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Isomers of Bromochlorobenzene Skeletal formula: General Common names o-bromochlorobenzene ortho-bromochlorobenzene m-bromochlorobenzene meta-bromochlorobenzene p-bromochlorobenzene para-bromochlorobenzene Systematic name: 1-bromo-2-chlorobenzene 1-bromo-3-chlorobenzene 1-bromo-4-chlorobenzene Molecular formula: BrC 6 H 4 Cl Molar mass: 191.45 g ...
For example, the methyl group may be oxidized using potassium permanganate to form the corresponding bromobenzoic acid. [5] The methyl group may also be partially oxidized to form bromobenzaldehyde .
4-Fluorobromobenzene is synthesized via bromination of fluorobenzene in the presence of a Lewis acid catalyst such as iron(III) bromide or aluminium tribromide. [2]4-Bromofluorobenzene is regarded by the Toxic Substances Control Act as a high production volume chemical, that is, a chemical that 1 million pounds (about 500 tonnes) per year is either produced in or imported to the United States.
Chemical formula Synonyms CAS number CAgO carbonylsilver: CCl 2 F 2: dichlorodifluoromethane freon-12: 75-71-8 CCl 4: carbon tetrachloride tetrachloromethane: 56-23-5 C(CN) 4: tetracyanomethane: 24331-09-7 CFCl 3: trichlorofluoromethane freon-11: 75-69-4 CFCl 2 CF 2 Cl: chlorotrifluoromethane freon-13: 75-72-9 CHCl 3: chloroform ...
For compounds consisting of one benzene ring with only bromine and hydrogen as substituents, see Category:Bromobenzenes. Pages in category "Bromobenzene derivatives" The following 69 pages are in this category, out of 69 total.
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Bromobenzene is used to introduce a phenyl group into other compounds. One method involves its conversion to the Grignard reagent , phenylmagnesium bromide . This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid . [ 4 ]
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