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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.
The cyanide source can be potassium cyanide (KCN), sodium cyanide (NaCN) or trimethylsilyl cyanide ((CH 3) 3 SiCN). With aromatic aldehydes such as benzaldehyde, the benzoin condensation is a competing reaction. The reaction is used in carbohydrate chemistry as a chain extension method for example that of D-xylose.
This reaction is akin to steam reforming, the reaction of methane and water to give carbon monoxide and hydrogen. In the Shawinigan Process, hydrocarbons, e.g. propane, are reacted with ammonia. In the laboratory, small amounts of HCN are produced by the addition of acids to cyanide salts of alkali metals: H + + CN − → HCN
Potassium cyanide is a compound with the formula KCN. It is a colorless salt, similar in appearance to sugar, that is highly soluble in water. Most KCN is used in gold mining, organic synthesis, and electroplating. Smaller applications include jewellery for chemical gilding and buffing. [4]
According to the database at astrochemistry.net, the most advanced chemical models of HCNH + include 71 total formation reactions and 21 total destruction reactions. Of these, however, only a handful dominate the overall formation and destruction. [13] In the case of formation, the 7 dominant reactions are: H + 3 + HCN → HCNH + + H 2 H + 3 ...
Many characteristic reactions of metal cyanides arise from ambidentate nature of cyanide, i.e. both the nitrogen and the carbon extremities of the anion are basic. Thus cyanometalates can be alkylated to give isocyanide complexes. [20] Cyanide ligands are susceptible to protonation, hence many cyanometalates are highly solvatochromic. The ...
Flow injection analysis (FIA) was first described by Ruzicka and Hansen in Denmark in 1974 and Stewart and coworkers in United States in 1979. FIA is a popular, simple, rapid, and versatile technique which is a well-established position in modern analytical chemistry, and widespread application in quantitative chemical analysis.
The reduction of nitro compounds are chemical reactions of wide interest in organic chemistry. The conversion can be effected by many reagents. The nitro group was one of the first functional groups to be reduced. Alkyl and aryl nitro compounds behave differently.