Pseudo-first-order rate constants have been determined for the nucleophilic substitution reactions of p-nitrophenyl acetate with p-chlorophenoxide (4-ClC 6 H 4 O − ) and N-phenylbenzohydroxamate (C 6 H 5 CON(C 6 H 5 )O − ) ions in phosphate buffer (pH 7.7) at 27 • C. The effect of cationic, (CTAB, TTAB, DTAB), anionic (SDS), and nonionic (Brij-35) surfactants has been studied. The k obs value increases upon addition of CTAB and TTAB. The effect of DTAB and other surfactants on the reaction is not very significant. The micellar catalysis and α-effect shown by hydroxamate ion have been explained.