Issue 10, 1975

Predominant ortho-substitution in the gas-phase attack of the t-butyl cation on m-xylene

Abstract

The gas-phase attack of radiolytically formed t-butyl cation on m-xylene yields over 65% of the 1,3-dimethyl-4-t-butyl isomer under conditions favouring kinetic control of products, while a significant proportion of 1,3-dimethyl-5-t-butylbenzene is formed as the pressure is lowered from 760 to 20 Torr.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 379-380

Predominant ortho-substitution in the gas-phase attack of the t-butyl cation on m-xylene

P. Giacomello and F. Cacace, J. Chem. Soc., Chem. Commun., 1975, 379 DOI: 10.1039/C39750000379

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