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  2. Bromochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/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

  3. Kumada coupling - Wikipedia

    en.wikipedia.org/wiki/Kumada_coupling

    Grignard reagents do not typically couple with chlorinated arenes. This low reactivity is the basis for chemoselectivity for nickel insertion into the C–Br bond of bromochlorobenzene using a NiCl 2-based catalyst. [21] NiCl 2 catalyzed Kumada coupling shows haloselectivity on bromochlorobenzene.

  4. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as aluminium chloride or ferric bromide. [3]Bromobenzene is used to introduce a phenyl group into other compounds.

  5. 1-Bromo-4-fluorobenzene - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-4-fluorobenzene

    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.

  6. Category:Bromobenzene derivatives - Wikipedia

    en.wikipedia.org/wiki/Category:Bromobenzene...

    This page was last edited on 1 February 2024, at 18:48 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. Category:List-Class chemicals articles - Wikipedia

    en.wikipedia.org/wiki/Category:List-Class...

    A. Talk:Acetaldehyde (data page) Talk:Acetic acid (data page) Talk:Acetone (data page) Talk:Acetonitrile (data page) Talk:Acetylmorphine; Talk:Acid anhydride

  8. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Monobromotoluene isomers [1] [2] [3]; Common name Structure Systematic name: 1-bromo-2-methylbenzene 1-bromo-3-methylbenzene 1-bromo-4-methylbenzene Molecular formula

  9. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is used in organic synthesis for the introduction of the benzyl groups when the less expensive benzyl chloride is insufficiently reactive. [6] [7] Benzylations are often achieved in the presence of catalytic amounts of sodium iodide, which generates the more reactive benzyl iodide in situ. [3]