On bromination,propionic acid yields two isom | vedclass

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(B) The bromination of propionic acid $(CH_3CH_2COOH)$ at the $\alpha$-carbon produces $2$-bromopropionic acid $(CH_3CH(Br)COOH)$. In $2$-bromopropion

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Optical isomers

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(B) The bromination of propionic acid $(CH_3CH_2COOH)$ at the $\alpha$-carbon produces $2$-bromopropionic acid $(CH_3CH(Br)COOH)$. In $2$-bromopropionic acid,the carbon atom attached to the bromine atom is a chiral center because it is bonded to four different groups: $-H$,$-CH_3$,$-Br$,and $-COOH$. Due to the presence of this chiral center,$2$-bromopropionic acid exists as two non-superimposable mirror images,which are known as enantiomers. Enantiomers are a type of optical isomer. Therefore,the pair of $2$-bromopropionic acids formed are optical isomers.

On bromination,propionic acid yields two isomeric $2$-bromopropionic acids. This pair is an important example of

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