Abstract

Substituted S-aryl and O-aryl N-arylthiocarbamates have been synthetized. Kinetic studies of hydrolysis of these compounds in 20% aqueous dioxane prove the E1cB mechanism. The found Hammett reaction constants, activation entropy values, Broensted coefficients, and comparison of reactivity with N-methyl analogues have been discussed as criteria of the mentioned mechanism. Hydrolysis results of thiocarbamates in the same medium are compared.

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