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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. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Illustrative of the bromination of an alkene is the route to the anesthetic halothane from trichloroethylene: [6] Iodination and bromination can be effected by the addition of iodine and bromine to alkenes. The reaction, which conveniently proceeds with the discharge of the color of I 2 and Br 2, is the basis of the analytical method.

  4. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    [3]: 188, 751 The result is typically anti-Markovnikov addition, a phenomenon Morris Kharasch called the "peroxide effect". [4] Reaction is slower with alkynes than alkenes. [3]: 750 In the paradigmatic example, hydrogen bromide radicalyzes to monatomic bromine. These bromine atoms add to an alkene at the most accessible site, to give a ...

  5. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger one than iodine. This can be seen from the standard electrode potentials of the X 2 /X − couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V ...

  6. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    The reaction mechanism for chlorination of benzene is the same as bromination of benzene. Iron(III) bromide and iron(III) chloride become inactivated if they react with water, including moisture in the air. Therefore, they are generated by adding iron filings to bromine or chlorine. Here is the mechanism of this reaction:

  7. Halonium ion - Wikipedia

    en.wikipedia.org/wiki/Halonium_ion

    Many halonium ions have a three-atom cyclic structure, similar to that of an epoxide, resulting from the formal addition of a halogenium ion X + to a C=C double bond, as when a halogen is added to an alkene. [1] The formation of 5-membered halonium ions (e.g., chlorolanium, bromolanium ions) via neighboring group participation is also well ...

  8. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  9. Kharasch addition - Wikipedia

    en.wikipedia.org/wiki/Kharasch_addition

    chemical reactions for the Kharasch addition reaction of chloroform to a terminal alkene. The Kharasch addition is an organic reaction and a metal-catalysed free radical addition of CXCl 3 compounds (X = Cl, Br, H) to alkenes. [1] The reaction is used to append trichloromethyl or dichloromethyl groups to terminal alkenes.