Issue 16, 1979

Mechanism in sulphonyl group transfer: effective charge in ground-, transition-, and product-states during base-catalysed hydrolysis of aryl sulphonate esters possessing associative (AE) and dissociative (EA) mechanisms

Abstract

Substituent effects on rate and equilibrium constants for transfer of sulphonyl species to phenols lead to measures of the change in effective charge on participating atoms in the transition-state of the rate-limiting step; results are obtained for both dissociative and associative sulphonyl group transfer mechanisms.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 717-719

Mechanism in sulphonyl group transfer: effective charge in ground-, transition-, and product-states during base-catalysed hydrolysis of aryl sulphonate esters possessing associative (AE) and dissociative (EA) mechanisms

S. Thea, M. G. Harun and A. Williams, J. Chem. Soc., Chem. Commun., 1979, 717 DOI: 10.1039/C39790000717

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements