In which of the following reactions, major product is matched correctly?




This question concerns nucleophilic substitution reactions. Each option is analyzed to identify the correct major product.
1. Option 1: \( O\text{Na}^+ + \text{EtBr} \longrightarrow \text{OMe} \). This is incorrect. The nucleophile \( O\text{Na}^+ \) does not yield \( \text{OMe} \) when reacted with \( \text{EtBr} \). The expected product is \( \text{OEt} \), which conflicts with the stated reaction.
2. Option 2: \( \text{t-ButO}^-\text{Na}^+ + \text{EtBr} \longrightarrow \text{t-ButO}-\text{Et} \). This is incorrect. While \( \text{t-ButO}^- \) (tert-butoxide) undergoes nucleophilic substitution with \( \text{EtBr} \) to form \( \text{t-ButO}-\text{Et} \), this is not the major product typically observed in such reactions.
3. Option 3: \( O\text{Na}^+ + \text{nPrBr} \longrightarrow \text{O-nPr} \). This is the correct answer. The nucleophile \( O\text{Na}^+ \) reacts with \( \text{nPrBr} \) (n-propyl bromide) via nucleophilic substitution, displacing the bromide ion to form \( \text{O-nPr} \), which is the expected major product.
4. Option 4: \( \text{Sec ButO}K^+ + \text{EtBr} \longrightarrow \text{Sec But} - \text{OEt} \). This is incorrect. The expected product is \( \text{Sec ButO}-\text{Et} \), but its formation is unlikely under these reaction conditions and expected reaction type.
Therefore, Option 3 correctly matches the major product.
Given below are two statements:
Statement (I): Alcohols are formed when alkyl chlorides are treated with aqueous potassium hydroxide by elimination reaction.
Statement (II): In alcoholic potassium hydroxide, alkyl chlorides form alkenes by abstracting the hydrogen from the $ \beta $-carbon.
In the light of the above statements, choose the most appropriate answer from the options given below: