JEE Main levelSingle correct optionDifficulty 2 of 3o1128
Acetaldehyde reacts with HCN and a trace of NaCN using only achiral reagents and solvent. The product mixture is
Aonly the (R)-enantiomer
Ban optically inactive racemic mixture of the two cyanohydrin enantiomers
Conly the (S)-enantiomer
Da single meso compound
Answer: B
The carbonyl carbon is planar, so CNX− attacks equally from both faces. The new stereocentre in CHX3−CH(OH)−CN is formed as a 1:1 mixture of (R) and (S), a racemate with no optical activity. A meso compound needs two stereocentres.