Predict the product and explain the difference in reaction outcome. The image displays two chemical reactions involving hydrogenation of an alkyne group in a cyclic compound.1. **First Reaction:** - **Reactant:** A cyclic compound with an alkyne group (a triple bond) is shown. - **Reagent:** Hydrogen gas (H₂) and palladium (Pd) are used. - **Product:** The reaction likely results in the full hydrogenation of the alkyne to form an alkane, indicating that the triple bond is completely reduced to a single bond.2. **Second Reaction:** - **Reactant:** The same cyclic compound with an alkyne group as in the first reaction. - **Reagent:** Hydrogen gas (H₂) with a Lindlar Catalyst is used. - **Product:** The reaction results in the partial hydrogenation of the alkyne to form a cis-alkene, where the triple bond is reduced to a double bond, maintaining the cis configuration.### Explanation of the Catalysts:- **Palladium (Pd):** A catalyst used for complete hydrogenation of alkynes to alkanes, typically resulting in the saturation of the compound.- **Lindlar Catalyst:** A poisoned palladium catalyst that allows for the syn addition of hydrogen to alkynes, facilitating the formation of cis-alkenes without further reduction to alkanes.

Answered: Image /qna-images/answer/7c57d3f3-ecd6-4c6d-8054-cd0c448a4049.jpgThe difference in the reaction outcomes is that in first reaction H2 Pd is used that give the complete hydrogenation of double bond and triple bond product but when H2 and lindlar's catalyst is used the double bond remain as it is and triple bond is reduced to double bond with Z configuration