Repository logo
 

Alkaline hydrolysis of substituted anilides

dc.contributor.authorO'Connor, Myles
dc.date.accessioned2011-12-13T21:27:44Z
dc.date.accessioned2022-10-31T21:39:55Z
dc.date.available2011-12-13T21:27:44Z
dc.date.available2022-10-31T21:39:55Z
dc.date.copyright1935
dc.date.issued1935
dc.description.abstractAlthough 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.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/27124
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.subjectHydrolysisen_NZ
dc.subjectChemistryen_NZ
dc.titleAlkaline hydrolysis of substituted anilidesen_NZ
dc.typeTexten_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
thesis.pdf
Size:
6.21 MB
Format:
Adobe Portable Document Format

Collections