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The bromination of allyl acetate and allyl benzoate in carbon tetrachloride and chloroform

dc.contributor.authorLees, Alexander Clark
dc.date.accessioned2011-12-13T21:29:04Z
dc.date.accessioned2022-10-31T22:02:44Z
dc.date.available2011-12-13T21:29:04Z
dc.date.available2022-10-31T22:02:44Z
dc.date.copyright1942
dc.date.issued1942
dc.description.abstractThe mechanism of the addition of halogens to the ethylene link has been investigated by various workers. Bromine addition in dissociating solvents involves attack by the positively polarised bromine atom on the negative carbon atom in the ethylenic system. (Robertson, Clare, McNaught and Paul 1.) The resulting positive charge on the other carbon atom is then neutralised by the negative bromine ion. The same authors have shown that bromine adds on by a termolecular mechanism. Chlorine on the other hand adds on by a bimolecular mechanism. (White and Robertson, 2.)en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/27174
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.subjectBromination
dc.subjectallyl acetate
dc.subjectallyl benzoate
dc.subjectcarbon tetrachloride
dc.titleThe bromination of allyl acetate and allyl benzoate in carbon tetrachloride and chloroformen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineChemistryen_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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