Lindlar’s catalyst is used for the hydrogenation of alkynes to cis-alkenes. This catalyst is specifically designed to selectively hydrogenate alkynes without reducing them to alkanes. It does this by allowing the addition of hydrogen across the triple bond to form a cis-alkene.
In the given reactions:
- Option (A): This is a typical hydrogenation reaction, but it is not a case where Lindlar's catalyst is used.
- Option (B): This reaction involves the reduction of a ketone to an alcohol, which does not require Lindlar's catalyst.
- Option (C): This reaction involves the reduction of a nitro group to an amine, which also does not require Lindlar's catalyst.
- Option (D): This is a reduction of an aldehyde to a primary alcohol, which does not involve Lindlar’s catalyst.
- Option (E): This reaction shows the hydrogenation of an alkyne (
CH3C=CCH3) to a cis-alkene (
CH3CH=CHCH3), which is exactly the type of reaction Lindlar's catalyst is used for.
Thus, the correct answer is option (E),
CH3C=CCH3+H2→CH3CH=CHCH3. Quick Tip: Lindlar’s catalyst is specifically used for the partial hydrogenation of alkynes to form cis-alkenes. It is useful when selective reduction is required without reducing the alkyne all the way to an alkane.