Substituent Effects on the Activation Parameter Changes for the Aminolysis in the Bimolecular Nucleophilic Reactions in Solution

Variation of the activation parameters for the aminolysis in the S N 2, acyl-transfer, S N Ar and Ad N reactions offers an additive mechanistic tool for the studies of these reactions in solution. This approach uses the substituent effects on the benzene and pyridine rings to the variation of the activation parameters, I” X ≠ ( X = H , S , G ), in the above reactions in the frameworks of the Hammett – like equations in order to evaluate the resultant I´I” X ≠ reaction constants. The single linear dependences of the internal enthalpy constants I´I” H ≠ int on the I´I” G ≠ and the Hammett I constants show that the substituent effects in the leaving and nonleaving groups and nucleophiles on the mechanistic features in aminolysis of bimolecular nucleophilic reactions are governed by the magnitude of I´I” H ≠ int when one of the steps of the process is the single rate-determining step.