Issue 14, 1975

Dipole moments of methyl- and trifluoromethyl-substituted methyl benzoates

Abstract

Apparent dipole moments in benzene of 1,3-bistrifluoromethylbenzene and of the methyl esters of 2,4-dimethyl-,2,5-dimethyl-, 3,5-dimethyl-, 2,4-bistrifluoromethyl-, 2,5-bistrifluoromethyl-, 3,5-bistrifluoromethyl-, and 3-trifluoromethyl- benzoic acid have been determined. The values obtained can be explained either by rotation of the ester group out of the plane of the ring or, in the case of the 3-, and 2,4-substituted esters, by the existence of cis- and trans-isomers.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1975, 1587-1590

Dipole moments of methyl- and trifluoromethyl-substituted methyl benzoates

G. Hallas, J. D. Hepworth, D. A. Ibbitson and D. E. Thornton, J. Chem. Soc., Perkin Trans. 2, 1975, 1587 DOI: 10.1039/P29750001587

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