Issue 10, 1970

Intramolecular hydrogen bonding in protonated α-halogeno-aldehydes: nuclear magnetic resonance study

Abstract

The n.m.r. spectra of protonated α-chloroacetaldehyde and α-chlorobutyraldehyde in strong acid solution show the presence of two isomeric species, one of which can be explained in terms of intramolecular hydrogen bonding between the proton on oxygen and the chlorine atom.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 591-592

Intramolecular hydrogen bonding in protonated α-halogeno-aldehydes: nuclear magnetic resonance study

L. Thil, J. J. Riehl, P. Rimmelin and J. M. Sommer, J. Chem. Soc. D, 1970, 591 DOI: 10.1039/C29700000591

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