enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 1-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopentane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-pentene in the case of 1-bromopentane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] It is also formed by the reaction of 1-pentanol with hydrogen bromide.

  3. 1-Bromododecane - Wikipedia

    en.wikipedia.org/wiki/1-bromododecane

    1-Bromododecane is a bromoalkane with the formula Br(CH 2) 11 CH 3. It is a colorless liquid. It is a colorless liquid. It is used as a long chain alkylating agent to improve the lipophilicity and hydrophobicity of organic molecules for biological applications.

  4. Category:Bromoalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkanes

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  5. Category:Bromoalkenes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkenes

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  6. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene. These conditions lead to the anti-Markovnikov addition, i.e. give the 1-bromo derivatives. [2] 1-Bromobutane can also be prepared from butanol by treatment with hydrobromic acid: [3] CH 3 (CH 2) 3 OH + HBr → CH 3 (CH 2) 3 Br + H 2 O

  7. 2-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/2-Bromohexane

    Most 2-bromoalkanes are prepared by addition of hydrogen bromide to the 1-alkene. Markovnikov addition proceeds in the absence of free-radicals, i.e. give the 2-bromo derivatives. [ 2 ]

  8. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    The reaction mechanism for an alkene bromination can be described as follows. In the first step of the reaction, a bromine molecule approaches the electron-rich alkene carbon–carbon double bond. The bromine atom closer to the bond takes on a partial positive charge as its electrons are repelled by the electrons of the double bond.

  9. 1-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/1-Bromohexane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] 1-Bromohexane undergoes reactions expected of simple alkyl bromides. It can form Grignard reagents. [3]