The statistical copolymerization of isoprene with p-ethyl- (p-ES), p-isopropyl- (p-iPS), and p-tert-butylstyrene (p-tBS) initiated by sec-butyllithium in cyclohexane was investigated with respect to kinetics, reactivity ratios, and formation of tapered block copolymers with pronounced monomer gradient. An efficient synthetic route to the monomers was developed on a multigram scale, relying on the precipitation of the side-product triphenylphosphine oxide at low temperature. The copolymerization kinetics and resulting molecular weight distributions were analyzed. The dispersity, Đ, of the copolymers depends on the p-alkyl substituent, the the degree of polymerization Pn and the comonomer mole fraction, X. In situ 1H NMR kinetics characterization revealed a strong gradient structure for all three copolymer systems (rI = 21.9, rp-ES = 0.022; rI = 19.7, rp-iPS = 0.027; rI = 19.8, rp-tBS = 0.022). The rate of crossover from a polyisoprenyllithium chain end (I) to a p-alkylstyrene (S) unit relative to the alkyl...