Halogen addition to unsaturated hydrocarbons

dc.contributor.author	Heyes, John Kenneth
dc.date.accessioned	2011-12-13T21:28:27Z
dc.date.accessioned	2022-10-31T21:53:18Z
dc.date.available	2011-12-13T21:28:27Z
dc.date.available	2022-10-31T21:53:18Z
dc.date.copyright	1928
dc.date.issued	1928
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/27154
dc.description.abstract	The classical picture of halogen addition to olefins postulated a simultaneous addition of both atoms in the halogen molecule. This view was disproved by McKenzie (Proc. Chem. Soc. 1911, 150) and Frankland (J.C.S. 1912, 673) who showed that trans addition occurred in these reactions. For example, maleic acid gave racemic dibromo succinic acid with bromine, not the meso acid. Norrish (J.C.S. 1923, 3006) found that the reaction ethylene + bromine in the gas phase takes place on a polar surface only, indicating ionic intermediates.	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	Halogen addition to unsaturated hydrocarbons	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ

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