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  2. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    A halogen addition reaction is a simple organic reaction where a halogen molecule is added to the carbon–carbon double bond of an alkene functional group. [1] The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 ...

  3. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus. [citation needed] Chlorine adds to the multiple bonds on alkenes and alkynes as well, giving di- or tetra-chloro compounds. [citation needed]

  4. Photochlorination - Wikipedia

    en.wikipedia.org/wiki/Photochlorination

    Photochlorination is a chlorination reaction that is initiated by light. Usually a C-H bond is converted to a C-Cl bond. Photochlorination is carried out on an industrial scale. The process is exothermic and proceeds as a chain reaction initiated by the homolytic cleavage of molecular chlorine into chlorine radicals by ultraviolet radiation ...

  5. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    Two free radicals (chlorine and chlorine, chlorine and methyl, or methyl and methyl) combine: Methane chlorination: termination The last possibility generates in an impurity in the final mixture (notably, an organic molecule with a longer carbon chain than the reactants). The net reaction is: Methane chlorination overall reaction

  6. Reductive dechlorination - Wikipedia

    en.wikipedia.org/wiki/Reductive_dechlorination

    Usually stoichiometric amounts of dechlorinating agent are required. In one classic application, the Ullmann reaction, chloroarenes are coupled to biphenyl]]s. For example, the activated substrate 2-chloronitrobenzene is converted into 2,2'-dinitrobiphenyl with a copper - bronze alloy. [1] [2] Ullmann reaction. Zerovalent iron effects similar ...

  7. Chlorine oxide - Wikipedia

    en.wikipedia.org/wiki/Chlorine_oxide

    Chlorine and oxygen can bond in a number of ways: chlorine monoxide radical, ClO•, chlorine (II) oxide radical; chloroperoxyl radical, ClOO•, chlorine (II) peroxide radical; chlorine dioxide, ClO 2, chlorine (IV) oxide; chlorine trioxide radical, ClO 3 •, chlorine (VI) oxide radical; chlorine tetroxide radical, ClO 4 •, chlorine (VII ...

  8. Interhalogen - Wikipedia

    en.wikipedia.org/wiki/Interhalogen

    It has the same molecular shape as chlorine trifluoride. Iodine trifluoride (IF 3) is a yellow solid that decomposes above −28 °C. It can be synthesised from the elements, but care must be taken to avoid the formation of IF 5. F 2 attacks I 2 to yield IF 3 at −45 °C in CCl 3 F. Alternatively, at low temperatures, the fluorination reaction

  9. Reed reaction - Wikipedia

    en.wikipedia.org/wiki/Reed_reaction

    The Reed reaction. Polyethylene is treated with a mixture of chlorine and sulfur dioxide under UV-radiation. Vinylsulfonic acid can also be prepared beginning with the sulfochlorination of chloroethane. Dehydrohalogenation of the product gives vinylsulfonyl chloride, which subsequently is hydrolyzed to give vinylsulfonic acid: