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An investigation of the nature of p-azophenol

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dc.contributor.authorChamberlain, Edward Edinborough
dc.date.accessioned2011-12-13T21:26:50Z
dc.date.accessioned2022-10-31T21:24:05Z
dc.date.available2011-12-13T21:26:50Z
dc.date.available2022-10-31T21:24:05Z
dc.date.copyright1928
dc.date.issued1928
dc.description.abstractThe isomerism of p-azophenol was first studied in detail by R. Willstätter and M. Benz (Ber. 1906, 39, 3492; 1907, 40, 1578). They found that azophenol obtained directly by the alkali fusion of p-nitrophenol differed from that obtained by the reduction of benzoquinoneazine, which is itself the oxidation product of p-azophenol. The object of their work was to discover the nature of this isomerism. A careful survey of their results led them to classify these isomers as geometric isomers.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/27089
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.rights.holderAll rights, except those explicitly waived, are held by the Authoren_NZ
dc.rights.licenseAuthor Retains Copyrighten_NZ
dc.rights.urihttps://www.wgtn.ac.nz/library/about-us/policies-and-strategies/copyright-for-the-researcharchive
dc.subjectAzo compoundsen_NZ
dc.subjectChemistryen_NZ
dc.titleAn investigation of the nature of p-azophenolen_NZ
dc.typeTexten_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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