Cyanide: Difference between revisions
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Organic cyanides are usually called nitriles. In nitriles, the C≡N group is linked by a covalent bond to carbon. Although nitriles generally do not release cyanide ions, the cyanohydrins do and are thus rather toxic. | Organic cyanides are usually called nitriles. In nitriles, the C≡N group is linked by a covalent bond to carbon. Although nitriles generally do not release cyanide ions, the cyanohydrins do and are thus rather toxic. | ||
== Dependencies == | |||
* [[Carbon]] | |||
* [[Nitrogen]] | |||
** '''Cyanide''' | |||
== See also == | == See also == | ||
* [[Hydrogen]] | |||
* [[Potassium]] | |||
* [[Sodium]] | |||
* [[Chemical compounds]] | * [[Chemical compounds]] | ||
Revision as of 14:44, 21 November 2022
Cyanide are chemical compounds that contains a C≡N functional group (a substituent which causes the molecule's characteristic chemical reactions). This group, known as the cyano group, consists of a carbon atom triple-bonded to a nitrogen atom.
In inorganic cyanides, the cyanide group is present as the anion −C≡N. Soluble salts such as sodium cyanide (NaCN) and potassium cyanide (KCN) are highly toxic. Hydrocyanic acid (HCN), also known as hydrogen cyanide, is a highly volatile liquid that is produced on a large scale industrially. It is obtained by acidification of cyanide salts.
Organic cyanides are usually called nitriles. In nitriles, the C≡N group is linked by a covalent bond to carbon. Although nitriles generally do not release cyanide ions, the cyanohydrins do and are thus rather toxic.
Dependencies
See also
References
| This article uses material from the Wikipedia article Cyanide, which is released under the Creative Commons Attribution-ShareAlike 3.0 Unported License (view authors). | 
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