Kinetic isotope effects on specific acid-catalyzed protonation of ring-substituted alpha-methoxystyrenes in 50/50 (v/v) H2O/D2O were calculated from the yields of the alpha-CH3 and alpha-CH2D groups at the ring-substituted acetophenone product, determined by H-1 NMR analysis and using phi(H) = 0.69 for fractionation of deuterium between L2O and L3O+. There is a small change in the kinetic isotope effect from 5.6 for protonation of 4-methoxystyrene to 5.0 for protonation of 3,5-dinitrostyrene as the driving force for proton transfer is changed by 9.0 kcal/mol. The intercepts of Arrhenius-type plots of the product isotope effects for protonation of these two styrenes, (A(H)/A(D)) = 1.00 and 0.95, are consistent with a semiclassical model for proton transfer in which there is minimal tunneling of the transferred hydron through the reaction barrier at T = 278-359 K.