According to the two-stage mechanism of electrophilic aromatic substitution, the halogenation by molecular chlorine and bromine can be formulated by equations ( 1) and ( 2), respectively\*.
Catalysis by HBr in the bromination of o-xylene in acetic acid
β Scribed by E. P. Yesodharan; J. Rajaram; J. C. Kuriacose
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 273 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Abstract
Hydrogen bromide is known to inhibit the bromination of aromatic substrates (ArH), either by fixing up bromine as HBr~3~ or ArH as ArH Β· HBr. However, there is catalysis by HBr in the bromination of mesitylene in acetic acid. The bromination of oβxylene in acetic acid in the dark is found to be autocatalytic, and the reaction is overall third order, first order in oβxylene with the orders in Br~2~ and HBr depending on the concentrations. A composite rate expression involving Br~2~ and HBr as electrophiles has been proposed and verified using iodine bromide as a catalyst where the orders are one in each of the reactants, irrespective of the concentrations used.
π SIMILAR VOLUMES