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Cyanuric chloride is employed as a reagent in organic synthesis for the conversion of alcohols into alkyl chlorides, [8] and carboxylic acids into acyl chlorides: [9]. It is also used as a dehydrating agent, e.g. in the conversion of amides to nitriles, [10] and for the activation of carboxylic acids for reduction to alcohols.
The Strecker amino acid synthesis, also known simply as the Strecker synthesis, is a method for the synthesis of amino acids by the reaction of an aldehyde with cyanide in the presence of ammonia. The condensation reaction yields an α-aminonitrile, which is subsequently hydrolyzed to give the desired amino acid.
Among the most toxic cyanides are hydrogen cyanide (HCN), sodium cyanide (NaCN), potassium cyanide (KCN), and calcium cyanide (Ca(CN) 2). The cyanide anion is an inhibitor of the enzyme cytochrome c oxidase (also known as aa 3), the fourth complex of the electron transport chain found in the inner membrane of the mitochondria of eukaryotic ...
Reaction mechanism for the amine formation from a carboxylic acid via Schmidt reaction. In the reaction mechanism for the Schmidt reaction of ketones , the carbonyl group is activated by protonation for nucleophilic addition by the azide, forming azidohydrin 3 , which loses water in an elimination reaction to diazoiminium 5.
In 1857 Hugo Schiff observed that the reaction between benzoyl chloride with potassium cyanide produced the desired benzonitrile. [3] Work done later by British chemist Edmund A. Letts delved much deeper into the synthesis of nitriles. Attempting first to add cyano-groups to acetic acid, he obtained a mixture of acetamide and carbonyl sulfide ...
Solutions of calcium cyanide can be prepared by treating calcium hydroxide with hydrogen cyanide. Solid calcium cyanide is produced commercially by heating calcium cyanamide with sodium chloride. The reaction is incomplete. The product is only of 50% purity, other components being sodium cyanide, calcium cyanamide, and carbon. Because of the ...
General chemical structure of an acyl chloride. In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl, where R is a side chain. They are reactive derivatives of carboxylic acids (R−C(=O)OH).
Cyanogen bromide is a solid that is prepared by reacting bromine with hydrocyanic acid salts; it has been used as a chemical pesticide against insects and rodents and as a reagent for the study of protein structure. [7] Cyanogen halides have been found to act as electrolytes in liquid solvents, sulfur dioxide, arsenous chloride, and sulfuryl ...