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Halogen substitution in aromatic compounds

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dc.contributor.author Swindale, Leslie Denis
dc.date.accessioned 2011-03-10T22:51:55Z
dc.date.accessioned 2022-10-25T04:29:57Z
dc.date.available 2011-03-10T22:51:55Z
dc.date.available 2022-10-25T04:29:57Z
dc.date.copyright 1950
dc.date.issued 1950
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/23161
dc.description.abstract It is a feature of the chemistry of aromatic compounds that halogens substitute in the ring much more easily than they add. In fact substituent groups have similar effects in aromatic substitution as they have in addition to unsaturated compounds. We find that we can postulate similar mechanisms for both types. Let us them examine the principles which govern these mechanisms:- (1) Condition of the Halogen. Firstly it appears positively established that halogenation represents an electrophilic mode of attack. There is much experimental evidence in support of this, including:- (a) Bromine substitution is accelerated by electron repelling groups in the molecule and retarded by electron attracting groups. 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 substitution in aromatic compounds 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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