The hydrolysis of several ring substituted methyl benzoates was invest
igated in aqueous solution over a pH range of 3-10. Both the pH depend
ence (at pH > 5) and the variation of hydrolysis rates with ring subst
itution are consistent with a mechanism involving the addition of hydr
oxide ion to the ester carbonyl group. Extrapolation of the rate data
to a pH and temperature that would be consistent with soil and groundw
ater (pH 8, 10 degrees C) indicate that these esters could have hydrol
ysis half lives from several months to several years in the environmen
t.