Chiral carbon: Difference between revisions
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A chiral [[Carbon|carbon]] is a carbon [[Atom|atom]] which has 4 different groups attached. For each chiral carbon in a molecule there are 2 optical [[Isomer|isomers]]. This increases exponentially with more chiral carbons, so a molecule with 2 chiral centers would have 4 optical isomers, and a molecule with 3 would have 8 optical isomers. This can be calcultated by 2<sup>n</sup> where n is the number of chiral carbons. In nature often only one optical isomer is produced, for example only [[L-isomer]] amino acids are produced in translation. The difference between L isomers and [[ | A chiral [[Carbon|carbon]], (also known as an asymmetric carbon) is a carbon [[Atom|atom]] which has 4 different groups attached. For each chiral carbon in a molecule there are 2 optical [[Isomer|isomers]]. This increases exponentially with more chiral carbons, so a molecule with 2 chiral centers would have 4 optical isomers, and a molecule with 3 would have 8 optical isomers. This can be calcultated by 2<sup>n</sup> where n is the number of chiral carbons. In nature often only one optical isomer is produced, for example only [[L-isomer]] amino acids are produced in translation. | ||
The difference between L isomers and [[D isomer]] is the direction that they rotate plane polarised light. L isomers rotate light anti-clockwise and D isomers rotate clockwise. A mixture containing equal parts of both enantiomers is call a racemic mixture and has no net rotation on plane polarised light. | |||
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Revision as of 17:56, 4 December 2015
A chiral carbon, (also known as an asymmetric carbon) is a carbon atom which has 4 different groups attached. For each chiral carbon in a molecule there are 2 optical isomers. This increases exponentially with more chiral carbons, so a molecule with 2 chiral centers would have 4 optical isomers, and a molecule with 3 would have 8 optical isomers. This can be calcultated by 2n where n is the number of chiral carbons. In nature often only one optical isomer is produced, for example only L-isomer amino acids are produced in translation.
The difference between L isomers and D isomer is the direction that they rotate plane polarised light. L isomers rotate light anti-clockwise and D isomers rotate clockwise. A mixture containing equal parts of both enantiomers is call a racemic mixture and has no net rotation on plane polarised light.