Abstract
Product distributions of the OH+D2→HOD+D reaction, calculated using quasi-classical means, on various potential energy surfaces for the rotational states j D 2=0, 1, 2, 3 and 4 of the D2 molecule are compared with those derived from crossed molecular beam experiments with the aim of assessing the validity of the proposed potential energy functionals in describing the reaction channel of the system. Surprisingly, the most accurate surface, while leading to an excellent reproduction of translational and angular product distributions, was found to be unable to reproduce the measured vibrational distribution.
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