Issue 3, 1989

Kinetics and mechanism of the sodium–ammonia reduction of 2,2,4,4-tetramethylpentan-3-one

Abstract

The kinetics of the reaction of sodium with 2,2,4,4-tetramethylpentan-3-one (TMP) in liquid ammonia was studied using the stopped-flow technique. The reactions were found to obey the fourth-order rate law –d[eam]/dt= 2k[eam]2[ketone][Na+]. The reaction rate was markedly reduced by addition of 2,2,2-cryptand. The addition of a weak acid (ethanol) had no effect on the observed rate. A mechanism involving ion-pairing with dianion formation being the rate-determining step is suggested. When TMP was initially exposed to an excess of lithium amide in liquid ammonia, the resulting mixture was found not to react with the ammoniated electron.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1989, 269-273

Kinetics and mechanism of the sodium–ammonia reduction of 2,2,4,4-tetramethylpentan-3-one

W. M. Song and R. R. Dewald, J. Chem. Soc., Perkin Trans. 2, 1989, 269 DOI: 10.1039/P29890000269

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