Polymerizations and mechanistic studies have been performed to understand the kinetic pathways for the polymerization of the monomer oligo(ethylene oxide) monomethyl ether acrylate (OEOA) in aqueous media. Typically, the medium consisted of 18 wt % OEOA in water, in the presence of Cu catalysts coordinated by tris[2(dimethylamino)ethyl] amine (Me6TREN). Well-controlled polymerization of OEOA can be achieved in the presence of halide anions and Cu wire with less than or similar to 600 ppm of soluble Cu-II species, rather than previously reported ca. 10 000 ppm of Cu-II and Cu-0 particles formed by predisproportionation of Cu-I prior to monomer and initiator addition. The mechanistic studies conclude that even though disproportionation is thermodynamically favored in aqueous media, the SARA ATRP, not SET-LRP, mechanism holds in these reactions. This is because alkyl halides are much more rapidly activated by Cu-I than by Cu-0 (contribution of Cu-0 to activation is <1%). Because of the high activity of Cu-I species toward alkyl halide activation, [Cu-I/Me6TREN] in solution is very low (<5 mu M) and classical ATRP equilibrium between Cu-I and Cu-II species is maintained. Although in aqueous media disproportionation of Cu-I/Me6TREN is thermodynamically favored over comproportionation, unexpectedly, in the presence of alkyl halides, i.e., during polymerization, disproportionation is kinetically minimized. Disproportionation is slow because its rate is proportional to [Cu-I/Me6TREN]2 and [Cu-I/Me6TREN] is very small. Thus, during polymerization, comproportionation is 10(4) times faster than disproportionation, and the final thermodynamic equilibrium between disproportionation and comproportionation could be reached only after polymerization is completed. Activation of alkyl halides by Cu-I/Me6TREN in aqueous media occurs 8 orders of magnitude faster than disproportionation.