Racemic compound has
Equimolar mixture of enantiomers
An equimolar mixture of enantiomers (dextro and leavo forms) is called racemic mixture. It is represented as dl form or form and is optically inactive.
An enantiomerically pure acid is treated with racemic mixture of an alcohol having one chiral carbon. The ester formed will be
During the debromination of meso-dibromobutane, the major compound formed will be
At room temperature the eclipsed and the staggered forms of ethane cannot be isolated because
The most unstable configuration of cyclohexane is
The type of isomerism shown by 6, 6-disitrodiphenic acid is
Meso-tartaric acid is optically inactive due to the presence of
How many carbon atoms in the molecule HOOC—(CHOH)2—COOH are asymmetric?
Racemic modification can be resolved by
Racemic tartaric acid is optically inactive due to
CH3CH2OH and CH3OCH3 are the examples of