An investigation of the nature of p-azophenol

dc.contributor.author	Chamberlain, Edward Edinborough
dc.date.accessioned	2011-12-13T21:26:50Z
dc.date.accessioned	2022-10-31T21:24:05Z
dc.date.available	2011-12-13T21:26:50Z
dc.date.available	2022-10-31T21:24:05Z
dc.date.copyright	1928
dc.date.issued	1928
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/27089
dc.description.abstract	The 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.format	pdf	en_NZ
dc.language	en_NZ
dc.language.iso	en_NZ
dc.publisher	Te Herenga Waka—Victoria University of Wellington	en_NZ
dc.title	An investigation of the nature of p-azophenol	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ

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