What is optical isomerism in tartaric acid?
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Optical Activity of Tartaric Acid Stereoisomers. (R,R)-tartaric acid is the naturally occurring form. ... Thus the chirality of the two asymmetric carbon atoms cancels and this molecule is not optically active
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Explanation:
- Optical isomerism is arising in the organic molecules which contains a ‘carbon atom’ attached to a four different ‘atoms or groups’.
- A carbon with four different groups or atoms attached is called a chiral centre.
- If a molecule has a chiral centre in their structure then it forms two mirror images. They are non- super impossible “mirror images” of one other. They are called optical isomers.
- Optical isomers are useful in the rotating of “plane polarised light” in opposite directions. One rotates clock wise direction called L- form and another one rotates anti clock wise direction called D- form.
The optical isomer of tartaric acid is as follows and attached below:
Attachments:
![](https://hi-static.z-dn.net/files/de8/291ec62e637c08b90ca639086f42251c.png)
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