Abstract
A detailed study has been made of the
reactions of di-p-nitrobenzoyl peroxide with p-dichlorobenzene, naphthalene,
and nitrobenzene. The reaction with p-dichlorobenzene gives much higher yields
of substituted diphenyls, than the corresponding reaction with benzoyl
peroxide.
The stoicheiometry of the reaction with
naphthalene is different from that of the benzoyl peroxide-naphthalene system.
Possible mechanisms of the formation of dinaphthyls are discussed.
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