Table 5D.1 Acidity and basicity constants* at 298.15 K Acid/Base pk, K, pk, Strongest weak acids 3.3 x 10-14 Trichloroethanoic acid (trichloroacetic acid), CCI,COOH 13.48 3.0 x 10-1 0.52 Benzenesulfonic acid, C3H§SO3H 5.0 x 10-14 13.30 2 x 10-1 0.70 lodic acid, HIO, 5.9 x 10-14 13.23 1.7 x 10-1 0.77 1.6 x 10-2 1.0 x 10-2 Sulfurous acid, H,SO3 6.3 x 10-13 12.19 1.81 Weakest weak bases Chlorous acid, HCIO2 1.0 x 10-12 12.00 2.00 Urea, CO(NH,), 1.3 x 10-14 13.90 7.7 x 10-1 0.10 Phosphoric acid, H;PO4 1.3 x 10-12 11.88 7.6 x 10-3 2.12 Aniline, C,H;NH2 Pyridine, C,H,N 4.3 x 10-10 9.37 2.3 x 10-5 4.63 Chloroethanoic acid (chloroacetic acid), CH,CICOOH Lactic acid, CH,CH(OH)COOH Nitrous acid, HNO, 7.1 x 10-12 11.15 1.4 x 10-3 2.85 1.8 x 10-9 8.75 5.6 x 10-6 5.35 Hydroxylamine, NH,OH 1.1 x 10-8 7.97 9.1 x 10-7 6.03 1.2 x 10-11 10.92 8.4 x 104 3.08 Nicotine, C10H,N2 1.0 x 106 5.98 1.0 x 10-8 8.02 - 2.3 x 10-11 10.63 4.3 x 104 3.37 Morphine, C1,H19OSN 1.6 x 10-6 5.79 6.3 x 10-9 8.21 Hydrofluoric acid, HF 2.9 x 10-11 10.55 3.5 x 104 3.45 Hydrazine, NH,NH, 1.7 x 10-6 5.77 5.9 x 10-9 8.23 Methanoic acid (formic acid), HCOOH 5.6 x 10-11 10.25 1.8 x 104 3.75 Ammonia, NH3 1.8 x 10-5 4.75 5.6 x 10-10 9.25 Benzoic acid, C,H,COOH 1.5 x 10-10 9.81 6.5x 104 4.19 Trimethylamine, (CH);N 6.5 x 10-5 4.19 1.5 x 10-10 9.81 Ethanoic acid (acetic acid), CH,COOH Carbonic acid, H,CO, 5.6 x 104 4.3 x 10-7 5.6 x 10-10 9.25 4.75 Methylamine, CH;NH2 Dimethylamine, (CH,),NH Ethylamine, C,H;NH, 3.6 x 104 3.44 2.8x 10-1 10.56 2.3x 10-8 7.63 6.37 5.4 x 104 3.27 1.9 x 10-11 10.73 Hypochlorous acid, HCIO Hypobromous acid, HBRO Boric acid, B(OH), 3.3 x 10-7 6.47 3.0 x 10-8 7.53 6.5 x 104 3.19 1.5 x 10-11 10.81 5.0 x 106 5.31 2.0 x 10-9 8.69 Triethylamine, (C,H;);N 1.0 x 10-9 2.99 1.0 x 10-11 11.01 1.4 x 10-5 4.86 7.2 x 10-10 9.14 Strongest weak bases Hydrocyanic acid, HCN Phenol, CgH;OH 2.0x 10-5 4.69 4.9 x 10-10 9.31 7.7 x 10-5 4.11 1.3 x 10-10 9.89 Hypoiodous acid, HIO 4.3 x 104 3.36 2.3 x 10-11 10.64 *Values for polyprotic acids-those capable of donating more than one proton-refer to the first deprotonation. The proton transfer equilibrium is B(OH),(aq) + 2 H,0(1)= H,O*(aq) + B(OH), (aq). Weakest weak acids

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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Using the values for pKa or pKb, as appropriate, fromthe given table, determine the fraction of solute deprotonated or protonated in (a) 0.25 M C6H5COOH(aq), (b) 0.150 M NH2NH2 (aq) (hydrazine), (c) 0.112 M (CH3)3N(aq) (trimethylamine).

Table 5D.1
Acidity and basicity constants* at 298.15 K
Acid/Base
pk,
K,
pk,
Strongest weak acids
3.3 x 10-14
Trichloroethanoic acid (trichloroacetic acid),
CCI,COOH
13.48
3.0 x 10-1
0.52
Benzenesulfonic acid, C3H§SO3H
5.0 x 10-14
13.30
2 x 10-1
0.70
lodic acid, HIO,
5.9 x 10-14
13.23
1.7 x 10-1
0.77
1.6 x 10-2
1.0 x 10-2
Sulfurous acid, H,SO3
6.3 x 10-13
12.19
1.81
Weakest weak bases
Chlorous acid, HCIO2
1.0 x 10-12
12.00
2.00
Urea, CO(NH,),
1.3 x 10-14
13.90
7.7 x 10-1
0.10
Phosphoric acid, H;PO4
1.3 x 10-12
11.88
7.6 x 10-3
2.12
Aniline, C,H;NH2
Pyridine, C,H,N
4.3 x 10-10
9.37
2.3 x 10-5
4.63
Chloroethanoic acid (chloroacetic acid),
CH,CICOOH
Lactic acid, CH,CH(OH)COOH
Nitrous acid, HNO,
7.1 x 10-12
11.15
1.4 x 10-3
2.85
1.8 x 10-9
8.75
5.6 x 10-6
5.35
Hydroxylamine, NH,OH
1.1 x 10-8
7.97
9.1 x 10-7
6.03
1.2 x 10-11
10.92
8.4 x 104
3.08
Nicotine, C10H,N2
1.0 x 106
5.98
1.0 x 10-8
8.02 -
2.3 x 10-11
10.63
4.3 x 104
3.37
Morphine, C1,H19OSN
1.6 x 10-6
5.79
6.3 x 10-9
8.21
Hydrofluoric acid, HF
2.9 x 10-11
10.55
3.5 x 104
3.45
Hydrazine, NH,NH,
1.7 x 10-6
5.77
5.9 x 10-9
8.23
Methanoic acid (formic acid), HCOOH
5.6 x 10-11
10.25
1.8 x 104
3.75
Ammonia, NH3
1.8 x 10-5
4.75
5.6 x 10-10
9.25
Benzoic acid, C,H,COOH
1.5 x 10-10
9.81
6.5x 104
4.19
Trimethylamine, (CH);N
6.5 x 10-5
4.19
1.5 x 10-10
9.81
Ethanoic acid (acetic acid), CH,COOH
Carbonic acid, H,CO,
5.6 x 104
4.3 x 10-7
5.6 x 10-10
9.25
4.75
Methylamine, CH;NH2
Dimethylamine, (CH,),NH
Ethylamine, C,H;NH,
3.6 x 104
3.44
2.8x 10-1
10.56
2.3x 10-8
7.63
6.37
5.4 x 104
3.27
1.9 x 10-11
10.73
Hypochlorous acid, HCIO
Hypobromous acid, HBRO
Boric acid, B(OH),
3.3 x 10-7
6.47
3.0 x 10-8
7.53
6.5 x 104
3.19
1.5 x 10-11
10.81
5.0 x 106
5.31
2.0 x 10-9
8.69
Triethylamine, (C,H;);N
1.0 x 10-9
2.99
1.0 x 10-11
11.01
1.4 x 10-5
4.86
7.2 x 10-10
9.14
Strongest weak bases
Hydrocyanic acid, HCN
Phenol, CgH;OH
2.0x 10-5
4.69
4.9 x 10-10
9.31
7.7 x 10-5
4.11
1.3 x 10-10
9.89
Hypoiodous acid, HIO
4.3 x 104
3.36
2.3 x 10-11
10.64
*Values for polyprotic acids-those capable of donating more than one proton-refer to the first deprotonation.
The proton transfer equilibrium is B(OH),(aq) + 2 H,0(1)= H,O*(aq) + B(OH), (aq).
Weakest weak acids
Transcribed Image Text:Table 5D.1 Acidity and basicity constants* at 298.15 K Acid/Base pk, K, pk, Strongest weak acids 3.3 x 10-14 Trichloroethanoic acid (trichloroacetic acid), CCI,COOH 13.48 3.0 x 10-1 0.52 Benzenesulfonic acid, C3H§SO3H 5.0 x 10-14 13.30 2 x 10-1 0.70 lodic acid, HIO, 5.9 x 10-14 13.23 1.7 x 10-1 0.77 1.6 x 10-2 1.0 x 10-2 Sulfurous acid, H,SO3 6.3 x 10-13 12.19 1.81 Weakest weak bases Chlorous acid, HCIO2 1.0 x 10-12 12.00 2.00 Urea, CO(NH,), 1.3 x 10-14 13.90 7.7 x 10-1 0.10 Phosphoric acid, H;PO4 1.3 x 10-12 11.88 7.6 x 10-3 2.12 Aniline, C,H;NH2 Pyridine, C,H,N 4.3 x 10-10 9.37 2.3 x 10-5 4.63 Chloroethanoic acid (chloroacetic acid), CH,CICOOH Lactic acid, CH,CH(OH)COOH Nitrous acid, HNO, 7.1 x 10-12 11.15 1.4 x 10-3 2.85 1.8 x 10-9 8.75 5.6 x 10-6 5.35 Hydroxylamine, NH,OH 1.1 x 10-8 7.97 9.1 x 10-7 6.03 1.2 x 10-11 10.92 8.4 x 104 3.08 Nicotine, C10H,N2 1.0 x 106 5.98 1.0 x 10-8 8.02 - 2.3 x 10-11 10.63 4.3 x 104 3.37 Morphine, C1,H19OSN 1.6 x 10-6 5.79 6.3 x 10-9 8.21 Hydrofluoric acid, HF 2.9 x 10-11 10.55 3.5 x 104 3.45 Hydrazine, NH,NH, 1.7 x 10-6 5.77 5.9 x 10-9 8.23 Methanoic acid (formic acid), HCOOH 5.6 x 10-11 10.25 1.8 x 104 3.75 Ammonia, NH3 1.8 x 10-5 4.75 5.6 x 10-10 9.25 Benzoic acid, C,H,COOH 1.5 x 10-10 9.81 6.5x 104 4.19 Trimethylamine, (CH);N 6.5 x 10-5 4.19 1.5 x 10-10 9.81 Ethanoic acid (acetic acid), CH,COOH Carbonic acid, H,CO, 5.6 x 104 4.3 x 10-7 5.6 x 10-10 9.25 4.75 Methylamine, CH;NH2 Dimethylamine, (CH,),NH Ethylamine, C,H;NH, 3.6 x 104 3.44 2.8x 10-1 10.56 2.3x 10-8 7.63 6.37 5.4 x 104 3.27 1.9 x 10-11 10.73 Hypochlorous acid, HCIO Hypobromous acid, HBRO Boric acid, B(OH), 3.3 x 10-7 6.47 3.0 x 10-8 7.53 6.5 x 104 3.19 1.5 x 10-11 10.81 5.0 x 106 5.31 2.0 x 10-9 8.69 Triethylamine, (C,H;);N 1.0 x 10-9 2.99 1.0 x 10-11 11.01 1.4 x 10-5 4.86 7.2 x 10-10 9.14 Strongest weak bases Hydrocyanic acid, HCN Phenol, CgH;OH 2.0x 10-5 4.69 4.9 x 10-10 9.31 7.7 x 10-5 4.11 1.3 x 10-10 9.89 Hypoiodous acid, HIO 4.3 x 104 3.36 2.3 x 10-11 10.64 *Values for polyprotic acids-those capable of donating more than one proton-refer to the first deprotonation. The proton transfer equilibrium is B(OH),(aq) + 2 H,0(1)= H,O*(aq) + B(OH), (aq). Weakest weak acids
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