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  2. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Haloalkanes can also be classified according to the type of halogen on group 17 responding to a specific halogenoalkane. Haloalkanes containing carbon bonded to fluorine, chlorine, bromine, and iodine results in organofluorine, organochlorine, organobromine and organoiodine compounds, respectively.

  3. Halocarbon - Wikipedia

    en.wikipedia.org/wiki/Halocarbon

    Halocarbon. Halocarbon compounds are chemical compounds in which one or more carbon atoms are linked by covalent bonds with one or more halogen atoms (fluorine, chlorine, bromine or iodine – group 17) resulting in the formation of organofluorine compounds, organochlorine compounds, organobromine compounds, and organoiodine compounds.

  4. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    List of straight-chain alkanes. The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [1][2] Number of C atoms. Number of isomers [3][4] Number of isomers including stereoisomers [3][5] Molecular Formula. Name of straight chain.

  5. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. It is abbreviated by chemists as EtBr (which is also used as an abbreviation for ethidium bromide). This volatile compound has an ether-like odor.

  6. 1,1,1,2-Tetrafluoroethane - Wikipedia

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

    1,1,1,2-Tetrafluoroethane is a non-flammable gas used primarily as a "high-temperature" refrigerant for domestic refrigeration and automobile air conditioners. These devices began using 1,1,1,2-tetrafluoroethane in the early 1990s as a replacement for the more environmentally harmful R-12. Retrofit kits are available to convert units that were ...

  7. Halomethane - Wikipedia

    en.wikipedia.org/wiki/Halomethane

    Haloalkanes are diverse in their properties, making generalizations difficult. Few are acutely toxic, but many pose risks from prolonged exposure. Some problematic aspects include carcinogenicity and liver damage (e.g., carbon tetrachloride). Under certain combustion conditions, chloromethanes convert to phosgene, which is highly toxic.

  8. Haloalkane dehalogenase - Wikipedia

    en.wikipedia.org/wiki/Haloalkane_dehalogenase

    In enzymology, a haloalkane dehalogenase (EC 3.8.1.5) is an enzyme that catalyzes the chemical reaction 1-haloalkane + H 2 O ⇌ {\displaystyle \rightleftharpoons } a primary alcohol + halide Thus, the two substrates of this enzyme are 1-haloalkane and H 2 O, whereas its two products are primary alcohol and halide. This enzyme belongs to the family of hydrolases, specifically those acting on ...

  9. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    Hydrohalogenation. A hydrohalogenation reaction is the electrophilic addition of hydrogen halides like hydrogen chloride or hydrogen bromide to alkenes to yield the corresponding haloalkanes. [1][2][3] If the two carbon atoms at the double bond are linked to a different number of hydrogen atoms, the halogen is found preferentially at the carbon ...