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The substitution of iodine chloride in certain aromatic compounds

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dc.contributor.authorMartin, Gordon Calder
dc.date.accessioned2010-11-22T23:18:36Z
dc.date.accessioned2022-10-24T23:54:41Z
dc.date.available2010-11-22T23:18:36Z
dc.date.available2022-10-24T23:54:41Z
dc.date.copyright1940
dc.date.issued1940
dc.description.abstractIn this work the mechanism by which IC1 substitutes in various aromatic compounds is studied. That part which treats in detail the mechanism by which IC1 substitutes deals with;- I Acetanilide. II Mesitylene. That part which is treated in less detail consists of a comparison of;- I The rate of substitution of p-acetotoluidide with that of acetanilide. II The rate of substitution of toluene with that of mesitylene. III The rates of substitution of para and ortho chloranilines. As the addition of halogens, and interhalogens, to ethylenic compounds has been studied in detail and has a bearing on the work in hand, a short summary of such additions will be given.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/22604
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.subjectIodineen_NZ
dc.subjectChemistryen_NZ
dc.titleThe substitution of iodine chloride in certain aromatic compoundsen_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

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