Abstract

The rate constants for the reactions of some 3-substituted 2-thenoyl chlorides (I; X = OMe, Me, SMe, H, I, Br, SOMe, and SO2Me) with aniline in benzene have been measured. A plot of the logarithm of the rate constants versus the –ΔpKa values of the corresponding acids furnishes an example of a non-linear free energy relationship, indicating the occurrence of different reaction mechanisms for 2-thenoyl chlorides with, respectively, electron-attracting and -repelling substituents at C-3.

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