Racemic tartaric acid is optically inactive due to
Racemic tartaric acid is optically inactive due to external compensation. Racemic tartaric acid is an equimolar mixture of optically active d- and l- forms. This form of tartaric acid is optically inactive due to external compensation.
The specific rotation of a pure enantiomer is + 16o. Its observed rotation if it is isolated from a reaction with 25% recemisation and 75% retention is
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 compound has