Abstract

The rate of ring inversion and conformational equilibration of 5,5-difluoro-cis-hydrindahn as been determined from the temperature dependence of its fluorine magnetic resonance spectrum. The activation energy for ring inversion was found to be 6.9 ± 0.2 kcal/mol. Introduction of an angular methyl group at the 9 position resulted in an increase in the activation energy to 8.1 ± 0.3 kcal/mol.

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