Studies on the Autoxidation of Phenyl Cycloalkanes

Abstract The products of the autoxidation of phenyl cyclopropane (I), phenyl cyclobutane (II), phenyl cyclopentane (III), phenyl cyclohexane (IV), phenyl cycloheptane (V) and phenyl cyclooctane (VI) were analyzed after reduction of the reaction mixtures with LiAlH4. As products of the attack on the α‐CH bonds the corresponding 1‐phenyl cycloalkanols and 1‐phenyl alkan‐1‐ols were found. In the case of phenyl cyclopropane some SR2 ring opening probably takes place. The oxidabilities \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm k}_{\rm p} /\sqrt {{\rm k}_{\rm t}} $\end{document} , the chain termination constants kt, the absolute chain propagation constants kp and the relative chain propagation constant (kp)rel were determined for the phenyl cycloalkanes I—VI. As it is to be expected on the basis of the I‐strain concept the autoxidation rate of phenyl cyclopentane (III) is considerably higher than that of phenyl cyclobutane (II) and phenyl cyclohexane (IV).