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Was (wer) ist cyanogenic$18354$ - definition
![Removal of cyanide from [[cassava]] in [[Nigeria]].](https://commons.wikimedia.org/wiki/Special:FilePath/Removal of cyanide poison from cassava.jpg?width=200 "Removal of cyanide from [[cassava]] in [[Nigeria]].")
![[[Amygdalin]]](https://commons.wikimedia.org/wiki/Special:FilePath/Amygdalin skeletal.png?width=200 "[[Amygdalin]]")
![Chemical structure of [[oleandrin]], a [[cardiac glycoside]]](https://commons.wikimedia.org/wiki/Special:FilePath/Oleandrin-skeletal.svg?width=200 "Chemical structure of [[oleandrin]], a [[cardiac glycoside]]")
In chemistry, a cyanide (from Greek kyanos 'dark blue') is a chemical compound that contains a C≡N functional group. 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, also known as hydrogen cyanide, or HCN, 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. For example, in acetonitrile (CH3−C≡N), the cyanide group is bonded to methyl (−CH3). Although nitriles generally do not release cyanide ions, the cyanohydrins do and are thus rather toxic.
Wikipedia
In chemistry, a cyanide (from Greek kyanos 'dark blue') is a chemical compound that contains a C≡N functional group. 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 cyanide anion −C≡N. This anion is extremely poisonous. Soluble salts such as sodium cyanide (NaCN) and potassium cyanide (KCN) are highly toxic. Hydrocyanic acid, also known as hydrogen cyanide, or HCN, 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 single covalent bond to carbon. For example, in acetonitrile (CH3−C≡N), the cyanide group is bonded to methyl (−CH3). Although nitriles generally do not release cyanide ions, the cyanohydrins do and are thus rather toxic.
