1-(1-Methyl-2-pyrrolyl)-2, 2, 2-trifluoroethyl p-nitrobenzoate (3) reacts by carbocation formation with an m value for the dependence of rate on the solvent polarity parameter Y OTs of 0.56, and a rate 41 times slower than (1-methyl-2-pyrrolyl) methyl p-nitrobenzoate. The products from 3 include significant amounts of material derived from solvent attack at the 5-position of the pyrrole ring. The results indicate a high degree of charge delocalization ...