The composition and stereochemical configuration of methyl methacrylate‐styrene copolymers obtained in benzene, chlorobenzene and benzonitrile has been evaluated by 1H‐NMR spectroscopy. The methyl methacrylate centered triad fractions in the copolymers have been calculated on the basis of the previously reported methoxy signal assignments. The results obtained are discussed taking into consideration the variation in the polarity of solvents; they make it possible to state that the presence of solvents not only affects the kinetic parameters but also changes the composition and the stereochemical configuration of monomer sequences in the copolymers.