Question:

Identify the product(s) of the following two reactions (i) and (ii):

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The nucleophilic substitution reaction with NaI/acetone favors an SN2 mechanism, leading to the replacement of a halide (Br) by an iodide (I) group.
Updated On: Apr 15, 2025
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The Correct Option is B

Solution and Explanation

In reaction (i), the reaction with NaI/acetone leads to a nucleophilic substitution of the bromine atom by the iodide ion, forming the product \( \text{Me} - \text{C} - \text{CH}_2 - \text{I} \). In reaction (ii), a similar substitution occurs, but the iodide replaces the bromine atom, leading to the product \( \text{Me} - \text{C} - \text{CH} - \text{I} \).
Thus, the correct product from both reactions is an iodide substitution on the alkyl chain.
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