Bromination of Substituted Anilides

dc.contributor.author	Reader, Vera Birdie
dc.date.accessioned	2011-12-13T21:29:47Z
dc.date.accessioned	2022-10-31T22:14:54Z
dc.date.available	2011-12-13T21:29:47Z
dc.date.available	2022-10-31T22:14:54Z
dc.date.copyright	1923
dc.date.issued	1923
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/27195
dc.description.abstract	The rate of bromination of Aromatic compounds has been found to vary greatly, some reactions being almost instantaneous, e.g. bromination of phenol with three molecules of bromine to form symmetrical tribromo-phenol, whilst some are very slow, occasionally months passing before one molecule completely enters. In all cases the rate is greatly increased if a halogen carrier, e.g. iodine (Muller 1862) red phosphorus (Volhard 1885) or hydrogen chloride (Lapworth 1903) etc., is present.	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	Bromination of Substituted Anilides	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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