[en] In this work, we invoke the mechanistic criteria based on the sign of cross-interaction constants, ρ_XY where X and Y are the substituents in the nucleophile and substrate, respectively; for a stepwise mechanism the sign of ρ_XY was invariably positive and the reactivity-selectivity principle (RSP) was found to hold. Although there is abundant literature on the kinetics and mechanism of the aminolysis of aryl carbonates and esters, the aminolysis reactions of aryl carbamates have been less studied in terms of kinetics. The mechanism of the aminolysis of substituted diphenyl carbonates has been studied, and structure-reactivity relationships for those reactions have also been examined in detail by Gresser and Jencks. Castro and co-workers have reported a number of mechanistic studies on the aminolysis of aryl carbonates and esters. These and other studies showed that most of the aminolysis of aryl carbonates and esters proceed by either a stepwise mechanism through a zwitterionic tetrahedral intermediate, T^±, or a concert mechanism depending on the amine, substrate, and solvent involved