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

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dc.contributor.author Lees, Alexander Clark
dc.date.accessioned 2011-12-13T21:29:04Z
dc.date.accessioned 2022-10-31T22:02:44Z
dc.date.available 2011-12-13T21:29:04Z
dc.date.available 2022-10-31T22:02:44Z
dc.date.copyright 1942
dc.date.issued 1942
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/27174
dc.description.abstract The 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.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 The bromination of allyl acetate and allyl benzoate in carbon tetrachloride and chloroform en_NZ
dc.type Text en_NZ
vuwschema.type.vuw Awarded Research Masters Thesis en_NZ
thesis.degree.discipline Chemistry en_NZ
thesis.degree.grantor Te Herenga Waka—Victoria University of Wellington en_NZ
thesis.degree.level Masters en_NZ


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