enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    The U.S. Clean Air Act (CAA; 42 U.S.C. 7401 et seq.). A 1998 amendment (P.L. 105-178, Title VI) conformed the Clean Air Act phase out date with that of the Montreal Protocol. [17] [18] [10] While the Montreal Protocol severely restricted the use of bromomethane internationally, the United States has successfully lobbied for critical-use ...

  4. Rothemund reaction - Wikipedia

    en.wikipedia.org/wiki/Rothemund_reaction

    A simplified version of Rothemund porphyrin synthesis was described by Alan D. Adler and Frederick R. Longo in 1966. It utilizes mild organic acids as catalysts and reaction medium and is conducted in open air. Seventy aldehydes gave corresponding meso-substituted porphyrins.

  5. Hexabromoethane - Wikipedia

    en.wikipedia.org/wiki/Hexabromoethane

    This article about chemical compounds is a stub. You can help Wikipedia by expanding it.

  6. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  7. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    Short-chain alkyl halides are often carcinogenic.. The bromine atom is at the secondary position, which allows the molecule to undergo dehydrohalogenation easily to give propene, which escapes as a gas and can rupture closed reaction vessels.

  8. Gomberg–Bachmann reaction - Wikipedia

    en.wikipedia.org/wiki/Gomberg–Bachmann_reaction

    The Gomberg–Bachmann reaction, named for the Russian-American chemist Moses Gomberg and the American chemist Werner Emmanuel Bachmann, is an aryl-aryl coupling reaction via a diazonium salt.

  9. 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.