KINETICS AND MECHANISM OF ACID CATALYSIS IN THE MUTAROTATION REACTIONOF N-(P-CHLOROPHENYL)-BETA-D-GLUCOPYRANOSYLAMINE IN METHANOLIC BENZOATE BUFFER SOLUTIONS
K. Smiataczowa et al., KINETICS AND MECHANISM OF ACID CATALYSIS IN THE MUTAROTATION REACTIONOF N-(P-CHLOROPHENYL)-BETA-D-GLUCOPYRANOSYLAMINE IN METHANOLIC BENZOATE BUFFER SOLUTIONS, Polish Journal of Chemistry, 71(6), 1997, pp. 831-839
Rate constants of the mutarotation reaction of N-(p-chlorophenyl)-beta
-D-glucopyranosylamine have been determined in methanolic benzoate buf
fer solutions of various benzoic acid/sodium benzoate molar concentrat
ion ratios, at 25 degrees C. The measurements were repeated in solutio
ns of the same composition at fixed ionic strength. Catalytic constant
s of the hydrogen ions, k(H), and of benzoic acid molecules, k(HA), ha
ve been determined. In the pH range of approx. 7 to 10.5, the reaction
has been found to obey the general acid catalysis scheme.