enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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

    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 bromoalkyl radical, with the radical on the more substituted carbon.

  5. 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 ...

  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. Electrophile - Wikipedia

    en.wikipedia.org/wiki/Electrophile

    The electrophilic Br-Br molecule interacts with electron-rich alkene molecule to form a π-complex 1. Forming of a three-membered bromonium ion The alkene is working as an electron donor and bromine as an electrophile. The three-membered bromonium ion 2 consisted of two carbon atoms and a bromine atom forms with a release of Br −.

  8. Bill Belichick reportedly wants to return to coaching in 2025 ...

    www.aol.com/sports/bill-belichick-reportedly...

    Bill Belichick has spent a lot of time talking into a microphone about football this season, but he has his sights set higher for next year. According to The Athletic, Belichick wants to return to ...

  9. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Bromine addition to alkene reaction mechanism. An old qualitative test for the presence of the alkene functional group is that alkenes turn brown aqueous bromine solutions colourless, forming a bromohydrin with some of the dibromoalkane also produced. The reaction passes through a short-lived strongly electrophilic bromonium intermediate.