Issue 7, 1978

The reactivity of 2-bromo-1-phenylethanone (phenacyl bromide) toward nucleophilic species

Abstract

A comparison of second-order rate constants for reactions of 2-bromo-1-phenylethanone (phenacyl bromide) and methyl iodide with various nucleophiles in acetonitrile at 25·0 °C reveals that the rate enhancement due to the carbonyl group in the position adjacent to the reacting carbon atom in alkyl halides is not a general effect but is very dependent upon the nucleophile.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 327-328

The reactivity of 2-bromo-1-phenylethanone (phenacyl bromide) toward nucleophilic species

A. Halvorsen and J. Songstad, J. Chem. Soc., Chem. Commun., 1978, 327 DOI: 10.1039/C39780000327

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