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  2. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    184.5 °c (364.1 °f; 457.7 k) Benzyl bromide is an isomer, which has a bromine substituted for one of the hydrogens of toluene 's methyl group, and it is sometimes named α-bromotoluene. Preparation

  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. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  5. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as aluminium chloride or ferric bromide. [3]Bromobenzene is used to introduce a phenyl group into other compounds.

  6. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is an organic compound with the formula C 6 H 5 CH 2 Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties. The compound is a reagent for introducing benzyl groups. [3] [4]

  7. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    In organic synthesis, EtBr is the synthetic equivalent of the ethyl carbocation (Et +) synthon. [5] In reality, such a cation is not actually formed. For example, carboxylates salts are converted to ethyl esters , [ 6 ] carbanions to ethylated derivatives, thiourea into ethylisothiouronium salts, [ 7 ] and amines into ethylamines.

  8. trans-Propenylbenzene - Wikipedia

    en.wikipedia.org/wiki/Trans-Propenylbenzene

    trans-Propenylbenzene is an organic compound with the formula C 6 H 5 CH=CHCH 3. It is the more stable [ 2 ] of the two isomers of 1-propenylbenzene. Both isomers are colorless flammable liquids.

  9. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    Replacing 1-bromopropane with water or acetone-based adhesives is the preferred NIOSH option for controlling occupational exposure, but other options include engineering controls like isolation and ventilation, administrative controls, and PPE that includes respiratory and skin protection.