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  2. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    In organic chemistry, a cyanohydrin reaction is an organic reaction in which an aldehyde (−CH=O) or ketone (>C=O) reacts with a cyanide anion ...

  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. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Well-known reactions and reagents in organic chemistry include ... Cyanohydrin reaction; D ... Swain equation; Swarts reaction; Swern oxidation; T

  5. Kiliani–Fischer synthesis - Wikipedia

    en.wikipedia.org/wiki/Kiliani–Fischer_synthesis

    The Kiliani–Fischer synthesis, named for German chemists Heinrich Kiliani and Emil Fischer, is a method for synthesizing monosaccharides.It proceeds via synthesis and hydrolysis of a cyanohydrin, followed by reduction of the intermediate acid to the aldehyde, thus elongating the carbon chain of an aldose by one carbon atom while preserving stereochemistry on all the previously present chiral ...

  6. Cyanation - Wikipedia

    en.wikipedia.org/wiki/Cyanation

    Cyanation of ketones or aldehydes yields the corresponding cyanohydrins, which can be done directly with the cyanide ion (the cyanohydrin reaction) or by using bisulfite, followed by displacement of sulfite: [3] [4] Cyanation of aldehyde with bisulfite. A related reaction is hydrocyanation, which installs the elements of H-CN.

  7. Strecker amino acid synthesis - Wikipedia

    en.wikipedia.org/wiki/Strecker_amino_acid_synthesis

    The German chemist Adolph Strecker discovered the series of chemical reactions that produce an amino acid from an aldehyde or ketone. [9] [10] Using ammonia or ammonium salts in this reaction gives unsubstituted amino acids. In the original Strecker reaction acetaldehyde, ammonia, and hydrogen cyanide combined to form after hydrolysis alanine ...

  8. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    Cyanide is unstable in water, but the reaction is slow until about 170 °C. It undergoes hydrolysis to give ammonia and formate, which are far less toxic than cyanide: [14] CN − + 2 H 2 O → HCO − 2 + NH 3. Cyanide hydrolase is an enzyme that catalyzes this reaction.

  9. Glycolonitrile - Wikipedia

    en.wikipedia.org/wiki/Glycolonitrile

    Glycolonitrile, also called hydroxyacetonitrile or formaldehyde cyanohydrin, is the organic compound with the formula HOCH 2 CN. It is the simplest cyanohydrin and it is derived from formaldehyde. [3] It is a colourless liquid that dissolves in water and ether.