156
benzene C6H
6l +490 +125 +173
methylbenzene C6H
5CH
3l +120
ethylbenzene C6H
5CH
2CH
3l -120
phenylethene C6H
5CHCH
2l +104
chloromethane CH3Cl g -820 -580 +235
dichloromethane CH2Cl
2l -124 +178
trichloromethane CHCl3
l -134 -740 +202
bromomethane CH3Br g -360 -260 +246
iodomethane CH3I l -140 +163
chloroethane C2H
5Cl g -137 -530
bromoethane C2H
5Br l -900 -260 +199
chlorobenzene C6H
5Cl l +110
methanol CH3OH l -239 -167 +127
ethanol C2H
5OH l -278 -175 +161
phenol C6H
5OH s -165 +144
methanal HCHO g -109 -102 +219
ethanal CH3CHO g -166 -133 +264
propanone (CH3)
2CO l -248 +200
methanoic acid HCOOH l -425 -361 +129
ethanoic acid CH3COOH l -484 -390 +160
benzoic acid C6H
5COOH s -385 +168
methylamine CH3NH
2g -23 +320 +243
water H2O l -2858 -2371 +700
steam H2O g -2418 -2286 +1888
carbon monoxide CO g -1105 -1372 +1977
carbon dioxide CO2
g -3935 -3944 +2138
hydrogen bromide HBr g -363 -534 +1987
hydrogen chloride HCl g -923 -953 +1869
hydrogen fluoride HF g -2733 -2754 +1738
hydrogen iodide HI g +265 +17 +2066
CHEMISTRY DATA BOOKLET
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13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
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14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
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19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 2
5 Names of the elements
Element SymbolAtomic number
actinium Ac 89
aluminium Al 13
americium Am 95
antimony Sb 51
argon Ar 18
arsenic As 33
astatine At 85
barium Ba 56
berkelium Bk 97
beryllium Be 4
bismuth Bi 83
bohrium Bh 107
boron B 5
bromine Br 35
cadmium Cd 48
caesium Cs 55
calcium Ca 20
californium Cf 98
carbon C 6
cerium Ce 58
chlorine Cl 17
chromium Cr 24
cobalt Co 27
copernicium Cn 112
copper Cu 29
curium Cm 96
darmstadtium Ds 110
dubnium Db 105
dysprosium Dy 66
einsteinium Es 99
erbium Er 68
europium Eu 63
fermium Fm 100
fluorine F 9
francium Fr 87
gadolinium Gd 64
gallium Ga 31
germanium Ge 32
gold Au 79
hafnium Hf 72
hassium Hs 108
Element SymbolAtomic number
helium He 2
holmium Ho 67
hydrogen H 1
indium In 49
iodine I 53
iridium Ir 77
iron Fe 26
krypton Kr 36
lanthanum La 57
lawrencium Lr 103
lead Pb 82
lithium Li 3
lutetium Lu 71
magnesium Mg 12
manganese Mn 25
meitnerium Mt 109
mendelevium Md 101
mercury Hg 80
molybdenum Mo 42
neodymium Nd 60
neon Ne 10
neptunium Np 93
nickel Ni 28
niobium Nb 41
nitrogen N 7
nobelium No 102
osmium Os 76
oxygen O 8
palladium Pd 46
phosphorus P 15
platinum Pt 78
plutonium Pu 94
polonium Po 84
potassium K 19
praseodym-ium
Pr 59
promethium Pm 61
protactinium Pa 91
radium Ra 88
radon Rn 86
rhenium Re 75
rhodium Rh 45
Element SymbolAtomic number
roentgenium Rg 111
rubidium Rb 37
ruthenium Ru 44
rutherfor-dium
Rf 104
samarium Sm 62
scandium Sc 21
seaborgium Sg 106
selenium Se 34
silicon Si 14
silver Ag 47
sodium Na 11
strontium Sr 38
sulfur S 16
tantalum Ta 73
technetium Tc 43
tellurium Te 52
terbium Tb 65
thallium Tl 81
thorium Th 90
thulium Tm 69
tin Sn 50
titanium Ti 22
tungsten W 74
uranium U 92
vanadium V 23
xenon Xe 54
ytterbium Yb 70
yttrium Y 39
zinc Zn 30
zirconium Zr 40
CHEMISTRY DATA BOOKLET
helloblencom 3
6 The periodic table
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
11H
101
Atomic number
Element
Relative atomicmass
2He400
23Li
694
4Be
901
5B
1081
6C
1201
7N
1401
8O
1600
9F
1900
10Ne
2018
311Na
2299
12Mg
2431
13Al
2698
14Si
2809
15P
3097
16S
3207
17Cl
3545
18Ar
3995
419K
3910
20Ca
4008
21Sc
449
22Ti
4787
23V
5094
24Cr
5200
25Mn
5494
26Fe
5585
27Co
5893
28Ni
5869
29Cu
6355
30Zn
6538
31Ga
6972
32Ge
7263
33As
7492
34Se
7896
35Br
7990
36Kr
8390
537Rb
8547
38Sr
8762
39Y
8891
40Zr
9122
41Nb
9291
42Mo
9596
43Tc
(98)
44Ru
10107
45Rh
10291
46Pd
10642
47Ag
10787
48Cd
11241
49In
11482
50Sn
11871
51Sb
12176
52Te
12760
53I
12690
54Xe
13129
655Cs
13291
56Ba
13733
57 daggerLa
13891
72Hf
17849
73Ta
18095
74W
18384
75Re
18621
76Os
19023
77Ir
19222
78Pt
19508
79Au
19697
80Hg
20059
81Tl
20438
82Pb
20720
83Bi
20898
84Po
(209)
85At
(210)
86Rn
(222)
787Fr
(223)
88Ra
(226)
89DaggerAc
(227)
104Rf
(267)
105Db
(268)
106Sg
(269)
107Bh
(270)
108Hs
(269)
109Mt
(278)
110Ds
(281)
111Rg
(281)
112Cn
(285)
113Uut
(286)
114Uuq(289)
115Uup(288)
116Uuh(293)
117Uus
(294)
118Uuo(294)
dagger58Ce
14012
59Pr
14091
60Nd
14424
61Pm
(145)
62Sm
15036
63Eu
15196
64Gd
15725
65Tb
15893
66Dy
16250
67Ho
16493
68Er
16726
69Tm
16893
70Yb
17305
71Lu
17497
Dagger90Th
23204
91Pa
23104
92U
23803
93Np
(237)
94Pu
(244)
95Am
(243)
96Cm
(247)
97Bk
(247)
98Cf
(251)
99Es
(252)
100Fm
(257)
101Md
(258)
102No
(259)
103Lr
(262)
7 Melting points and boiling points of the elements (at 101325 kPa)
-2592H
-2529
Melting point (degC)
Element
Ionic radius(10-12 m)
He-2689
1805Li
1342
1287Be
2468
2077B
4000
3500C
4827
-2100N
-1958
-2188O
-1830
-2197F
-1881
-2486Ne
-2460
9779Na
8829
6500Mg
1090
6603Al
2519
1414Si
3265
4415P
2805
1152S
4446
-1015Cl
-3404
-1893Ar
-1858
6338K
7588
8420Ca
1484
1541Sc
2836
1670Ti
3287
1910V
3407
1907Cr
2671
1246Mn
2061
1538Fe
2861
1495Co
2927
1455Ni
2913
1085Cu
2560
4195Zn
9070
2977Ga
2229
9382Ge
2833
8168As
6130
2208Se
6848
-7050Br
5878
-1574Kr
-1534
3930Rb
6878
7688Sr
1377
1522Y
3345
1854Zr
4406
2477Nb
4741
2622Mo
4639
2157Tc
4262
2333Ru
4147
1963Rh
3695
1555Pd
2963
9618Ag
2162
3211Cd
7668
1566In
2027
2319Sn
2586
6306Sb
1587
4495Te
9878
1137I
1844
-1118Xe
-1081
2844Cs
6708
7250Ba
1845
9200La
3464
2233Hf
4600
3017Ta
5455
3414W
5555
3453Re
5900
3033Os
5008
2446Ir
4428
1768Pt
3825
1064Au
2836
-3883Hg
3566
3038Tl
1473
3275Pb
1749
2714Bi
1564
2538Po
9620
3018At
3368
-7115Rn
-6185
2700Fr
6768
6998Ra
1140
1050Ac
3200
8 First ionization energy electron affinity and electronegativity of the elements
131 -73
H22
First ionization Electron affinity (kJ mol-1)energy (kJ mol-1) (2nd EA kJ mol-1)
Element
Electronegativity
2372
He
520 -60
Li10
900
Be16
801 -27
B20
1086 -122
C26
1402
N30
1314 -141 (+753)
O34
1681 -328
F40
2081
Ne
496 -53
Na09
738
Mg13
578 -42
Al16
787 -134
Si19
1012 -72
P22
1000 -200 (+545)
S26
1251 -349
Cl32
1520
Ar
419 -48
K08
590 -2
Ca10
633 -18
Sc14
659 -8
Ti15
651 -51
V16
653 -64
Cr17
717
Mn16
762 -15
Fe18
760 -64
Co19
737 -112
Ni19
745 -119
Cu19
906
Zn16
579 -41
Ga18
762 -119
Ge20
944 -78
As22
941 -195
Se26
1140 -325
Br30
1351
Kr
403 -47
Rb08
549 -5
Sr10
600 -30
Y12
640 -41
Zr13
652 -88
Nb16
684 -72
Mo22
702 -53
Tc21
710 -101
Ru22
720 -110
Rh23
804 -54
Pd22
731 -126
Ag19
868
Cd17
558 -29
In18
709 -107
Sn20
831 -101
Sb20
869 -190
Te21
1008 -295
I27
1170
Xe26
376 -46
Cs08
503 -14
Ba09
538 -45
La11
659 -1
Hf13
728 -31
Ta15
759 -79
W17
756 -14
Re19
814 -106
Os22
865 -151
Ir22
864 -205
Pt22
890 -223
Au24
1007
Hg19
589 -36
Tl18
716 -35
Pb18
703 -91
Bi19
812 -183
Po20
-270
At22
1037
Rn
393 -47
Fr07
509 -10
Ra09
499 -34
Ac11
9 Atomic and ionic radii of the elements
32H
Atomic radius(10-12 m)
Element
Ionic radius(10-12 m)
37He
130Li
76 (1+)
99Be
45 (2+)
84B
27 (3+)
75C
16 (4+)
71N
146 (3-)
64O
140 (2-)
60F
133 (1-)
62Ne
160Na
102 (1+)
140Mg
72 (2+)
124Al
54 (3+)
114Si
40 (4+)
109P
38 (5+)
104S
184 (2-)
100Cl
181 (1-)
101Ar
200K
138 (1+)
174Ca
100 (2+)
159Sc
75 (3+)
148Ti
86 (2+)61 (4+)
144V
79 (2+)54 (5+)
130Cr
62 (3+)44 (6+)
129Mn
83 (2+)53 (4+)
124Fe
61 (2+)55 (3+)
118Co
65(+2)55 (+3)
117Ni
69 (2+)
122Cu
77 (1+)73 (2+)
120Zn
74 (2+)
123Ga
62(3+)
120Ge
53 (4+)272(4-)
120As
58 (3+)46 (5+)
118Se
198 (2-)
117Br
196 (1-)
116Kr
215Rb
152 (1+)
190Sr
118 (2+)
176Y
90 (3+)
164Zr
72 (4+)
156Nb
72 (3+)64 (5+)
146Mo
65 (4+)
138Tc
65(4+)
136Ru
68(3+)62 (4+)
134Rh
67 (+3)60 (+4)
130Pd
86(2+) 62(4+)
136Ag
115 (1+)
140Cd
95 (2+)
142In
80(3+)
140Sn
118(2+)69 (4+)
140Sb
76 (3+)
137Te
221 (2-)
136I
220(1-)
136Xe
238Cs
167 (1+)
206Ba
135 (2+)
194La
103 (3+)
164Hf
71 (4+)
158Ta
64(5+)
150W
66 (4+)60(6+)
141Re
63(4+)53(7+)
136Os
63 (4+)55(6+)
132Ir
68(+3)63 (+4)
130Pt
80(2+) 63(4+)
130Au
137 (1+)85 (3+)
132Hg
119 (1+)102 (2+)
144Tl
150 (1+)89 (3)
145Pb
119 (2+)78 (4+)
150Bi
103 (3+) 76(5+)
142Po
97(4+)
148At
146Rn
242Fr
211Ra
201Ac
CHEMISTRY DATA BOOKLET
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CHEMISTRY DATA BOOKLET
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10 Covalent bond lengths
Single bonds (10-12m = pm )
Br C Cl F H I N O P S Si
Br 228 194 214 176 141 247 214 220 227 216
C 194 154 177 138 108 214 147 143 184 182 185
Cl 214 177 199 163 128 232 197 170 203 199 202
F 176 138 163 142 92 257 136 142 154 158 156
H 141 108 128 92 74 160 101 97 142 134 148
I 247 214 232 257 160 267 247 243
N 214 147 197 136 101 146 136 175 174
O 143 170 142 97 136 148 154 161 163
P 220 184 203 154 142 247 154 221 210
S 227 182 199 158 134 175 161 210 205 215
Si 216 185 202 156 148 243 174 163 215 232
Multiple bonds ( 10-12m = pm )
C=C 134 CequivN 116 NequivN 110
CequivC 120 C=O 122 N=O 114
C=C (in benzene) 140 C=S 156 O=O 121
C=N 130 N=N 125 S=S 189
11 Bond enthalpies and average bond enthalpies at 298 K
Single bonds (kJ mol-1 )
Br C Cl F H I N O P S Si
Br 193 285 219 249 366 178 201 264 218 330
C 285 346 324 492 414 228 286 358 264 289 307
Cl 219 324 242 255 431 211 192 206 322 271 400
F 249 492 255 159 567 280 278 191 490 327 597
H 366 414 431 567 436 298 391 463 322 364 323
I 178 228 211 280 298 151 201 184 234
N 286 192 278 391 158 214
O 201 358 206 191 463 201 214 144 363 466
P 264 264 322 490 322 184 363 198
S 218 289 271 327 364 266 293
Si 330 307 400 597 323 234 466 293 226
Multiple bonds ( kJ mol-1 )
C=C 614 CN 890 NN 945
CC 839 C=O 804 N=O 587
C=C (in benzene) 507 C=S 536 O=O 498
C=N 615 N=N 470 S=S 429
CHEMISTRY DATA BOOKLET
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12 Selected compoundsmdashthermodynamic data
Substance Formula State ΔHΘf(kJ mol-1) ΔGΘ
f(kJ mol-1) SΘ (JK-1 mol-1)
methane CH4
g -740 -500 +186
ethane C2H
6g -840 -320 +230
propane C3H
8g -105 -240 +270
butane C4H
10g -126 -170 +310
pentane C5H
12l -173
hexane C6H
14l -199
ethene C2H
4g +520 +680 +220
propene C3H
6g +200 +620 +267
but-1-ene C4H
8g +010 +710 +306
cis-but-2-ene C4H
8g -70 +660 +301
trans-but-2-ene C4H
8g -110 +630 +297
ethyne C2H
2g +228 +211 +201
propyne C3H
4g +185 +194 +248
buta-13-diene C4H
6g +110 +151 +279
cyclohexane C6H
12l -156
benzene C6H
6l +490 +125 +173
methylbenzene C6H
5CH
3l +120
ethylbenzene C6H
5CH
2CH
3l -120
phenylethene C6H
5CHCH
2l +104
chloromethane CH3Cl g -820 -580 +235
dichloromethane CH2Cl
2l -124 +178
trichloromethane CHCl3
l -134 -740 +202
bromomethane CH3Br g -360 -260 +246
iodomethane CH3I l -140 +163
chloroethane C2H
5Cl g -137 -530
bromoethane C2H
5Br l -900 -260 +199
chlorobenzene C6H
5Cl l +110
methanol CH3OH l -239 -167 +127
ethanol C2H
5OH l -278 -175 +161
phenol C6H
5OH s -165 +144
methanal HCHO g -109 -102 +219
ethanal CH3CHO g -166 -133 +264
propanone (CH3)
2CO l -248 +200
methanoic acid HCOOH l -425 -361 +129
ethanoic acid CH3COOH l -484 -390 +160
benzoic acid C6H
5COOH s -385 +168
methylamine CH3NH
2g -23 +320 +243
water H2O l -2858 -2371 +700
steam H2O g -2418 -2286 +1888
carbon monoxide CO g -1105 -1372 +1977
carbon dioxide CO2
g -3935 -3944 +2138
hydrogen bromide HBr g -363 -534 +1987
hydrogen chloride HCl g -923 -953 +1869
hydrogen fluoride HF g -2733 -2754 +1738
hydrogen iodide HI g +265 +17 +2066
CHEMISTRY DATA BOOKLET
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13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
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14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
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19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
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21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
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25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
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31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
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CHEMISTRY DATA BOOKLET
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34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 3
6 The periodic table
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
11H
101
Atomic number
Element
Relative atomicmass
2He400
23Li
694
4Be
901
5B
1081
6C
1201
7N
1401
8O
1600
9F
1900
10Ne
2018
311Na
2299
12Mg
2431
13Al
2698
14Si
2809
15P
3097
16S
3207
17Cl
3545
18Ar
3995
419K
3910
20Ca
4008
21Sc
449
22Ti
4787
23V
5094
24Cr
5200
25Mn
5494
26Fe
5585
27Co
5893
28Ni
5869
29Cu
6355
30Zn
6538
31Ga
6972
32Ge
7263
33As
7492
34Se
7896
35Br
7990
36Kr
8390
537Rb
8547
38Sr
8762
39Y
8891
40Zr
9122
41Nb
9291
42Mo
9596
43Tc
(98)
44Ru
10107
45Rh
10291
46Pd
10642
47Ag
10787
48Cd
11241
49In
11482
50Sn
11871
51Sb
12176
52Te
12760
53I
12690
54Xe
13129
655Cs
13291
56Ba
13733
57 daggerLa
13891
72Hf
17849
73Ta
18095
74W
18384
75Re
18621
76Os
19023
77Ir
19222
78Pt
19508
79Au
19697
80Hg
20059
81Tl
20438
82Pb
20720
83Bi
20898
84Po
(209)
85At
(210)
86Rn
(222)
787Fr
(223)
88Ra
(226)
89DaggerAc
(227)
104Rf
(267)
105Db
(268)
106Sg
(269)
107Bh
(270)
108Hs
(269)
109Mt
(278)
110Ds
(281)
111Rg
(281)
112Cn
(285)
113Uut
(286)
114Uuq(289)
115Uup(288)
116Uuh(293)
117Uus
(294)
118Uuo(294)
dagger58Ce
14012
59Pr
14091
60Nd
14424
61Pm
(145)
62Sm
15036
63Eu
15196
64Gd
15725
65Tb
15893
66Dy
16250
67Ho
16493
68Er
16726
69Tm
16893
70Yb
17305
71Lu
17497
Dagger90Th
23204
91Pa
23104
92U
23803
93Np
(237)
94Pu
(244)
95Am
(243)
96Cm
(247)
97Bk
(247)
98Cf
(251)
99Es
(252)
100Fm
(257)
101Md
(258)
102No
(259)
103Lr
(262)
7 Melting points and boiling points of the elements (at 101325 kPa)
-2592H
-2529
Melting point (degC)
Element
Ionic radius(10-12 m)
He-2689
1805Li
1342
1287Be
2468
2077B
4000
3500C
4827
-2100N
-1958
-2188O
-1830
-2197F
-1881
-2486Ne
-2460
9779Na
8829
6500Mg
1090
6603Al
2519
1414Si
3265
4415P
2805
1152S
4446
-1015Cl
-3404
-1893Ar
-1858
6338K
7588
8420Ca
1484
1541Sc
2836
1670Ti
3287
1910V
3407
1907Cr
2671
1246Mn
2061
1538Fe
2861
1495Co
2927
1455Ni
2913
1085Cu
2560
4195Zn
9070
2977Ga
2229
9382Ge
2833
8168As
6130
2208Se
6848
-7050Br
5878
-1574Kr
-1534
3930Rb
6878
7688Sr
1377
1522Y
3345
1854Zr
4406
2477Nb
4741
2622Mo
4639
2157Tc
4262
2333Ru
4147
1963Rh
3695
1555Pd
2963
9618Ag
2162
3211Cd
7668
1566In
2027
2319Sn
2586
6306Sb
1587
4495Te
9878
1137I
1844
-1118Xe
-1081
2844Cs
6708
7250Ba
1845
9200La
3464
2233Hf
4600
3017Ta
5455
3414W
5555
3453Re
5900
3033Os
5008
2446Ir
4428
1768Pt
3825
1064Au
2836
-3883Hg
3566
3038Tl
1473
3275Pb
1749
2714Bi
1564
2538Po
9620
3018At
3368
-7115Rn
-6185
2700Fr
6768
6998Ra
1140
1050Ac
3200
8 First ionization energy electron affinity and electronegativity of the elements
131 -73
H22
First ionization Electron affinity (kJ mol-1)energy (kJ mol-1) (2nd EA kJ mol-1)
Element
Electronegativity
2372
He
520 -60
Li10
900
Be16
801 -27
B20
1086 -122
C26
1402
N30
1314 -141 (+753)
O34
1681 -328
F40
2081
Ne
496 -53
Na09
738
Mg13
578 -42
Al16
787 -134
Si19
1012 -72
P22
1000 -200 (+545)
S26
1251 -349
Cl32
1520
Ar
419 -48
K08
590 -2
Ca10
633 -18
Sc14
659 -8
Ti15
651 -51
V16
653 -64
Cr17
717
Mn16
762 -15
Fe18
760 -64
Co19
737 -112
Ni19
745 -119
Cu19
906
Zn16
579 -41
Ga18
762 -119
Ge20
944 -78
As22
941 -195
Se26
1140 -325
Br30
1351
Kr
403 -47
Rb08
549 -5
Sr10
600 -30
Y12
640 -41
Zr13
652 -88
Nb16
684 -72
Mo22
702 -53
Tc21
710 -101
Ru22
720 -110
Rh23
804 -54
Pd22
731 -126
Ag19
868
Cd17
558 -29
In18
709 -107
Sn20
831 -101
Sb20
869 -190
Te21
1008 -295
I27
1170
Xe26
376 -46
Cs08
503 -14
Ba09
538 -45
La11
659 -1
Hf13
728 -31
Ta15
759 -79
W17
756 -14
Re19
814 -106
Os22
865 -151
Ir22
864 -205
Pt22
890 -223
Au24
1007
Hg19
589 -36
Tl18
716 -35
Pb18
703 -91
Bi19
812 -183
Po20
-270
At22
1037
Rn
393 -47
Fr07
509 -10
Ra09
499 -34
Ac11
9 Atomic and ionic radii of the elements
32H
Atomic radius(10-12 m)
Element
Ionic radius(10-12 m)
37He
130Li
76 (1+)
99Be
45 (2+)
84B
27 (3+)
75C
16 (4+)
71N
146 (3-)
64O
140 (2-)
60F
133 (1-)
62Ne
160Na
102 (1+)
140Mg
72 (2+)
124Al
54 (3+)
114Si
40 (4+)
109P
38 (5+)
104S
184 (2-)
100Cl
181 (1-)
101Ar
200K
138 (1+)
174Ca
100 (2+)
159Sc
75 (3+)
148Ti
86 (2+)61 (4+)
144V
79 (2+)54 (5+)
130Cr
62 (3+)44 (6+)
129Mn
83 (2+)53 (4+)
124Fe
61 (2+)55 (3+)
118Co
65(+2)55 (+3)
117Ni
69 (2+)
122Cu
77 (1+)73 (2+)
120Zn
74 (2+)
123Ga
62(3+)
120Ge
53 (4+)272(4-)
120As
58 (3+)46 (5+)
118Se
198 (2-)
117Br
196 (1-)
116Kr
215Rb
152 (1+)
190Sr
118 (2+)
176Y
90 (3+)
164Zr
72 (4+)
156Nb
72 (3+)64 (5+)
146Mo
65 (4+)
138Tc
65(4+)
136Ru
68(3+)62 (4+)
134Rh
67 (+3)60 (+4)
130Pd
86(2+) 62(4+)
136Ag
115 (1+)
140Cd
95 (2+)
142In
80(3+)
140Sn
118(2+)69 (4+)
140Sb
76 (3+)
137Te
221 (2-)
136I
220(1-)
136Xe
238Cs
167 (1+)
206Ba
135 (2+)
194La
103 (3+)
164Hf
71 (4+)
158Ta
64(5+)
150W
66 (4+)60(6+)
141Re
63(4+)53(7+)
136Os
63 (4+)55(6+)
132Ir
68(+3)63 (+4)
130Pt
80(2+) 63(4+)
130Au
137 (1+)85 (3+)
132Hg
119 (1+)102 (2+)
144Tl
150 (1+)89 (3)
145Pb
119 (2+)78 (4+)
150Bi
103 (3+) 76(5+)
142Po
97(4+)
148At
146Rn
242Fr
211Ra
201Ac
CHEMISTRY DATA BOOKLET
helloblencom 4
CHEMISTRY DATA BOOKLET
helloblencom 5
10 Covalent bond lengths
Single bonds (10-12m = pm )
Br C Cl F H I N O P S Si
Br 228 194 214 176 141 247 214 220 227 216
C 194 154 177 138 108 214 147 143 184 182 185
Cl 214 177 199 163 128 232 197 170 203 199 202
F 176 138 163 142 92 257 136 142 154 158 156
H 141 108 128 92 74 160 101 97 142 134 148
I 247 214 232 257 160 267 247 243
N 214 147 197 136 101 146 136 175 174
O 143 170 142 97 136 148 154 161 163
P 220 184 203 154 142 247 154 221 210
S 227 182 199 158 134 175 161 210 205 215
Si 216 185 202 156 148 243 174 163 215 232
Multiple bonds ( 10-12m = pm )
C=C 134 CequivN 116 NequivN 110
CequivC 120 C=O 122 N=O 114
C=C (in benzene) 140 C=S 156 O=O 121
C=N 130 N=N 125 S=S 189
11 Bond enthalpies and average bond enthalpies at 298 K
Single bonds (kJ mol-1 )
Br C Cl F H I N O P S Si
Br 193 285 219 249 366 178 201 264 218 330
C 285 346 324 492 414 228 286 358 264 289 307
Cl 219 324 242 255 431 211 192 206 322 271 400
F 249 492 255 159 567 280 278 191 490 327 597
H 366 414 431 567 436 298 391 463 322 364 323
I 178 228 211 280 298 151 201 184 234
N 286 192 278 391 158 214
O 201 358 206 191 463 201 214 144 363 466
P 264 264 322 490 322 184 363 198
S 218 289 271 327 364 266 293
Si 330 307 400 597 323 234 466 293 226
Multiple bonds ( kJ mol-1 )
C=C 614 CN 890 NN 945
CC 839 C=O 804 N=O 587
C=C (in benzene) 507 C=S 536 O=O 498
C=N 615 N=N 470 S=S 429
CHEMISTRY DATA BOOKLET
helloblencom 6
12 Selected compoundsmdashthermodynamic data
Substance Formula State ΔHΘf(kJ mol-1) ΔGΘ
f(kJ mol-1) SΘ (JK-1 mol-1)
methane CH4
g -740 -500 +186
ethane C2H
6g -840 -320 +230
propane C3H
8g -105 -240 +270
butane C4H
10g -126 -170 +310
pentane C5H
12l -173
hexane C6H
14l -199
ethene C2H
4g +520 +680 +220
propene C3H
6g +200 +620 +267
but-1-ene C4H
8g +010 +710 +306
cis-but-2-ene C4H
8g -70 +660 +301
trans-but-2-ene C4H
8g -110 +630 +297
ethyne C2H
2g +228 +211 +201
propyne C3H
4g +185 +194 +248
buta-13-diene C4H
6g +110 +151 +279
cyclohexane C6H
12l -156
benzene C6H
6l +490 +125 +173
methylbenzene C6H
5CH
3l +120
ethylbenzene C6H
5CH
2CH
3l -120
phenylethene C6H
5CHCH
2l +104
chloromethane CH3Cl g -820 -580 +235
dichloromethane CH2Cl
2l -124 +178
trichloromethane CHCl3
l -134 -740 +202
bromomethane CH3Br g -360 -260 +246
iodomethane CH3I l -140 +163
chloroethane C2H
5Cl g -137 -530
bromoethane C2H
5Br l -900 -260 +199
chlorobenzene C6H
5Cl l +110
methanol CH3OH l -239 -167 +127
ethanol C2H
5OH l -278 -175 +161
phenol C6H
5OH s -165 +144
methanal HCHO g -109 -102 +219
ethanal CH3CHO g -166 -133 +264
propanone (CH3)
2CO l -248 +200
methanoic acid HCOOH l -425 -361 +129
ethanoic acid CH3COOH l -484 -390 +160
benzoic acid C6H
5COOH s -385 +168
methylamine CH3NH
2g -23 +320 +243
water H2O l -2858 -2371 +700
steam H2O g -2418 -2286 +1888
carbon monoxide CO g -1105 -1372 +1977
carbon dioxide CO2
g -3935 -3944 +2138
hydrogen bromide HBr g -363 -534 +1987
hydrogen chloride HCl g -923 -953 +1869
hydrogen fluoride HF g -2733 -2754 +1738
hydrogen iodide HI g +265 +17 +2066
CHEMISTRY DATA BOOKLET
helloblencom 7
13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
helloblencom 8
14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
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CHEMISTRY DATA BOOKLET
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34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
8 First ionization energy electron affinity and electronegativity of the elements
131 -73
H22
First ionization Electron affinity (kJ mol-1)energy (kJ mol-1) (2nd EA kJ mol-1)
Element
Electronegativity
2372
He
520 -60
Li10
900
Be16
801 -27
B20
1086 -122
C26
1402
N30
1314 -141 (+753)
O34
1681 -328
F40
2081
Ne
496 -53
Na09
738
Mg13
578 -42
Al16
787 -134
Si19
1012 -72
P22
1000 -200 (+545)
S26
1251 -349
Cl32
1520
Ar
419 -48
K08
590 -2
Ca10
633 -18
Sc14
659 -8
Ti15
651 -51
V16
653 -64
Cr17
717
Mn16
762 -15
Fe18
760 -64
Co19
737 -112
Ni19
745 -119
Cu19
906
Zn16
579 -41
Ga18
762 -119
Ge20
944 -78
As22
941 -195
Se26
1140 -325
Br30
1351
Kr
403 -47
Rb08
549 -5
Sr10
600 -30
Y12
640 -41
Zr13
652 -88
Nb16
684 -72
Mo22
702 -53
Tc21
710 -101
Ru22
720 -110
Rh23
804 -54
Pd22
731 -126
Ag19
868
Cd17
558 -29
In18
709 -107
Sn20
831 -101
Sb20
869 -190
Te21
1008 -295
I27
1170
Xe26
376 -46
Cs08
503 -14
Ba09
538 -45
La11
659 -1
Hf13
728 -31
Ta15
759 -79
W17
756 -14
Re19
814 -106
Os22
865 -151
Ir22
864 -205
Pt22
890 -223
Au24
1007
Hg19
589 -36
Tl18
716 -35
Pb18
703 -91
Bi19
812 -183
Po20
-270
At22
1037
Rn
393 -47
Fr07
509 -10
Ra09
499 -34
Ac11
9 Atomic and ionic radii of the elements
32H
Atomic radius(10-12 m)
Element
Ionic radius(10-12 m)
37He
130Li
76 (1+)
99Be
45 (2+)
84B
27 (3+)
75C
16 (4+)
71N
146 (3-)
64O
140 (2-)
60F
133 (1-)
62Ne
160Na
102 (1+)
140Mg
72 (2+)
124Al
54 (3+)
114Si
40 (4+)
109P
38 (5+)
104S
184 (2-)
100Cl
181 (1-)
101Ar
200K
138 (1+)
174Ca
100 (2+)
159Sc
75 (3+)
148Ti
86 (2+)61 (4+)
144V
79 (2+)54 (5+)
130Cr
62 (3+)44 (6+)
129Mn
83 (2+)53 (4+)
124Fe
61 (2+)55 (3+)
118Co
65(+2)55 (+3)
117Ni
69 (2+)
122Cu
77 (1+)73 (2+)
120Zn
74 (2+)
123Ga
62(3+)
120Ge
53 (4+)272(4-)
120As
58 (3+)46 (5+)
118Se
198 (2-)
117Br
196 (1-)
116Kr
215Rb
152 (1+)
190Sr
118 (2+)
176Y
90 (3+)
164Zr
72 (4+)
156Nb
72 (3+)64 (5+)
146Mo
65 (4+)
138Tc
65(4+)
136Ru
68(3+)62 (4+)
134Rh
67 (+3)60 (+4)
130Pd
86(2+) 62(4+)
136Ag
115 (1+)
140Cd
95 (2+)
142In
80(3+)
140Sn
118(2+)69 (4+)
140Sb
76 (3+)
137Te
221 (2-)
136I
220(1-)
136Xe
238Cs
167 (1+)
206Ba
135 (2+)
194La
103 (3+)
164Hf
71 (4+)
158Ta
64(5+)
150W
66 (4+)60(6+)
141Re
63(4+)53(7+)
136Os
63 (4+)55(6+)
132Ir
68(+3)63 (+4)
130Pt
80(2+) 63(4+)
130Au
137 (1+)85 (3+)
132Hg
119 (1+)102 (2+)
144Tl
150 (1+)89 (3)
145Pb
119 (2+)78 (4+)
150Bi
103 (3+) 76(5+)
142Po
97(4+)
148At
146Rn
242Fr
211Ra
201Ac
CHEMISTRY DATA BOOKLET
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CHEMISTRY DATA BOOKLET
helloblencom 5
10 Covalent bond lengths
Single bonds (10-12m = pm )
Br C Cl F H I N O P S Si
Br 228 194 214 176 141 247 214 220 227 216
C 194 154 177 138 108 214 147 143 184 182 185
Cl 214 177 199 163 128 232 197 170 203 199 202
F 176 138 163 142 92 257 136 142 154 158 156
H 141 108 128 92 74 160 101 97 142 134 148
I 247 214 232 257 160 267 247 243
N 214 147 197 136 101 146 136 175 174
O 143 170 142 97 136 148 154 161 163
P 220 184 203 154 142 247 154 221 210
S 227 182 199 158 134 175 161 210 205 215
Si 216 185 202 156 148 243 174 163 215 232
Multiple bonds ( 10-12m = pm )
C=C 134 CequivN 116 NequivN 110
CequivC 120 C=O 122 N=O 114
C=C (in benzene) 140 C=S 156 O=O 121
C=N 130 N=N 125 S=S 189
11 Bond enthalpies and average bond enthalpies at 298 K
Single bonds (kJ mol-1 )
Br C Cl F H I N O P S Si
Br 193 285 219 249 366 178 201 264 218 330
C 285 346 324 492 414 228 286 358 264 289 307
Cl 219 324 242 255 431 211 192 206 322 271 400
F 249 492 255 159 567 280 278 191 490 327 597
H 366 414 431 567 436 298 391 463 322 364 323
I 178 228 211 280 298 151 201 184 234
N 286 192 278 391 158 214
O 201 358 206 191 463 201 214 144 363 466
P 264 264 322 490 322 184 363 198
S 218 289 271 327 364 266 293
Si 330 307 400 597 323 234 466 293 226
Multiple bonds ( kJ mol-1 )
C=C 614 CN 890 NN 945
CC 839 C=O 804 N=O 587
C=C (in benzene) 507 C=S 536 O=O 498
C=N 615 N=N 470 S=S 429
CHEMISTRY DATA BOOKLET
helloblencom 6
12 Selected compoundsmdashthermodynamic data
Substance Formula State ΔHΘf(kJ mol-1) ΔGΘ
f(kJ mol-1) SΘ (JK-1 mol-1)
methane CH4
g -740 -500 +186
ethane C2H
6g -840 -320 +230
propane C3H
8g -105 -240 +270
butane C4H
10g -126 -170 +310
pentane C5H
12l -173
hexane C6H
14l -199
ethene C2H
4g +520 +680 +220
propene C3H
6g +200 +620 +267
but-1-ene C4H
8g +010 +710 +306
cis-but-2-ene C4H
8g -70 +660 +301
trans-but-2-ene C4H
8g -110 +630 +297
ethyne C2H
2g +228 +211 +201
propyne C3H
4g +185 +194 +248
buta-13-diene C4H
6g +110 +151 +279
cyclohexane C6H
12l -156
benzene C6H
6l +490 +125 +173
methylbenzene C6H
5CH
3l +120
ethylbenzene C6H
5CH
2CH
3l -120
phenylethene C6H
5CHCH
2l +104
chloromethane CH3Cl g -820 -580 +235
dichloromethane CH2Cl
2l -124 +178
trichloromethane CHCl3
l -134 -740 +202
bromomethane CH3Br g -360 -260 +246
iodomethane CH3I l -140 +163
chloroethane C2H
5Cl g -137 -530
bromoethane C2H
5Br l -900 -260 +199
chlorobenzene C6H
5Cl l +110
methanol CH3OH l -239 -167 +127
ethanol C2H
5OH l -278 -175 +161
phenol C6H
5OH s -165 +144
methanal HCHO g -109 -102 +219
ethanal CH3CHO g -166 -133 +264
propanone (CH3)
2CO l -248 +200
methanoic acid HCOOH l -425 -361 +129
ethanoic acid CH3COOH l -484 -390 +160
benzoic acid C6H
5COOH s -385 +168
methylamine CH3NH
2g -23 +320 +243
water H2O l -2858 -2371 +700
steam H2O g -2418 -2286 +1888
carbon monoxide CO g -1105 -1372 +1977
carbon dioxide CO2
g -3935 -3944 +2138
hydrogen bromide HBr g -363 -534 +1987
hydrogen chloride HCl g -923 -953 +1869
hydrogen fluoride HF g -2733 -2754 +1738
hydrogen iodide HI g +265 +17 +2066
CHEMISTRY DATA BOOKLET
helloblencom 7
13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
helloblencom 8
14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
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21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
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25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
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31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 5
10 Covalent bond lengths
Single bonds (10-12m = pm )
Br C Cl F H I N O P S Si
Br 228 194 214 176 141 247 214 220 227 216
C 194 154 177 138 108 214 147 143 184 182 185
Cl 214 177 199 163 128 232 197 170 203 199 202
F 176 138 163 142 92 257 136 142 154 158 156
H 141 108 128 92 74 160 101 97 142 134 148
I 247 214 232 257 160 267 247 243
N 214 147 197 136 101 146 136 175 174
O 143 170 142 97 136 148 154 161 163
P 220 184 203 154 142 247 154 221 210
S 227 182 199 158 134 175 161 210 205 215
Si 216 185 202 156 148 243 174 163 215 232
Multiple bonds ( 10-12m = pm )
C=C 134 CequivN 116 NequivN 110
CequivC 120 C=O 122 N=O 114
C=C (in benzene) 140 C=S 156 O=O 121
C=N 130 N=N 125 S=S 189
11 Bond enthalpies and average bond enthalpies at 298 K
Single bonds (kJ mol-1 )
Br C Cl F H I N O P S Si
Br 193 285 219 249 366 178 201 264 218 330
C 285 346 324 492 414 228 286 358 264 289 307
Cl 219 324 242 255 431 211 192 206 322 271 400
F 249 492 255 159 567 280 278 191 490 327 597
H 366 414 431 567 436 298 391 463 322 364 323
I 178 228 211 280 298 151 201 184 234
N 286 192 278 391 158 214
O 201 358 206 191 463 201 214 144 363 466
P 264 264 322 490 322 184 363 198
S 218 289 271 327 364 266 293
Si 330 307 400 597 323 234 466 293 226
Multiple bonds ( kJ mol-1 )
C=C 614 CN 890 NN 945
CC 839 C=O 804 N=O 587
C=C (in benzene) 507 C=S 536 O=O 498
C=N 615 N=N 470 S=S 429
CHEMISTRY DATA BOOKLET
helloblencom 6
12 Selected compoundsmdashthermodynamic data
Substance Formula State ΔHΘf(kJ mol-1) ΔGΘ
f(kJ mol-1) SΘ (JK-1 mol-1)
methane CH4
g -740 -500 +186
ethane C2H
6g -840 -320 +230
propane C3H
8g -105 -240 +270
butane C4H
10g -126 -170 +310
pentane C5H
12l -173
hexane C6H
14l -199
ethene C2H
4g +520 +680 +220
propene C3H
6g +200 +620 +267
but-1-ene C4H
8g +010 +710 +306
cis-but-2-ene C4H
8g -70 +660 +301
trans-but-2-ene C4H
8g -110 +630 +297
ethyne C2H
2g +228 +211 +201
propyne C3H
4g +185 +194 +248
buta-13-diene C4H
6g +110 +151 +279
cyclohexane C6H
12l -156
benzene C6H
6l +490 +125 +173
methylbenzene C6H
5CH
3l +120
ethylbenzene C6H
5CH
2CH
3l -120
phenylethene C6H
5CHCH
2l +104
chloromethane CH3Cl g -820 -580 +235
dichloromethane CH2Cl
2l -124 +178
trichloromethane CHCl3
l -134 -740 +202
bromomethane CH3Br g -360 -260 +246
iodomethane CH3I l -140 +163
chloroethane C2H
5Cl g -137 -530
bromoethane C2H
5Br l -900 -260 +199
chlorobenzene C6H
5Cl l +110
methanol CH3OH l -239 -167 +127
ethanol C2H
5OH l -278 -175 +161
phenol C6H
5OH s -165 +144
methanal HCHO g -109 -102 +219
ethanal CH3CHO g -166 -133 +264
propanone (CH3)
2CO l -248 +200
methanoic acid HCOOH l -425 -361 +129
ethanoic acid CH3COOH l -484 -390 +160
benzoic acid C6H
5COOH s -385 +168
methylamine CH3NH
2g -23 +320 +243
water H2O l -2858 -2371 +700
steam H2O g -2418 -2286 +1888
carbon monoxide CO g -1105 -1372 +1977
carbon dioxide CO2
g -3935 -3944 +2138
hydrogen bromide HBr g -363 -534 +1987
hydrogen chloride HCl g -923 -953 +1869
hydrogen fluoride HF g -2733 -2754 +1738
hydrogen iodide HI g +265 +17 +2066
CHEMISTRY DATA BOOKLET
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13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
helloblencom 8
14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
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21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 6
12 Selected compoundsmdashthermodynamic data
Substance Formula State ΔHΘf(kJ mol-1) ΔGΘ
f(kJ mol-1) SΘ (JK-1 mol-1)
methane CH4
g -740 -500 +186
ethane C2H
6g -840 -320 +230
propane C3H
8g -105 -240 +270
butane C4H
10g -126 -170 +310
pentane C5H
12l -173
hexane C6H
14l -199
ethene C2H
4g +520 +680 +220
propene C3H
6g +200 +620 +267
but-1-ene C4H
8g +010 +710 +306
cis-but-2-ene C4H
8g -70 +660 +301
trans-but-2-ene C4H
8g -110 +630 +297
ethyne C2H
2g +228 +211 +201
propyne C3H
4g +185 +194 +248
buta-13-diene C4H
6g +110 +151 +279
cyclohexane C6H
12l -156
benzene C6H
6l +490 +125 +173
methylbenzene C6H
5CH
3l +120
ethylbenzene C6H
5CH
2CH
3l -120
phenylethene C6H
5CHCH
2l +104
chloromethane CH3Cl g -820 -580 +235
dichloromethane CH2Cl
2l -124 +178
trichloromethane CHCl3
l -134 -740 +202
bromomethane CH3Br g -360 -260 +246
iodomethane CH3I l -140 +163
chloroethane C2H
5Cl g -137 -530
bromoethane C2H
5Br l -900 -260 +199
chlorobenzene C6H
5Cl l +110
methanol CH3OH l -239 -167 +127
ethanol C2H
5OH l -278 -175 +161
phenol C6H
5OH s -165 +144
methanal HCHO g -109 -102 +219
ethanal CH3CHO g -166 -133 +264
propanone (CH3)
2CO l -248 +200
methanoic acid HCOOH l -425 -361 +129
ethanoic acid CH3COOH l -484 -390 +160
benzoic acid C6H
5COOH s -385 +168
methylamine CH3NH
2g -23 +320 +243
water H2O l -2858 -2371 +700
steam H2O g -2418 -2286 +1888
carbon monoxide CO g -1105 -1372 +1977
carbon dioxide CO2
g -3935 -3944 +2138
hydrogen bromide HBr g -363 -534 +1987
hydrogen chloride HCl g -923 -953 +1869
hydrogen fluoride HF g -2733 -2754 +1738
hydrogen iodide HI g +265 +17 +2066
CHEMISTRY DATA BOOKLET
helloblencom 7
13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
helloblencom 8
14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 7
13 Enthalpies of combustionThe values of the molar enthalpy of combustion (ΔHΘ
C) in the following table refer to a temperature of 298 K and a pressure of 100x105 Pa
Substance Formula lState ΔHΘC
( KJ mol-1 )
hydrogen H2
g -286
sulfur S s -297
carbon (graphite) C s -394
carbon monoxide C0 g -283
methane CH4g -891
ethane C2H
6g -1561
propane C3H
8g -2219
butane C4H
10g -2878
pentane C5H
12l -3509
hexane C6H
14l -4163
octane C8H
18l -5470
cyclohexane C6H
12l -3920
ethene C2H
4g -1411
buta-13-diene C4H
6g -2541
ethyne C2H
2g -1301
benzene C6H
6l -3268
methylbenzene C6H
5CH
3l -3910
naphthalene C10
H8
s -5156
chloroethane C2H
5Cl g -1413
iodoethane C2H
5I l -1463
trichloromethane CHCl3
l -473
methanol CH3OH l -726
ethanol C2H
5OH l -1367
propan-1-ol C3H
7OH l -2021
butan-1-ol C4H
9OH l -2676
cyclohexanol C6H
11OH s -3728
phenol C6H
5OH s -3053
ethoxyethane (C2H
5)
2O l -2724
methanal HCHO g -571
ethanal CH3CHO g -1167
benzaldehyde C6H
5CHO l -3525
propanone (CH3)
2CO l -1790
pentan-3-one (C2H
5)
2CO l -3100
phenylethanone CH3COC
6H
5l -4149
methanoic acid HCOOH l -255
ethanoic acid CH3COOH l -874
benzoic acid C6H
5COOH s -3228
ethanedioic acid (COOH)2
s -243
ethyl ethanoate CH3COOC
2H
5l -2238
ethanamide CH3CONH
2s -1186
methylamine CH3NH
2g -1086
phenylamine C6H
5NH
2l -3393
nitrobenzene C6H
5NO
2l -3088
urea CO(NH2)
2s -633
glucose C6H
12O
6s -2803
sucrose C12
H22
O11
s -5640
CHEMISTRY DATA BOOKLET
helloblencom 8
14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 8
14 Common oxidation numbers of the 3d ions
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6
+7
15 Spectrochemical series
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an octahedral complex
I- lt Br- lt S2- lt Cl- lt F- lt OH- lt H2O lt SCN- lt NH
3 lt CN- asymp CO
16 Ligands
Ligands can be arranged in a spectrochemical series according to the energy difference they produce between the two sets of d-orbitals in an o
12 - ethanediamine
ethanedioate EDTA
17 Colour wheel
Red
Violet
Orange
Blue
Yellow
575 nm
700 nm
400 nm
491 nm
585 nm
424 nm
647 nm
Green
18 Lattice enthalpies at 298 K (experimental values)
The lattice enthalpy values (ΔHΘlattice
) given relate to the endothermic process M
aX
b(s)rarraMb+(g)+bXa-(g) in which the gaseous ions of a crys-
tal are separated to an infinite distance from each other
Experimental valuesThe data in these tables are experimental values obtained by means of a suitable BornndashHaber cycle
Alkali metal
halides
ΔHΘlattice ( kJ mol-1 )
F Cl Br I
Li 1049 864 820 764
Na 930 790 754 705
K 829 720 691 650
Rb 795 695 668 632
Cs 759 670 647 613
Other substances ΔHΘlattice ( KJ mol-1 )
CaF2
2651
BeCl2
3033
MgCl2
2540
CaCl2
2271
SrCl2
2170
BaCl2
2069
MgO 3791
CaO 3401
SrO 3223
BaO 3054
CuCl22824
AgF 974
AgCl 918
AgBr 905
AgI 892
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 9
19 Enthalpies of aqueous solutions
SoluteΔHΘsol
( kJ mol-1 )
NH4Cl +1478
NH4NO
3+2569
LiF +473
LiCl -3703
LiBr -4883
LiI -6330
NaF +091
NaCl +388
NaBr -060
NaI -753
KF -1773
KCl +1722
KBr +1987
KI +2033
RbF -2611
RbCl +1728
RbBr +2188
RbI +2510
CsF -3686
CsCl +1778
CsBr +2598
CsI +3335
20 Enthalpies of hydration
CationsΔHΘhyd
(kJ mol-1)Anions
ΔHΘhyd(kJ mol-1)
Li+ -538 F- -504
Na+ -424 Cl- -359
K+ -340 Br- -328
Rb+ -315 I- -287
Cs+ -291 ClO 3- -331
Be2+ -2524 BrO 3- -358
Mg2+ -1963 IO 3- -446
Ca2+ -1616 ClO 4- -205
Sr2+ -1483 OH- -519
Ba2+ -1346 CN- -341
Ra2+ -1335 NO 3- -316
Al3+ -4741 HCO 3- -383
Ga3+ -4745 CO 32 - -1486
In3+ -4171 HSO 4- -362
Tl3+ -4163 SO 42 - -1099
Tl+ -346 PO 43 - -2921
Sn2+ -1587
Pb2+ -1523
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 10
21 Strengths of organic acids and bases
The acid strengths in the following tables are given in terms of pKa
values where pKa= -log
10K
a The dissociation constant K
a values are
for aqueous solutions at 298 K Base strengths are given in terms of
pKb values
Carboxylic acids
Name Formula pKa
methanoic HCOOH 375
ethanoic CH3COOH 476
propanoic CH3CH
2COOH 487
butanoic CH3(CH
2)
2COOH 483
2-methylpropanoic (CH3)
2CHCOOH 484
pentanoic CH3(CH
2)
3COOH 483
22-dimethylpropanoic (CH3)
3CCOOH 503
benzoic C6H
5COOH 420
phenylethanoic C6H
5CH
2COOH 431
Halogenated carboxylic acids
Name Formula pKa
chloroethanoic CH2ClCOOH 287
dichloroethanoic CHCl2COOH 135
trichloroethanoic CCl3COOH 066
fluoroethanoic CH2FCOOH 259
bromoethanoic CH2BrCOOH 290
iodoethanoic CH2ICOOH 318
Phenols
Name Formula pKa
phenol C6H
5OH 999
2-nitrophenol O2NC
6H
4OH 723
3-nitrophenol O2NC
6H
4OH 836
4-nitrophenol O2NC
6H
4OH 715
24-dinitrophenol (O2N)
2C
6H
3OH 407
246-trinitrophenol (O2N)
3C
6H
2OH 042
Alcohols
Name Formula PKa
methanol CH3OH 155
ethanol C2H
5OH 155
Amines
Name Formula PKb
ammonia NH3
475
methylamine CH3NH
2334
ethylamine CH3CH
2NH
2335
dimethylamine (CH3)
2NH 327
trimethylamine (CH3)
3N 420
diethylamine (C2H
5)
2NH 316
triethylamine (C2H
5)
3N 325
phenylamine C6H
5NH
2913
22 Acid-base indicators
Colour change
Indicator pKa
pH range Acid Alkali
methyl orange
37 31ndash44 red yellow
bromophe-nol blue
42 30ndash46 yellow blue
bromocresol green
47 38ndash54 yellow blue
methyl red 51 44ndash62 red yellow
bromothy-mol blue
70 60ndash76 yellow blue
phenol red 79 68ndash84 yellow red
phenol-phthalein
96 83ndash100 colourless pink
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 11
23 Values of the ionization constant of water
Temperature (degC) Kw value
0 0113 x 10-14
5 0185 x 10-14
10 0292 x 10-14
15 0453 x 10-14
20 0684 x 10-14
25 100 x 10-14
30 147 x 10-14
35 209 x 10-14
40 292 x 10-14
45 402 x 10-14
50 543 x 10-14
55 724 x 10-14
60 955 x 10-14
65 124 x 10-14
70 159 x 10-14
75 201 x 10-14
80 252 x 10-14
85 313 x 10-14
90 383 x 10-14
95 466 x 10-14
100 560 x 10-14
24 Standard electrode potentials at 298 K
Oxidized species Reduced species EΘ(V)
Li+(aq)+e- Li(s) -304
K+(aq)+e- K(s) -293
Ca2+(aq)+2e- Ca(s) -287
Na+(aq)+e- Na(s) -271
Mg2+(aq)+2e- Mg(s) -237
Al3+(aq)+3e- Al(s) -166
Mn2+(aq)+2e- Mn(s) -118
H2O(l)+e-
12 H
2(g)+OH-(aq) -083
Zn2+(aq)+2e- Zn(s) -076
Fe2+(aq)+2e- Fe(s) -045
Ni2+(aq)+2e- Ni(s) -026
Sn2+(aq)+2e- Sn(s) -014
Pb2+(aq)+2e- Pb(s) -013
H+(aq)+e-12 H
2(g) 000
Cu2+(aq)+e- Cu+(aq) +015
SO 42 -(aq)+4H+(aq)+2e- H
2SO
3(aq)+H
2O(l) +017
Cu2+(aq)+2e- Cu(s) +034
12 O
2(g)+H
2O(l)+2e- 2OH-(aq) +040
Cu+(aq)+e- Cu(s) +052
12 I
2(s)+e- I-(aq) +054
Fe3+(aq)+e- Fe2+(aq) +077
Ag+(aq)+e- Ag(s) +080
12 Br
2(l)+e- Br-(aq) +109
12 O
2(g)+2H
2(aq)+2e- H2O(l) +123
Cr2O
72 -(aq)+14H+(aq)+6e- 2Cr3+(aq)+7H
2O(l) +136
12 Cl
2(g)+e- Cl-(aq) +136
MnO4-(aq)+8H+(aq)+5e- Mn2++4H
2O(l) +151
12 F
2(g)+e- F-(aq) +287
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 12
25 Activity series
Increasing activity
Li
Cs
Rb
K
Ba
Sr
Ca
Na
Mg
Be
Al
C
Zn
Cr
Fe
Cd
Co
Ni
Sn
Pb
H
Sb
As
Bi
Cu
Ag
Pd
Hg
Pt
Au
26 Infrared dataCharacteristic ranges for infrared absorption due to stretching vibrations in organic molecules
Bond Organic molecules Wavenumber (cm-1) Intensity
CndashI iodoalkanes 490ndash620 strong
CndashBr bromoalkanes 500ndash600 strong
CndashCl chloroalkanes 600ndash800 strong
CndashF fluoroalkanes 1000ndash1400 strong
CndashO alcohols esters ethers 1050ndash1410 strong
C=C alkenes 1620ndash1680 medium-weak multiple bands
C=O aldehydes ketones carboxylic acids and esters 1700ndash1750 strong
CequivC alkynes 2100ndash2260 variable
OndashH hydrogen bonding in carboxylic acids 2500ndash3000 strong very broad
CndashH alkanes alkenes arenes 2850ndash3090 strong
OndashH hydrogen bonding in alcohols and phenols 3200ndash3600 strong broad
NndashH primary amines 3300ndash3500 medium two bands
27 1H NMR data
Typical proton chemical shift values (δ) relative to tetramethylsilane (TMS) =0R represents an alkyl group and Hal represents F Cl Br or IThese values may vary in different solvents and conditions
Type of proton Chemical shift (ppm)
mdashCH3
09ndash10
mdashCH2-R 13ndash14
mdashR2CH 15
20ndash25
CR CH2
O22ndash27
CH3 25ndash35
mdashCequivCmdashH 18ndash31
mdashCH2-Hal 35ndash44
RmdashOmdashCH2mdash 33ndash37
CO
R O CH2
37ndash48
CO
R O H90ndash130
RmdashOmdashH 10ndash60
mdashHC=CH2
45ndash60
OH
40ndash120
H 69ndash90
CHR
O
94ndash100
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
28 Mass spectral fragments lost
Mass lost Fragment lost
15 CH3
17 OH
18 H2O
28 CH2=CH
2 C=O
29 CH3CH
2 CHO
31 CH3O
45 COOH
29 Triangular bonding diagram
Ionic
Polarcovalent
CovalentMetallic
van Arkel-Ketelaar Triangle of Bonding
Electronegativity difference
Electronegativitydifference
Δχ = | χa - x
b |
30
25
20
15
10
05
0
079 10 15 20 25 30 35 40
8 92
25 75
50 50
75 25
100 0
covalent ionic
Average electronegativity Σχ = (χa+χ
b)
2
30 Resin identification codes
Resin Identification Code (RIC) Plastic types
1PETE
polyethyleneterephthalate
2HDPE
high-densitypolyethylene
3PVC
polyvinylchloride
4LDPE
low-densitypolyethylene
5PP
polypropylene
6PS
polystyrene
7OTHER
other
CHEMISTRY DATA BOOKLET
helloblencom 13
31 Representations of some materials molecules
Cln
Clm
O
O
polychlorinated biphenyls 14-dioxin
OCln Clm
polychlorinated dibenzofuran
O
OCl
Cl
Cl
Cl
2378-tetrachlorodibenzodioxin
O
O
ClnClm
polychlorinated dibenzo-p-dioxin
32 Solubility product constants at 298 K
Compound Ksp
BaCO3
258 x 10-9
Ba(OH)2 8H
2O 255 x 10-4
BaSO4
108 x 10-10
CdCO3
10 x 10-12
Cd(OH)2
72 x 10-15
PbCO3
740 x 10-14
Pb(OH)2
143 x 10-20
PbSO4
253 x 10-8
Hg2CO
336 x 10-17
Hg2SO
465 x 10-7
NiCO3
142 x 10-7
Ni(OH)2
548 x 10-16
Ag2CO
3846 x 10-12
Ag2SO
4120 x 10-5
ZnCO3
146 x 10-10
Zn(OH)2
30 x 10-17
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
33 2-amino acids
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
alanine AlaH2N CH
CH3
COOH60
arginine Arg
H2N CHCH2
COOHCH2 CH2 NH C NH2
NH108
asparag-ine
Asn
H2N CHCH2
COOHC NH2
O54
aspartic acid
AspH2N CH
CH2
COOHCOOH 28
cysteine CysH2N CH
CH2
COOHSH
51
glutamic acid
GluH2N CH
CH2
COOHCH2 COOH
32
glu-tamine
Gln
H2N CHCH2
COOHCH2 C
ONH2 57
glycine Gly H2N CH2 COOH 60
histidine His
H2N CH
CH2
NN
COOH
H
76
isoleu-cine
IleH2N CH
CHH3CCOOHCH2 CH3
60
leucine Leu
H2N CHCH2
CHH3C CH3
COOH
60
lysine LysH2N CH
CH2
COOHCH2 CH2 CH2 NH2
97
methio-nine
MetH2N CH
CH2 CH2 S CH3
COOH57
phenyla-lanine
Phe
H2N CH
CH2
COOH
55
Com-mon name
Symbol Structural formula
pH of isoe-
lectric point
proline Pro HNCOOH
63
serine SerH2N CH
CH2
COOHOH 57
threonine ThrH2N CH
CHCOOH
H3C OH56
trypto-phan
Trp
H2N CH
CH2
NH
COOH
59
tyrosine Tyr
H2N CH
CH2
OH
COOH
57
valine ValH2N CH
CHCOOHCH3H3C
60
CHEMISTRY DATA BOOKLET
helloblencom 14
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
CHEMISTRY DATA BOOKLET
helloblencom 15
34 Lipids carbohydrates and nucleotide components
Lipids
Octanoic acid CH3(CH
2)
6COOH
Lauric acid CH3(CH
2)
10COOH
Palmitic acid CH3(CH
2)
14COOH
Stearic acid CH3(CH
2)
16COOH
Oleic acid CH3(CH
2)
7CH=CH(CH
2)
7COOH
Linoleic acid CH3(CH
2)
4(CH=CHCH
2)
2(CH
2)
6COOH
α-Linolenic acid CH3CH
2(CH=CHCH
2)
3(CH
2)
6COOH
HO
HC
H3C CH2
CH3
CH3CH2
CH2CH
CH3
CH3
cholesterol
Carbohydrates
H C OCH OHCHO HCH OHCH OHCH2
O
HO
H
H
H
H
OH
OH
CH2OH
HOH
CH2OHC OCHO HCH OHCH OHCH2OH
straight chain α-glucose straight chain glucose fructose
OH
CH2OH
H
CH2OH
OH H
H OH
O
H
OH
H
CH2OH
OH OH
H H
O
fructose ribose
H
OH
H
CH2OH
OH H
H H
O
deoxyribose
Nitrogenous bases
HCN
CC
CN
NCH
N
H
NH2
CN
CC
CNH
NCH
N
HNH2
O
NH2
CNC
NCHCH
HO
adenine guanine cytosine
CNC
NCHCH
HO
OH
CNC
NCHC
HO
OH
CH3
uracil thymine
35 Vitamins and pigments
Vitamins
CH3
CH3
CH3
HC
CHCCH3
CHCH
CHC
CH
CH3
CH2OH
retinol (vitamin A)
CHCH2
OH
O
O
OH
HO
HO
CH2CH
CHCH3
CH2
HO
CH3
CH2 CH2CH2 CH CH3
CH3
ascorbic acid (vitamin C) vitamin D (D3)
Pigments
NNCH
NNCH
CH2
RCHCH2
H3C
CH3
CH2OCCH2
COO
CH3
Mg2+
C20H39
O OCH3
H
CH3
H
H
NHC
N
CH
NNFe2+
CH3
CH3
CH
CH3
CH2
CH2
OHO
CH3
CH2
CH2
HO O
CHCH2
CH2
chlorophyll heme B
O
ROH
RO
OHO glucose
O+
ROH
ROH
OHO glucose
quinoidal base (blue) flavylium cation (red)
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
α-carotene
CH3
CHCH
CCH3
CHCH
CHCCH3
CHCH
CHCH
CCH3
CHCH
CHCCH3
CHCH
CH3
CH3
CH3
CH3
CH3
β-carotene
CH3
CH3
CH3
CHCH
CCH
CH3
CHCHC
H3C CHCH
O
CHCH3 CH3
CH3
CHC
CH
CH3
CHCH
CCH
CH3
CHO
11-cis-retinal all-trans-retinal
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014
36 Binding energy curve
Ave
rage
bin
ding
ene
rgy
per
nucl
eon
(MeV
)
9
8
7
6
5
4
3
2
1
0
0 30 60 90 120 150 180 210 240 270
Number of nucleons in nucleus
37 Representations of some medicinal molecules
Carbohydrates
aspirin penicillin (general structure) ibuprofen paracetamol (acetaminophen)
morphine codeine diamorphine (heroin)
ON
CH3
CH3
SNH
NHN+
H3CO
Ondash
omeprazole ranitidine
NH
OCH3
CH3
CH3
O CH3
ONH2
O
OH
OH
NH
ONH
O
OH
O
OH
NH2NH
CH3
O NH
OH
O
O
OCH3
O
O
OO CH3
O
OH O
O
CH3CH3
CH3
CH3OH
oseltamivir zanamivir taxol
CHEMISTRY DATA BOOKLET
helloblencom 16Adapted from IB Chemistry Data Booklet published in June 2014