Influence of sulfur groups on carboxylic acid strengths
Author:
Funder
Indiana University Foundation
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Presented, in part, before the ACS Meeting-in-miniature,1971
2. For example, the pKa values for acetic acid decrease with chlorine substitution: CH3COOH pKa = 4.75; CH2ClCOOH pKa = 2.85; CHCl2COOH pKa = 1.48; and CCl3COOH pKa = 0.704a.
3. Some evidence of β-ketosulfoxide metal coordination
4. Handbook of Chemistry and Physics,1969
5. CCXCIV.—Electrometric titration curves of dibasic acids. Part IV. Corrections for interionic effects and for solvent electrostriction. First and second dissociation constants of some n-paraffin αω-dicarboxylic acids, alkyl- and dialkyl-malonic acids, s-di- and -tetra-alkylsuccinic acids, β-alkyl-and ββ-dialkyl-glutaric acids, and cyclic 1 : 1-di-acetic acids. Remarks on the configurations and molecular dimensions of these acids in dilute aqueous solution
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