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  2. 1-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopentane

    1-Bromopentane or amyl bromide is a bromoalkane and isomer of bromopentane. It is a colorless liquid. It is a colorless liquid. It is found as a natural product in Fucus vesiculosus .

  3. Bromopentane - Wikipedia

    en.wikipedia.org/wiki/Bromopentane

    1-Bromopentane; 2-Bromopentane [1] (chiral) 3-Bromopentane; There are four isomers of monobromopentane based on 2-methylbutane: 1-Bromo-2-methylbutane (chiral)

  4. 2-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopentane

    2-Bromopentane is a bromoalkane and isomer of bromopentane. It is a colorless liquid. 2-Bromopentane is chiral and thus can be obtained as either of two stereoisomers designated as ( R )-2-bromopentane and ( S )-2-bromopentane, or as a racemic 1:1 mixture of the two enantiomers .

  5. 3-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/3-Bromopentane

    3-Bromopentane is a bromoalkane and isomer of bromopentane. It is a colorless liquid. References This page was last edited on 27 February 2024, at 20:34 (UTC). Text ...

  6. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Tetrafluoroethane (a haloalkane) is a colorless liquid that boils well below room temperature (as seen here) and can be extracted from common canned air canisters by simply inverting them during use.

  7. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    As a primary haloalkane, it is prone to S N 2 type reactions. It is commonly used as an alkylating agent.When combined with magnesium metal in dry ether, it gives the corresponding Grignard reagent.

  8. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    1-Bromopropane (n-propylbromide or nPB) is a bromoalkane with the chemical formula CH 3 CH 2 CH 2 Br. It is a colorless liquid that is used as a solvent. It has a characteristic hydrocarbon odor.

  9. Weinreb ketone synthesis - Wikipedia

    en.wikipedia.org/wiki/Weinreb_ketone_synthesis

    Weinreb and Nahm originally proposed the following reaction mechanism to explain the selectivity shown in reactions of the Weinreb–Nahm amide. Their suggestion was that the tetrahedral intermediate (A below) formed as a result of nucleophilic addition by the organometallic reagent is stabilized by chelation from the methoxy group as shown. [1]