Issue 18, 1989

Synchronous concerted bond heterolyses in the solvolysis of substituted benzyl azoxyarenesulphonates and characterization of the transition state

Abstract

Hammett parameters[ρ(σx+)=–3.27 and ρ(σY)= 1.07] for the solvolysis of a range of substituted benzyl azoxyarenesulphonates in 1 : 1 (v/v) trifluoroethanol–water indicate that the rate-determining fragmentation is a synchronous concerted process.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1358-1360

Synchronous concerted bond heterolyses in the solvolysis of substituted benzyl azoxyarenesulphonates and characterization of the transition state

I. M. Gordon and H. Maskill, J. Chem. Soc., Chem. Commun., 1989, 1358 DOI: 10.1039/C39890001358

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