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  2. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane is inexpensive and would rarely be prepared in the laboratory. A laboratory synthesis includes reacting ethanol with a mixture of hydrobromic and sulfuric acids . An alternate route involves refluxing ethanol with phosphorus and bromine ; phosphorus tribromide is generated in situ .

  3. 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.

  4. Chloroethane - Wikipedia

    en.wikipedia.org/wiki/Chloroethane

    Chloroethane is produced by hydrochlorination of ethylene: [11]. C 2 H 4 + HCl → C 2 H 5 Cl. At various times in the past, chloroethane has also been produced from ethanol and hydrochloric acid, from ethane and chlorine, or from ethanol and phosphorus trichloride, but these routes are no longer economical.

  5. 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).

  6. 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.

  7. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    As can be seen, the OH is now attached to the alkyl group, creating an alcohol. (Hydrolysis of bromoethane, for example, yields ethanol). Reactions with ammonia give primary amines. Chloro- and bromoalkanes are readily substituted by iodide in the Finkelstein reaction. The iodoalkanes produced easily undergo further reaction.

  8. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    1-Bromopropane (n-propylbromide or nPB) is a bromoalkane with the chemical formula CH 3 CH 2 CH 2 Br. It is a colorless liquid that is used as a solvent. It has a characteristic hydrocarbon odor.

  9. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH. It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl. Ethanol is a volatile, flammable, colorless liquid with a characteristic wine-like ...