Reactivity of ethylenic compounds: bromination reaction. Solvation and charge development in the transition state of Ad E C1 mechanism in hydroxylic solvents

Abstract
An analysis of the secondary solvent isotope effect and of the solvent effect in methanol–water mixtures on the rate of bromination of pent-1-ene indicates that the transition state for this reaction is highly polarized and essentially solvated through hydrogen bonding.

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