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  2. Lithium aluminium hydride - Wikipedia

    en.wikipedia.org/wiki/Lithium_aluminium_hydride

    Lithium aluminium hydride, commonly abbreviated to LAH, is an inorganic compound with the chemical formula Li[Al H 4] or LiAlH 4.It is a white solid, discovered by Finholt, Bond and Schlesinger in 1947. [4]

  3. Lithium borohydride - Wikipedia

    en.wikipedia.org/wiki/Lithium_borohydride

    Lithium borohydride reacts with water to produce hydrogen. This reaction can be used for hydrogen generation. [8] Although this reaction is usually spontaneous and violent, somewhat-stable aqueous solutions of lithium borohydride can be prepared at low temperature if degassed, distilled water is used and exposure to oxygen is carefully avoided. [9]

  4. Amine alkylation - Wikipedia

    en.wikipedia.org/wiki/Amine_alkylation

    Amine alkylation (amino-dehalogenation) is a type of organic reaction between an alkyl halide and ammonia or an amine. [1] The reaction is called nucleophilic aliphatic substitution (of the halide), and the reaction product is a higher substituted amine. The method is widely used in the laboratory, but less so industrially, where alcohols are ...

  5. McMurry reaction - Wikipedia

    en.wikipedia.org/wiki/McMurry_reaction

    The reaction is named after its co-discoverer, John E. McMurry. The McMurry reaction originally involved the use of a mixture TiCl 3 and LiAlH 4 , which produces the active reagents. Related species have been developed involving the combination of TiCl 3 or TiCl 4 with various other reducing agents, including potassium , zinc , and magnesium .

  6. Amide reduction - Wikipedia

    en.wikipedia.org/wiki/Amide_reduction

    Amide reduction is a reaction in organic synthesis where an amide is reduced to either an amine or an aldehyde functional group. [1] [2] Catalytic hydrogenation

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  8. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

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