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  2. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. ... For example, carboxylates salts are converted to ethyl esters, [6] ...

  3. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    For example, ethane with bromine becomes bromoethane, methane with four chlorine groups becomes tetrachloromethane. However, many of these compounds have already an established trivial name, which is endorsed by the IUPAC nomenclature, for example chloroform (trichloromethane) and methylene chloride (dichloromethane). But nowadays, IUPAC ...

  4. 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.

  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. Ethyl group - Wikipedia

    en.wikipedia.org/wiki/Ethyl_group

    Ethyl group (highlighted blue) as part of a molecule, as the ethyl radical, and in the compounds ethanol, bromoethane, ethyl acetate, and ethyl methyl ether.. In organic chemistry, an ethyl group (abbr. Et) is an alkyl substituent with the formula −CH 2 CH 3, derived from ethane (C 2 H 6).

  7. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    In another route, ethylamine can be synthesized via nucleophilic substitution of a haloethane (such as chloroethane or bromoethane) with ammonia, utilizing a strong base such as potassium hydroxide. This method affords significant amounts of byproducts, including diethylamine and triethylamine. [6] CH 3 CH 2 Cl + NH 3 + KOH → CH 3 CH 2 NH 2 ...

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  9. 1,1-Dibromoethane - Wikipedia

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

    1,1-Dibromoethane is a clear, slightly brown, flammable chemical compound. [3] It is classified as the organobromine compound, and has the chemical formula C 2 H 4 Br 2 [4] and it is a position isomer of 1,2-dibromoethane.