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The Addition of bromine to phenylpropiolic acid

dc.contributor.authorFreeman, Douglas Haig
dc.date.accessioned2010-11-17T20:04:57Z
dc.date.accessioned2022-10-10T20:25:59Z
dc.date.available2010-11-17T20:04:57Z
dc.date.available2022-10-10T20:25:59Z
dc.date.copyright1941
dc.date.issued1941
dc.description.abstractConsiderable attention has recently been focused upon the nature of the kinetics of halogen additions to unsaturated compounds Probably the first noteworthy contribution towards the establishment of the mechanics of additions to ethylenic compounds was set forth by Lowry (1), when he gave an explanation of the electron distribution and consequent polarity associated with the unsaturated ethylenic system, which was followed by a further suggestion by Francis (2), relating to bromine addition in aqueous solution. Later, the examination of halogen addition to the double bondwas made by Ingold and Ingold (3) in terms of electronic theory, and the present theory based upon their investigation has since had substantial confirmation.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/21585
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.subjectChemical reactionsen_NZ
dc.subjectBrominationen_NZ
dc.titleThe Addition of bromine to phenylpropiolic aciden_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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