Abstract
Disulphides catalytically break down tert-butyl and cumyl hydroperoxides. In chlorobenzene breakdown takes place by a bimolecular mechanism at a rate which is directly proportional to the concentration of hydroperoxide and disulphide; the rate constant of this reaction varies from 0·4 to 1·21.mole · sec at 373°K for disulphides and tert-butyl hydroperoxide, respectively. No radicals are formed by the reaction of tert-butyl hydroperoxide with disulphide.
Published Version
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