Abstract
Solvent effects on reaction
constant ρ for the dissociation equilibria of several series of organic acids
are analysed in terms of three factors, namely, (i)
variation in the effective dielectric constant, (ii) variation in the
hydrogen-bonding ability of solvents, and (iii) variation in the conformation
of the acids. A fourth factor, variation in the charge developed in the
transition state of the reaction, is included in the analysis of ρ for
reactions between diazodiphenylmethane and several series of carboxylic acids.
It is shown that the ρ values for the dissociation equilibria of series of
acids in other solvents can be calculated from their ρ values in water.
Cited by
6 articles.
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