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Mechanisms of nucleophilic substitution. Kinetics of the reactions of benzyl and diphenylmethyl chlorides in aqueous acetone
Journal of the Chemical Society D: Chemical Communications Pub Date : , DOI:10.1039/C29710000797
Abstract

The unified mechanism of nucleophilic substitution cannot account for the present observations on the rates of decomposition of benzyl and diphenylmethyl chlorides in aqueous acetone; this also applies to any extension of the unified mechanism which does not include carbonium ions as intermediates (mechanism SN1) and a separate reaction path involving direct nucleophilic attack on the substrate (mechanism SN2).

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