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  2. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    RCH=CH 2 + HBr → RCHBrCH 3. Under free radical conditions, the direction of the addition can be reversed. Free-radical addition is used commercially for the synthesis of 1-bromoalkanes, precursors to tertiary amines and quaternary ammonium salts. 2-Phenethyl bromide (C 6 H 5 CH 2 CH 2 Br) is produced via this route from styrene.

  3. 2-Phenylethyl bromide - Wikipedia

    en.wikipedia.org/wiki/2-Phenylethyl_bromide

    2-Phenylethyl bromide is an organobromide with the formula C 6 H 5 CH 2 CH 2 Br. It is a colorless liquid, although older samples appear yellow. Analogous to the preparation of most 1-bromoalkanes, it is prepared by free-radical addition of hydrogen bromide to styrene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo ...

  4. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    In the CF 3 radical the fluorine atom is an electron-withdrawing group via the inductive effect but also a weak pi donor through interaction of the fluorine lone pair with the radical center's SOMO. Compared to the methyl radical the CF 3 radical is pyramidal (angle 107.8 °C ) with a large inversion barrier, electrophilic and also more

  5. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    Bromomethane, commonly known as methyl bromide, is an organobromine compound with formula C H 3 Br. This colorless, odorless, nonflammable gas is produced both industrially and biologically. This colorless, odorless, nonflammable gas is produced both industrially and biologically.

  6. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It is a colourless liquid with a pleasant floral odor.

  7. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

  8. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Three of these alcohols, 2-methyl-1-butanol, 2-pentanol, and 3-methyl-2-butanol (methyl isopropyl carbinol), contain stereocenters, and are therefore chiral and optically active. The most important amyl alcohol is isoamyl alcohol , the chief one generated by fermentation in the production of alcoholic beverages and a constituent of fusel oil .

  9. Methyltriphenylphosphonium bromide - Wikipedia

    en.wikipedia.org/wiki/Methyltriphenylphosphonium...

    Methyltriphenylphosphonium bromide is produced by treating triphenylphosphine with methyl bromide: [1] Ph 3 P + CH 3 Br → Ph 3 PCH 3 Br. Methyltriphenylphosphonium bromide is the principal precursor to methylenetriphenylphosphorane, a useful methylenating reagent. This conversion is achieved by treating methyltriphenylphosphonium bromide with ...