226. Mechanism of electrophilic substitution at a saturated carbon atom. Part III. Kinetics, stereochemistry, and mechanism of the three-alkyl mercury-exchange …

HB Charman, ED Hughes, C Ingold…

Index: Charman, H. B.; Hughes, E. D.; Ingold, C.; Thorpe, F. G. Journal of the Chemical Society, 1961 , p. 1121 - 1133

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Citation Number: 7

Abstract

It is shown that mercury-for-mercury replacement in the reactions of s-butylmercuric bromide, acetate, and nitrate, severally, with di-s-butylmercury in ethanol is the anticipated, but observationally new, three-alkyl substitution, proceeding by the bimolecular electrophilic mechanism SE2, in which stereochemical configuration is fully preserved. That this threealkyl electrophilic exchange is indeed under observation, rather than any other ...