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dc.contributor.advisorScholl, P. C.
dc.creatorVan de Mark, Michael Roy
dc.date.accessioned2020-08-21T21:47:34Z
dc.date.available2020-08-21T21:47:34Z
dc.date.issued1976
dc.identifier.urihttps://hdl.handle.net/1969.1/DISSERTATIONS-508797
dc.descriptionVita.en
dc.description.abstractThe remote oxidation of unactivated carbon-hydrogen bonds by photo-excited nitrobenzene and benzophenone derivatives is described. The procedure is illustrated by the key step in the conversion of 5α-androstand-3α-of to 5α-androst-14-en-3-one. The photolysis of benzophenone solubilized in a micell produces some selectivity for the w-position in a 16 carbon micelle. The electrochemical oxidation of aliphatic alcohols has been studied. It was found that acetonitrile and fluoroborate is the best solvent electrolyte system for the direct oxidation of alcohols. The indirect oxidation of secondary alcohols was accomplished in 1:10 water: acetonitrile as the solvent and nitrate as the electro-active species. The direct oxidation of alcohols produced the respective alkoxyl radicals. With isoborneol, the radical undergoes β-fragmentation in high yields. The indirect oxidation with nitrate produced ketones in very high yield from the corresponding secondary alcohol. The mechanistic conclusions derived from these observations were; that the alkoxyl radical was formed, and the subsequent chemistry follows that of the photochemically generated radical.en
dc.format.extentx, 168 leavesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectElectrolytic oxidationen
dc.subjectRadicals (Chemistry)en
dc.subjectChemistryen
dc.subject.classification1976 Dissertation V226
dc.subject.lcshRadicals (Chemistry)en
dc.subject.lcshElectrolytic oxidationen
dc.titleOxygen based radicals in organic chemistryen
dc.typeThesisen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
dc.contributor.committeeMemberO'Brien, Daniel
dc.type.genredissertationsen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen
dc.publisher.digitalTexas A&M University. Libraries
dc.identifier.oclc2490973


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