{"title":"The oxidation of diphenylhydroxylamine by benzoyl peroxide","authors":"G. R. Chalfont, M. Perkins","doi":"10.1039/J29710000245","DOIUrl":null,"url":null,"abstract":"In the presence of a large excess of diphenylhydroxylamine the title reaction gives benzoic acid and diphenyl nitroxide according to the equation 2Ph2NOH +(PhCO2)2→ 2Ph2NO·+ 2PhCO2H. The reaction is of the first order in both peroxide and hydroxylamine. Although this is one of the most clear-cut examples of molecule-induced homolysis known, no convincing evidence has been adduced in favour of any one mechanism. Substituent and isotope effects are consistent with an initial electron transfer from hydroxylamine to peroxide.","PeriodicalId":17268,"journal":{"name":"Journal of The Chemical Society B: Physical Organic","volume":"457 1","pages":"245-249"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society B: Physical Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J29710000245","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
In the presence of a large excess of diphenylhydroxylamine the title reaction gives benzoic acid and diphenyl nitroxide according to the equation 2Ph2NOH +(PhCO2)2→ 2Ph2NO·+ 2PhCO2H. The reaction is of the first order in both peroxide and hydroxylamine. Although this is one of the most clear-cut examples of molecule-induced homolysis known, no convincing evidence has been adduced in favour of any one mechanism. Substituent and isotope effects are consistent with an initial electron transfer from hydroxylamine to peroxide.