Autor: |
Skvortsova, G. G., Mansurov, Yu. A., Deriglazov, N. M. |
Zdroj: |
Chemistry of Heterocyclic Compounds; January 1974, Vol. 10 Issue: 1 p27-29, 3p |
Abstrakt: |
The kinetics of the alkaline hydrolysis of vinyl esters of furan-2-carboxylic, trans-ß-(2-furyl)acrylic, and trans-cinnamic acids and also the comparative electrochemical activities of these compounds and of vinyl esters of 5-bromofuran-2-carboxylic, 5-nitro-furan-2-carboxylic, and benzoic acids have been studied by a polarographic method. A symbatic increase in the rate of hydrolysis of the esters with a shift of the potential of the half-wave of reduction into the more negative region has been established. Both the polarity and the polarizability of the molecules have a fundamental influence on the properties of the esters. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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