Predict the % product formation in the given reaction :
To determine the % product formation in the given reaction, let's analyze the reaction step-by-step:

The reaction given is a dehydrohalogenation reaction involving the elimination of HBr from the compound using alcoholic KOH as a base. This type of reaction typically forms alkenes.
Let's look into the possible products:
Given the options provided:
The correct answer is X = 71%, Y = 29%, because product (X) is favored due to it being the more substituted alkene, consistent with Zaitsev's rule.
Therefore, the major product is (X) with a formation percentage of 71%, while the minor product is (Y) with a formation percentage of 29%.
The Miller indices of the shown lattice plane in a simple cubic Bravais lattice are :

The R/S configuration of C - 2 and C - 3 in the given molecule will be :