But-2-yne (CH3−C≡C−CH3) undergoes partial hydrogenation.
Reaction with Pd/C (Lindlar-like conditions for 1 mole H2) gives cis-but-2-ene as product X.
Reaction with Na/liq.NH3 (Birch reduction) gives trans-but-2-ene as product Y.
Statement A: X (cis) and Y (trans) are geometrical isomers, hence stereoisomers. This is correct.
Statement B: Cis-but-2-ene (X) has a non-zero dipole moment (μ=0) due to the additive nature of bond moments, while trans-but-2-ene (Y) has zero dipole moment (μ=0) due to symmetry. Thus, statement B is incorrect.
Statement C: Cis-isomers generally have higher boiling points than trans-isomers due to higher dipole-dipole interactions. So, B.P. of X>Y. This is correct.
Statement D: Reductive ozonolysis (O3/Zn,H2O) of both cis-but-2-ene and trans-but-2-ene yields the same product, ethanal (CH3CHO). Thus, statement D is incorrect.
The incorrect statements are B and D.
