Structure and Reactivity. I. The Oximation Rates of Some Straight-Chain and Monomethyl-Substituted Alkanones
PG Kletzke
Index: Kletzke,P.G. Journal of Organic Chemistry, 1964 , vol. 29, p. 1363 - 1366
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Citation Number: 10
Abstract
'The oxinration rates have been determined for 65 straight-chain and monomethyl- substituted alkanones. The methyl ketones are the most reactive of the straight-chain ketones studied, followed by the ethyl ketones, The propyl and higher ketones have the same rate. A methyl group on the first carbon adjacent to the carbonyl group lo\ rers the rate the most as compared to the corresponding straight-rhain cwrnpounds. This decreased ...
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