Issue 0, 1966

Molecular polarisability and internal rotation in the alkyl chloride series

Abstract

The molar Kerr constants and dipole moments, measured at infinite dilution in carbon tetrachloride, of t-butyl, ethyl, n-propyl, n-butyl, n-pentyl, and n-hexyl chloride are recorded. Inductive effects in these molecules are briefly discussed. Estimates of the anisotropic polarisability of the C–Cl bond in t-butyl and ethyl chloride are obtained. Molar Kerr constants of the n-alkyl chlorides lie in the range +56 to 62 × 10–12. Expectation values of the molar Kerr constants, obtained by a treatment previously applied to n-alkyl bromides and iodides, are in excellent agreement with experiment. For n-propyl chloride, the gauche–trans energy difference is found to be +0·14± 0·1 kcal./mole.

Article information

Article type
Paper

J. Chem. Soc. B, 1966, 37-40

Molecular polarisability and internal rotation in the alkyl chloride series

R. J. W. Le Fèvre and B. J. Orr, J. Chem. Soc. B, 1966, 37 DOI: 10.1039/J29660000037

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