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High pressure kinetics appears to be a valuable tool in investigating the mechanism of specific organic reactions. For instance, in pericyclic, Mentshutkin, cage, and polymerization reactions, such studies reveal various features of the transition state, in particular its localization along the reaction coordinate and its nature. However, precise conclusions require separation of the different effects (electrostatic, steric, orbital, etc.) which may contribute to the structure of the transition state.
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Gérard Jenner (1975) studied this question.
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