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Alkaline hydrolysis of substituted anilides

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dc.contributor.author O'Connor, Myles
dc.date.accessioned 2011-12-13T21:27:44Z
dc.date.accessioned 2022-10-31T21:39:55Z
dc.date.available 2011-12-13T21:27:44Z
dc.date.available 2022-10-31T21:39:55Z
dc.date.copyright 1935
dc.date.issued 1935
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/27124
dc.description.abstract Although considerable work has been done on alkaline hydrolysis in general, the anilides have received comparatively little attention. The object of this Thesis is therefore to determine as far as possible what factors influence the rate of this hydrolysis. As the reaction concerned is included under the heading of acid-base catalysis, it is advisable to consider how the present conception of that theory was arrived at. Following on the work of Ostwald and Arhennuis researches carried out by Dawson, Lenter, Lapworth, Acree, Goldsmidt and others led to the postulation of the "Dual Theory" of Catalysis, in which undissociated molecules of acids and bases, in addition to hydrogen and hydroxl ions were recognised as exerting effect. 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 Alkaline hydrolysis of substituted anilides 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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