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.

May 20, 2025 · Acetone cyanohydrin - cas 75-86-5, synthesis, structure, density, melting point, boiling point

In order to form a cyanohydrin, a hydrogen cyanide adds reversibly to the carbonyl group of an organic compound thus forming a hydroxyalkanenitrile adducts (commonly known and called …

The addition of cyanide ion to the carbonyl group is another common reaction of aldehydes and ketones. The product of these reactions is a cyanohydrin. It works in a slightly basic conditions …

Cyanohydrin is defined as a compound formed by the addition of cyanide to a carbonyl compound, which serves as a versatile synthetic intermediate for the production of various …

An individual cyanohydrin can systematically be named as a hydroxy nitrile, e.g. (CH A 3) A 2 C (OH) C ≡ N 'acetone cyanohydrin' (2-hydroxy-2-methylpropanenitrile), HOCH A 2 CH A 2 C ≡ …

May 23, 2010 · Cyanohydrin From Wikipedia, the free encyclopedia A cyanohydrin is a functional group found in organic compounds. Cyanohydrins have the formula R2C(OH)CN, where R is …

A cyanohydrin is an organic cyanide compound with the general structure R1R2C (OH) (CN), where the hydroxide group and the cyanide group are attached to the same carbon atom.

Cyanohydrin formation, also known as nucleophilic addition of HCN, is a perfect example of base-catalyzed addition of HCN to a carbonyl group. Hydrocyanic acid, HCN, is water soluble and …

Cyanohydrin functional groups often prove useful because of the further chemistry that can be carried out due to the presence of a hydroxyl and a nitrile functionality.