Ethylene/alpha -olefin copolymers having bimodal molar weight distribution are investigated in comparison with unimodal copolymers in order to understand the incidence of the molecular architecture on the stress cracking resistance. The preferred introduction of the co-units in the longest chains of bimodal copolymers is suggested to favour the occurrence of intercrystalline tie molecules during crystallisation. The more complex is the molecular architecture, the greater is the difficulty for crystallisation by regular chain folding. Intermolecular chemical heterogeneity resulting from preferred incorporation of the co-units in the long chains enhances the co-unit disturbing effect on crystallisation without reducing crystallinity. Intra-molecular heterogeneity of the co-unit distribution is also suggested to be an efficient means to generate tie molecules and random chain folding at the expense of regular chain folding. Isothermal crystallisation is used to probe the effect of molecular architecture on the crystallisation kinetics. It appeared that the correlations between kinetics, molecular architecture and molecular topology of unimodal copolymers no longer hold when considering bimodal copolymers. In contrast, the crystal surface free energy proved to be sensitive to topological changes resulting from molecular architecture modifications.