SUMMARY: Copolymerizations of several isopropylidene-protected vinyl sugars with styrene, methyl methacrylate, and acrylonitrile were carried out in solution and in bulk. Reactivity ratios of the vinyl sugars with these comonomers (ratio of the rate constant for adding its own monomer to that for adding the other monomer) were determined. Copolymers with varying composition were obtained. After eliminating the hydrophobic protecting groups from the copolymer surfaces by acid hydrolysis, these surfaces become hydrophilic owing to newly formed hydroxyl groups. This heterogeneous reaction is carried out on samples in the form of plates, films, or powders. Water contact angle measurements clearly showed the hydrophilic properties of surfaces and the removal of isopropylidene groups from the surfaces. X-ray photoelectron spectroscopy (XPS) demonstrated the change of the chemical surface composition. Dyeability and surface conductivity of the copolymers were improved by forming OH groups at the surfaces. Vinyl sugars with C1C linkages between vinyl groups and sugar segments had a better stability to treatment with hydrochloric acid than those with ester linkages. Vinyl sugars with an open-chain structure were more efficient in improving the hydrophilicity of the copolymer surfaces than those with cyclic structures.