Issue 5, 1973

Iodination and iodo-compounds. Part IV. The effect of substituents and solvent composition on the rate of aromatic iodination by means of the tri-iodine cation

Abstract

The rate and products of the reaction between each of a range of deactivated substituted benzenes and the tri-iodine cation, in sulphuric acid solution, have been investigated. The rate constants may be correlated by the electrophilic substituent constants σ+ giving a value for the reaction constant ρ=–6·4. The kinetic isotope effect for the iodination of benzoic acid was found to be kH/kD= 2. Further details of the solvent effect are reported.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1973, 595-599

Iodination and iodo-compounds. Part IV. The effect of substituents and solvent composition on the rate of aromatic iodination by means of the tri-iodine cation

J. Arotsky, A. C. Darby and J. B. A. Hamilton, J. Chem. Soc., Perkin Trans. 2, 1973, 595 DOI: 10.1039/P29730000595

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