Name Structure NH; CHCH, 2.20 (CO,H) 9.31 (NH3) 6.3 X 10-3 4.9 x 10-10 Phenylalanine ČO,H 2.148 * 7.198 · 12.375 7.11 × 10-3 6.34 x 10-8 4.22 X 10-13 Но — Р- Н Phosphoric acid* (hydrogen phosphate) OH (1.5) 6.78 3 x 10-2 1.66 х 10-7 НР — ОН Phosphorous acid (hydrogen phosphite) OH
Name Structure NH; CHCH, 2.20 (CO,H) 9.31 (NH3) 6.3 X 10-3 4.9 x 10-10 Phenylalanine ČO,H 2.148 * 7.198 · 12.375 7.11 × 10-3 6.34 x 10-8 4.22 X 10-13 Но — Р- Н Phosphoric acid* (hydrogen phosphate) OH (1.5) 6.78 3 x 10-2 1.66 х 10-7 НР — ОН Phosphorous acid (hydrogen phosphite) OH
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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
Transcribed Image Text:Structure
pK,
K.
Name
NH;
CHCH,-O
2.20 (СО,Н)
9.31 (NH,)
6.3 X 10-3
4.9 x 10-10
Phenylalanine
CO,H
7.11 x 10-3
6.34 x 10-8
2.148
* 7.198
Phosphoric acid*
(hydrogen phosphate)
НО — Р— Он
12.375
4.22 X 10-13
OH
(1.5)
6.78
3 x 10-2
1.66 x 10-7
HP-
он
Phosphorous acid
(hydrogen phosphite)
OH
1.12 x 10-3
3.90 x 10-6
2.950
Phthalic acid
(benzene-1,2-dicarboxylic acid)
5.408
cO,H
Piperazine
(perhydro- 1,4-diazine)
5.333
9.731
4.65 x 10-6
1.86 X 10-10
11.125
7.50 x 10-12
Piperidine
1.12 x 10-2
2.29 x 10-11
-co,H
1.952 (СO,Н)
10.640 (NH,)
Prolinc
+H
4.874
1.34 x 10-5
Propanoic acid
CH,CH,CO,H
H,C=CHCO,H
4.258
5.52 x 10-5
Propenoic acid
(аcrylic acid)
10.566
2.72 x 10-11
Propylamine
CH;CH,CH,NII;
5.20
6.3,X 10-6
Pyridine
(azine)
Pyridine-2-carboxylic acid
(picolinic acid)
(1.01) (CO,H)
5.39 (NH)
9.8 x 10-2
4.1 x 10-6
co,H
HO,C
Pyridine-3-carboxylic acid
(nicotinic acid)
2.03 (CO,H)
4.82 (NH)
9.3 x 10-3
1.51 x 10-s
NH+
1.4 (POH) (u = 0.1)
3.44 (OH) (1p. = 0.1)
6.01 (POH) (u = 0.1)
8.45 (NH) (u = 0.1)
0.04
3.6 x 10-4
9.8 x 10-7
3.5 x 10-9
0=CH
Pyridoxal-5-phosphate
Но — РОСН,
но
`CH,
H.
0.15
5.5 X 10-3
1.9 X 10-7
3.5 X 10-10
Pyrophosphoric acid
(hydrogen diphosphate)
0.83
2.26
(HO),POP(OH),
6.72
9.46
*pK, from A. G. Miller and J. W. Macklin, Anal. Chem. 1983, 55, 684.
APPENDIX G Acid Dissociation Constants
АP18
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