Issue 11, 1972

The mechanism of nitration of 2,3-dinitroaniline in aqueous sulphuric acid. Evidence for Bamberger's hypothesis of N-nitration followed by rearrangement

Abstract

Product analyses and tracer studies involving H15NO3 show that the 6-nitration of 2,3-dinitroaniline by nitric acid in aqueous sulphuric acid occurs mainly by attack on the amino nitrogen atom followed by rearrangement.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 641-641

The mechanism of nitration of 2,3-dinitroaniline in aqueous sulphuric acid. Evidence for Bamberger's hypothesis of N-nitration followed by rearrangement

J. H. Ridd and E. F. V. Scriven, J. Chem. Soc., Chem. Commun., 1972, 641 DOI: 10.1039/C39720000641

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