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  2. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    In organic chemistry, a cyanohydrin reaction is an organic ... Mechanism of the cyanohydrin reaction. ... Cyanohydrin reaction of acetone with potassium cyanide ...

  3. Cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin

    The structure of a general cyanohydrin. In organic chemistry, a cyanohydrin or hydroxynitrile is a functional group found in organic compounds in which a cyano and a hydroxy group are attached to the same carbon atom. The general formula is R 2 C(OH)CN, where R is H, alkyl, or aryl.

  4. Acetone cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Acetone_cyanohydrin

    In the laboratory, this compound may be prepared by treating sodium cyanide with acetone, followed by acidification: [3]. Considering the high toxicity of acetone cyanohydrin, a lab scale production has been developed using a microreactor-scale flow chemistry [4] to avoid needing to manufacture and store large quantities of the reagent.

  5. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    In transhydrocyanation, an equivalent of HCN is transferred from a cyanohydrin, e.g. acetone cyanohydrin, to another HCN acceptor. The transfer is an equilibrium process, initiated by base. The reaction can be driven by trapping reactions or by the use of a superior HCN acceptor, such as an aldehyde. [6]

  6. Hydantoin - Wikipedia

    en.wikipedia.org/wiki/Hydantoin

    The method is very similar to the modern route using alkyl and arylcyanates. The 5,5-dimethyl compound can also be obtained from acetone cyanohydrin (also discovered by Urech: see cyanohydrin reaction) and ammonium carbonate. [3] This reaction type is called the Bucherer–Bergs reaction. [4] [5]

  7. Hydroxynitrilase - Wikipedia

    en.wikipedia.org/wiki/Hydroxynitrilase

    Hence, this enzyme has one substrate, acetone cyanohydrin, and two products, cyanide and acetone. This enzyme belongs to the family of lyases, specifically the aldehyde-lyases, which cleave carbon-carbon bonds. The systematic name of this enzyme class is acetone-cyanohydrin acetone-lyase (cyanide-forming).

  8. Carbohydrate acetalisation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_acetalisation

    In carbohydrate chemistry carbohydrate acetalisation is an organic reaction and a very effective means of providing a protecting group. The example below depicts the acetalisation reaction of D-ribose 1. With acetone or 2,2-dimethoxypropane as the acetalisation reagent the reaction is under thermodynamic reaction control and results in the ...

  9. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile, often abbreviated MeCN (methyl cyanide), is the chemical compound with the formula CH 3 CN and structure H 3 C−C≡N. This colourless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not classed as organic). It is produced mainly as a byproduct of acrylonitrile manufacture.