Issue 8, 1973

Bromopicrin reaction. Part II. Reaction between 2-nitroethanol and sodium hypobromite

Abstract

Reaction between 2-nitroethanol and sodium hypobromite gives bromopicrin (CBr3NO2) in high yield. A kinetic study indicates that 2,2-dibromo-2-nitroethanol is an intermediate and that the rate-determining step is proton removal from 2-nitroethanol.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1973, 1107-1110

Bromopicrin reaction. Part II. Reaction between 2-nitroethanol and sodium hypobromite

R. I. Aylott, A. R. Butler, D. S. B. Grace and H. McNab, J. Chem. Soc., Perkin Trans. 2, 1973, 1107 DOI: 10.1039/P29730001107

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