When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    In primary (1°) haloalkanes, the carbon that carries the halogen atom is only attached to one other alkyl group. An example is chloroethane (CH 3 CH 2 Cl). In secondary (2°) haloalkanes, the carbon that carries the halogen atom has two C–C bonds. In tertiary (3°) haloalkanes, the carbon that carries the halogen atom has three C–C bonds.

  3. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/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 with fewer ...

  4. Category:Haloalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Haloalkanes

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. ... Pages in category "Haloalkanes"

  5. Haloalkanes - Wikipedia

    en.wikipedia.org/?title=Haloalkanes&redirect=no

    Pages for logged out editors learn more. Contributions; Talk; Haloalkanes

  6. α-Halo ketone - Wikipedia

    en.wikipedia.org/wiki/Α-halo_ketone

    The general structure is RR′C(X)C(=O)R where R is an alkyl or aryl residue and X any one of the halogens. The preferred conformation of a halo ketone is that of a cisoid with the halogen and carbonyl sharing the same plane as the steric hindrance with the carbonyl alkyl group is generally larger.

  7. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    In organic chemistry, free-radical halogenation is a type of halogenation. This chemical reaction is typical of alkanes and alkyl -substituted aromatics under application of UV light . The reaction is used for the industrial synthesis of chloroform (CHCl 3 ), dichloromethane (CH 2 Cl 2 ), and hexachlorobutadiene .

  8. 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.

  9. Halon - Wikipedia

    en.wikipedia.org/wiki/Halon

    Haloalkane, or halogenoalkane, a group of chemical compounds consisting of alkanes with linked halogens (in particular, bromine-containing haloalkanes) Halomethane compounds: Halon 10001 (iodomethane) Halon 1001 (bromomethane) Halon 1011 (bromochloromethane, CH 2 BrCl) Halon 104 (carbon tetrachloride) Halon 1103 (tribromofluoromethane)