Kinetics of oxidation of five vicinal, four non-vicinal diols, and one of their monoethers by pyridinium hydrobromide perbromide (PHPB) have been studied. The vicinal diols yield products arising out of the glycol bond fission while the other diols yield hydroxyca/'bonyl compounds. The reaction is first order with respect to PHPB. Michaelis-Menten type kinetics are observed wih respect to the diol. There is no effect of added pyridinium bromide on the reaction. The oxidation of [1, 1,2, 2-2H,]ethanediol shows the absence of a primary kinetic isotope effect. The values of solvent isotope effect, k(HzO)/k(D20), at 313 K, for the oxidation of ethanediol, propane-l, 3-dioi and 3-methoxybutan-l-ol are 4.71, 2-17 and 2.23 respectively. A mechanism involving glycol-bond fission has been proposed for the oxidation of the vicinal diols. The other diois are oxidised by a hydride-transfer mechanism as they are monohydric alcohols.