To determine the product of the reaction between alcoholic silver nitrite and ethyl bromide, let's understand the chemical process involved.
**Explanation of Reaction:**
- When ethyl bromide (C2H5Br) reacts with silver nitrite (AgNO2) in alcoholic medium, the reaction proceeds via nucleophilic substitution.
- Silver nitrite is ambidentate, meaning it can act as a nucleophile through either the nitrogen or oxygen atom. However, in this case, the nitrogen from silver nitrite attacks the ethyl group, leading to the formation of a nitro compound rather than a nitrite.
**Reaction Equation:**
\(\text{C}_2\text{H}_5\text{Br} + \text{AgNO}_2 \rightarrow \text{C}_2\text{H}_5\text{NO}_2 + \text{AgBr} \downarrow\)
Here, the bromine atom in ethyl bromide is replaced by the nitro group (NO2), resulting in nitro ethane (C2H5NO2).
**Conclusion:**
- The product of this reaction is nitro ethane.
- This results because the nitrogen acts as a nucleophile, leading to the formation of a nitro compound instead of an alkyl nitrite.
Thus, the correct answer is: nitro ethane.