Polystyrene and polyacenaphthylene supports were functionalized to generate a t-butyl chromate function and the resulting polymer-supported reagents were used for the oxidation of alcohols. They were found to oxidize primary and secondary alcohols to the corresponding carbonyl compounds in quantitative yields. Oxidation of differently substituted alpha-phenylethanols was attempted for this purpose and the kinetics of oxidation reactions was studied. The reaction was found to be first order with respect to the substrate, the reaction being carried out with an excess of the t-butyl chromate reagent. The rate of oxidation was also found to be dependent on the nature of the substrate, concentration of the reagent function, and the nature and concentration of the acid catalyst used.