Journal of the Chemical Society. Perkin transactions II p. 443 - 448 (1995)
Update date:2022-08-03
Topics:
Atherton, John H.
Crampton, Michael R.
Duffield, Gaynor L.
Stevens, J. Andrew
Rate and equilibrium measurements are reported for the reactions in methanol of carbanions derived from 12 ring-substituted benzyl cyanides with 1,3,5-trinitrobenzene to give ?-adducts.Some data for reaction of the carbanions with 4-nitrobenzofuroxan were also measured.With increasing carbanion reactivity, rate constants approach a limit of just below 109 dm3 mol-1 s-1.Intrinsic reactivities of carbanions in ?-adduct forming reactions and in proton transfer reactions are compared.
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