A COMPARISON OF SUBSTITUENT EFFECTS ON THE STABILITY OF ALPHA,ALPHA-DIMETHYLBENZYL CARBOCATIONS IN AQUEOUS-SOLUTION AND IN THE GAS-PHASE - HOW SIGNIFICANT IS NUCLEOPHILIC SOLVATION

Rate and equilibrium constants for conversion of ring-substituted cumyl alcohols in acidic solutions of 50:50 (v/v) trifluoroethanol/water (I = 0.50, NaClO4) to an equilibrium mixture of the corresponding cumyl alcohol, cumyl trifluoroethyl ether, and alpha-methylstyrene and the fractional yields of cumyl trifluoroethyl ether obtained from partitioning of the cumyl carbocation intermediates of these reactions between capture by water and by trifluoroethanol have been determined. These data and estimates of absolute rate constants for the reaction of ring-substituted cumyl carbocations with water in 50:50 (v/v) trifluoroethanol/water(30) have been used to calculate equilibrium constants K-R and K-p respectively for conversion of ring-substituted cumyl carbocations to the corresponding cumyl alcohols and alpha-methylstyrenes and the changes in Gibbs free energy (Delta G(X))(sol) for deprotonation of ring-substituted cumyl carbocations by alpha-methylstyrene. A plot of (Delta G(X))(sol) against (Delta G(X))(gas) for the corresponding reactions in the gas phase is linear with a slope of 0.70, in contrast to the previously reported unitary slopes of correlations of substituent effects on carbocation stability in solution and in the gas phase. We conclude that there is a modest increase in the stabilization of ring-substituted cumyl carbocations by solvation as their stability is decreased, but that this is much smaller than the change in stabilization by solvation with the changing stability of pyridinium and anilinium ions. The possible relevance of these data to the stabilization of carbocations by nucleophilic solvation is discussed.