The dependence of the conformational rigidity of a copolymer on its co
mposition is studied by computer simulation under the assumption of un
hindered rotation. Random and regular block cyclochain copolymers are
considered. It is shown that rigidity of a copolymer depends not only
on the relative concentrations and geometry of the constituent monomer
units, but also on their distribution in the chain, the rigidity of r
egular block copolymers being higher the longer the blocks. The result
s of calculations for random copolymers contradict those calculated ac
cording to the additive scheme.