The correct option is A Lindlar Catalyst
Lindlar catalyst →H2/Pd (CaCO3, Quinoline)
Here, the alkyne will undergo partial reduction to form cis-alkene. Both the H atom gets add to the alkyne in same direction to give cis- product.
Reduction of alkyne using Na/liq.NH3 is called Birch reduction. In this H gets add to the triple bond in opposite direction to give trans product.
Baeyer's reagent → Alkaline cold dil.KMnO4. This reagent oxides the alkene reactant by syn addition of OH.
It reacts with ethene to form Ethane-1,2-diol (glycol).