2-Pentyne, CH3−C≡C−C2H5, hydrogenated over Pd/C undergoes syn addition of hydrogen across the triple bond, placing both alkyl groups on the same side of the resulting double bond and giving cis-2-pentene; the starting alkyne here is A, 2-pentyne.
2-Butyne, CH3−C≡C−CH3, reduced with sodium in liquid ammonia goes through a radical-anion mechanism that adds hydrogen anti across the triple bond, placing the two methyl groups on opposite sides of the double bond and giving trans-2-butene as B.
JEE Main · 2024 · 01 Feb 2024 · Shift 2 · Single correct option