Abstract
The structures assigned to the 4-aminocyclohexanols have been confirmed and some fundamental reactions studied. Solvolysis of trans-4-benzamidocyclohexyl toluene-p-sulphonate has shown absence of participation in the rate-determining step although product analysis indicates that the reaction proceeds with retention of configuration. The bromination of 4-benzamidocyclohexene and solvolysis of the products have been studied.

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