Abstract
In an investigation on the effect of branching in the γ‐position of alkyl and cycloalkyl halides and arylsulfonates the solvolysis rates and products of cis‐ and trans‐3,3,5‐trimethylcyclohexyl tosylate (18) and (19), 1‐bromo‐ and 1‐bromo‐3,3‐dimethyl‐bicyclo[2.2.2]octane (20a and b), 1‐bromo‐adamantane (21a) and its 3‐methyl, 3‐ethyl, 3‐isopropyl and 3,5,7‐trimethyl derivatives (21b, c, d) and (22), respectively, have been determined.

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