Step 1: Understanding the Concept:
The cyanide ion is an ambident nucleophile, meaning it can attack through carbon or through nitrogen. Ionic cyanides (KCN) attack through carbon and give nitriles. Covalent AgCN attacks through nitrogen.
Step 2: Detailed Explanation:
\[ \text{R-X} + \text{AgCN} \to \text{R-NC} + \text{AgX} \]
So alcoholic silver cyanide gives alkyl isocyanide.
Step 3: Why the other options are wrong.
Alcoholic \(\text{NH}_3\) gives amines. \(\text{KNO}_2\) gives alkyl nitrite mainly, and \(\text{AgNO}_2\) gives nitroalkane.
Final Answer:
The reagent is alcoholic AgCN, option (A).
\[ \boxed{\text{AgCN (alco)}} \]