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Question: Hydrogenation of the above compound in the presence of poisoned Pd catalyst gives: ![](https://www...

Hydrogenation of the above compound in the presence of poisoned Pd catalyst gives:

a.) – an optically active compound
b.) – an optically inactive compound
c.) – a racemic mixture
d.) – a diastereomeric mixture

Explanation

Solution

In this question, we are given with the alkyne molecule that will be hydrogenated. It means that it will react in the presence of dihydrogen. Write the chemical reaction, and on the basis of the product formed we can decide the nature of the compound. It depends on the plane of symmetry.

Complete step by step solution:
Now, first we are given with the alkyne molecule. As mentioned, it undergoes hydrogenation in the presence of palladium.
So, we can say that it reacts with the dihydrogen, and if there is a poisoned palladium catalyst, then there will be presence of barium sulphate too.
Thus, we can write the chemical reaction for the given molecule, i.e.

Here, we can see that the hydrogenation of alkyne molecules leads to the formation of alkene molecules.
Now, if we talk about the nature of the product, then we see it has a plane of symmetry.
In the options, racemic mixture, and diastereomeric mixture is incorrect, as the product formed is only one.
Now, if the molecule has a plane of symmetry, then it is considered to be an optically inactive compound.
In the last we can conclude that the hydrogenation of the above compound in the presence of a poisoned Pd catalyst gives an optically inactive compound.

Hence, the correct option is (B).

Note: There could be confusion in the two options, i.e. optically active compound, and optically inactive compound. The optically active compound is the compound which represents no plane of symmetry, whereas the optically inactive compound is the compound which represents the plane of symmetry.