The rate constants for the reaction of 2,6‐bis(trifluoromethanesulfonyl)‐4‐nitroanisole with some substituted anilines have been measured by spectrophotometric methods in methanol at various temperatures. The data are consistent with the SNAr mechanism. The effect of substituents on the rate of reaction has been examined. Good linear relationships were obtained from the plots of log k1 against Hammett σpara constants values at all temperature with negative ρ values (−1.68 to −1.11). Activation parameters Δ≠H varied from 41.6 to 54.3 kJ mol−1 and Δ≠S from −142.7 to −114.6 J mol−1 K−1. The δΔ≠H and δΔ≠S reaction constants were determined from the dependence of Δ≠H and Δ≠S activation parameters on the σ substituent constants, by analogy with the Hammett equation. A plot of Δ≠H versus Δ≠S for the reaction gave good straight line with 177°C isokinetic temperature. © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 203–210, 2010