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  2. 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]

  3. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  4. Category:Bromoalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkanes

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  5. File:2-Bromohexane Structural formula V1.svg - Wikipedia

    en.wikipedia.org/wiki/File:2-Bromohexane...

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  6. Chemosynthesis - Wikipedia

    en.wikipedia.org/wiki/Chemosynthesis

    Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...

  7. Dynamic kinetic resolution in asymmetric synthesis - Wikipedia

    en.wikipedia.org/wiki/Dynamic_Kinetic_Resolution...

    About a decade later, Jurkauskas and Buchwald also utilized dynamic kinetic resolution towards the hydrogenation of conjugated systems. [8] 1,4 addition to cyclic enones is quite common in many reaction schemes, however asymmetric reductions in the presence of an easily epimerizable center adds to the complexity when trying to modify only one center.

  8. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    Likewise, 1-chloropropane and 2-chloropropane give propene. Zaitsev's rule helps to predict regioselectivity for this reaction type. In general, the reaction of a haloalkane with potassium hydroxide can compete with an S N 2 nucleophilic substitution reaction by OH − a strong, unhindered nucleophile .

  9. C6H13Br - Wikipedia

    en.wikipedia.org/wiki/C6H13Br

    Printable version; In other projects Wikidata item; Appearance. ... 1-Bromohexane; 2-Bromohexane This page was last edited on 12 November 2022, at 16: ...

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