Kinetic hydrogen isotope effects in the ionization of some carbon acids

Abstract

Rate constants in aqueous solutions are reported for proton and deuteron abstraction by a variety of bases from tricarbomethoxymethane, the propan-2-one-1-sulphonate ion, 2-acetylcyclohexanone and ethyl nitroacetate. The rates of ionization were measured by using bromine or iodine as scavengers to remove the anions, and, for ethyl nitroacetate by direct observation of the rate of appearance of the anion. The kinetic isotope effects vary from k H / k D = 2.5 to k H / k D = 10.3, and confirm the regularities previously found (Bell & Crooks 1965; Bell & Goodall 1966). In particular, the results for the reaction of ethyl nitro-acetate with nine bases show clearly that with increasing basic strength the isotope effect passes through a well-marked maximum. Sterically hindered pyridine bases give rise to abnormally high isotope effects, probably attributable to increased tunnel corrections.