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  2. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Only haloalkanes that contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide , a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated ...

  3. Swarts fluorination - Wikipedia

    en.wikipedia.org/wiki/Swarts_fluorination

    Swarts fluorination is a process whereby the chlorine atoms in a compound – generally an organic compound, but experiments have been performed using silanes – are replaced with fluorine, by treatment with antimony trifluoride in the presence of chlorine or of antimony pentachloride. Some metal fluorides are particularly more useful than ...

  4. Chlorocyclopropane - Wikipedia

    en.wikipedia.org/wiki/Chlorocyclopropane

    The compound is a member of haloalkane family. [2] Synthesis. The compound can be obtained by photoreaction of cyclopropane and chlorine gas; ...

  5. Halocarbon - Wikipedia

    en.wikipedia.org/wiki/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.

  6. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    The relative rates at which different halogens react vary considerably: [citation needed] fluorine (108) > chlorine (1) > bromine (7 × 10 −11) > iodine (2 × 10 −22).. Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction.

  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. Bromochlorodifluoromethane - Wikipedia

    en.wikipedia.org/wiki/Bromochlorodifluoromethane

    Bromochlorodifluoromethane (BCF), also referred to by the code numbers Halon 1211 and Freon 12B1, is a haloalkane with the chemical formula C F 2 Cl Br.It is used for fire suppression, especially for expensive equipment or items that could be damaged by the residue from other types of extinguishers. [1]

  9. Trihalomethane - Wikipedia

    en.wikipedia.org/wiki/Trihalomethane

    Chloroform is produced by heating mixtures of methane or methyl chloride with chlorine. Dichloromethane is a coproduct. [4] Bromochlorofluoromethane is one of the simplest possible stable chiral compounds, and is used for studies.