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  2. Tetrabromoethane - Wikipedia

    en.wikipedia.org/wiki/Tetrabromoethane

    1,1,2,2-Tetrabromoethane, or simply tetrabromoethane (TBE), is a halogenated hydrocarbon, chemical formula C 2 H 2 Br 4.Although three bromine atoms may bind to one of the carbon atoms creating 1,1,1,2-tetrabromoethane this is not thermodynamically favorable, so in practice tetrabromoethane is equal to 1,1,2,2-tetrabromoethane, where each carbon atom binds two bromine atoms.

  3. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  4. Carbon tetrabromide - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrabromide

    Names Preferred IUPAC name. Tetrabromomethane [2] Other names ... Due to its symmetrically substituted tetrahedral structure, its dipole moment is 0 Debye. Critical ...

  5. 1,2-Dibromoethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Dibromoethane

    1,2-Dibromoethane, also known as ethylene dibromide (EDB), is an organobromine compound with the chemical formula C 2 H 4 Br 2.Although trace amounts occur naturally in the ocean, where it is probably formed by algae and kelp, substantial amounts are produced industrially.

  6. 1,2-Dibromoethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dibromoethylene

    1,2-Dibromoethylene can be synthesized by halogenation of acetylene (C 2 H 2) with bromine (Br 2). [1] In order to prevent the formation of tetrahalogenated compounds, acetylene is used in excess, with Br 2 as the limiting reagent.

  7. C2H4Br2 - Wikipedia

    en.wikipedia.org/wiki/C2H4Br2

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  8. Cyanogen bromide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_bromide

    Cyanogen bromide is often used to immobilize proteins by coupling them to reagents such as agarose for affinity chromatography. [5] Because of its simplicity and mild pH conditions, cyanogen bromide activation is the most common method for preparing affinity gels.

  9. 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. One method involves its conversion to the Grignard reagent, phenylmagnesium bromide.