Appendix B - Acidity Constants for Some Organic Compounds
- Page ID
- 507275
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\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)| Compound | pKa |
|---|---|
| CH3SO3H | −1.8 |
| CH(NO2)3 | 0.1 |
| 0.3 | |
| CCl3CO2H | 0.5 |
| CF3CO2H | 0.5 |
| CBr3CO2H | 0.7 |
|
|
1.2; 2.5 |
| HO2CCO2H | 1.2; 3.7 |
| CHCl2CO2H | 1.3 |
| CH2(NO2)CO2H | 1.3 |
|
|
1.9 |
|
(Z) |
1.9; 6.3 |
| 2.4 | |
| CH3COCO2H | 2.4 |
| NCCH2CO2H | 2.5 |
|
|
2.6 |
| CH2FCO2H | 2.7 |
| CH2ClCO2H | 2.8 |
| HO2CCH2CO2H | 2.8; 5.6 |
| CH2BrCO2H | 2.9 |
| 3.0 | |
| 3.0 | |
| CH2ICO2H | 3.2 |
| CHOCO2H | 3.2 |
| 3.4 | |
| 3.5 | |
| HSCH2CO2H | 3.5; 10.2 |
| CH2(NO2)2 | 3.6 |
| CH3OCH2CO2H | 3.6 |
| CH3COCH2CO2H | 3.6 |
| HOCH2CO2H | 3.7 |
| HCO2H | 3.7 |
| 3.8 | |
| 4.0 | |
| CH2BrCH2CO2H | 4.0 |
| 4.1 | |
| 4.2 | |
|
|
4.2 |
| HO2CCH2CH2CO2H | 4.2; 5.7 |
| HO2CCH2CH2CH2CO2H | 4.3; 5.4 |
| 4.5 | |
|
|
4.7 |
| CH3CO2H | 4.8 |
| CH3CH2CO2H | 4.8 |
| (CH3)3CCO2H | 5.0 |
| CH3COCH2NO2 | 5.1 |
| 5.3 | |
| O2NCH2CO2CH3 | 5.8 |
| 5.8 | |
| 6.2 | |
| 6.6 | |
| HCO3H | 7.1 |
| 7.2 | |
| (CH3)2CHNO2 | 7.7 |
| 7.8 | |
| CH3CO3H | 8.2 |
| 8.5 | |
| CH3CH2NO2 | 8.5 |
| 8.7 | |
| CH3COCH2COCH3 | 9.0 |
| 9.3; 11.1 | |
| 9.3; 12.6 | |
| 9.4 | |
| 9.9; 11.5 | |
| 9.9 | |
| CH3COCH2SOCH3 | 10.0 |
| 10.3 | |
| CH3NO2 | 10.3 |
| CH3SH | 10.3 |
| CH3COCH2CO2CH3 | 10.6 |
| CH3COCHO | 11.0 |
| CH2(CN)2 | 11.2 |
| CCl3CH2OH | 12.2 |
| Glucose | 12.3 |
| 12.4 | |
| CH2(CO2CH3)2 | 12.9 |
| CHCl2CH2OH | 12.9 |
| CH2(OH)2 | 13.3 |
| HOCH2CH(OH)CH2OH | 14.1 |
| CH2ClCH2OH | 14.3 |
| 15.0 | |
| 15.4 | |
| CH3OH | 15.5 |
| 15.5 | |
| CH3CH2OH | 16.0 |
| CH3CH2CH2OH | 16.1 |
| CH3COCH2Br | 16.1 |
| 16.7 | |
| CH3CHO | 17 |
| (CH3)2CHCHO | 17 |
| (CH3)2CHOH | 17.1 |
| (CH3)3COH | 18.0 |
| CH3COCH3 | 19.3 |
| 23 | |
| CH3CO2CH2CH3 | 25 |
|
|
25 |
| CH3CN | 25 |
| CH3SO2CH3 | 28 |
| (C6H5)3CH | 32 |
| (C6H5)2CH2 | 34 |
| CH3SOCH3 | 35 |
| NH3 | 36 |
| CH3CH2NH2 | 36 |
| (CH3CH2)2NH | 40 |
| 41 | |
| 43 | |
| 44 | |
| CH4 | ∼60 |
An acidity list covering more than 5000 organic compounds has been published: E.P. Serjeant and B. Dempsey (eds.), “Ionization Constants of Organic Acids in Aqueous Solution,” IUPAC Chemical Data Series No. 23, Pergamon Press, Oxford, 1979.


