Issue 0, 1970

A nitrogen isotope effect study of an aromatic nucleophilic substitution reaction

Abstract

Hydrolysis of p-nitroaniline in aqueous sodium hydroxide was found to be second order with an activation energy of 17 kcal./mole and an entropy of activation of ca.–33 e.u. Absence of a significant nitrogen isotope effect for the reaction established that C–N bond stretching was unimportant in the rate-determining transition state.

Article information

Article type
Paper

J. Chem. Soc. B, 1970, 738-739

A nitrogen isotope effect study of an aromatic nucleophilic substitution reaction

G. Ayrey and W. A. Wylie, J. Chem. Soc. B, 1970, 738 DOI: 10.1039/J29700000738

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