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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. Free base - Wikipedia

    en.wikipedia.org/wiki/Free_base

    Free base (freebase, free-base) is a descriptor for the neutral form of an amine commonly used in reference to illicit drugs. The amine is often an alkaloid , such as nicotine , cocaine , morphine , and ephedrine , or derivatives thereof.

  4. 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.

  5. Bromohexane - Wikipedia

    en.wikipedia.org/?title=Bromohexane&redirect=no

    From Wikipedia, the free encyclopedia. Redirect page

  6. 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 .

  7. 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

  8. 1-Fluorohexane - Wikipedia

    en.wikipedia.org/wiki/1-Fluorohexane

    1-Fluorohexane is a chemical compound from the group of aliphatic saturated halogenated hydrocarbons. [1] The chemical formula is CH 3 (CH 2 ) 5 F . [ 2 ] [ 3 ]

  9. 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 ...