The reaction in which a nucleophile replaces already existing nucleophile in a molecule is called nucleophilic substitution reaction. Haloalkanes are substrate in these reactions. In this type of reaction, a nucleophile reacts with haloalkane (the substrate) having a partial positive charge on the carbon atom bonded to halogen. A substitution reaction takes place and halogen atom, called leaving group departs as halide ion. Since the substitution reaction is initiated by a nucleophile, it is called nucleophilic substitution reaction. It is one of the most useful classes of organic reactions of alkyl halides in which halogen is bonded to sp3 hybridized carbon. |
What is the product formed when ethyl bromide reacts with KNO2? |
Nitro ethane Ethyl nitrite Ethyl nitrate No reaction |
Ethyl nitrite |
The correct answer is option 2. Ethyl nitrite. When ethyl bromide \((C_2H_5Br)\) reacts with potassium nitrite \((KNO_2)\), it undergoes a reaction known as the Finkelstein reaction under specific conditions. In this reaction, ethyl bromide is converted to ethyl nitrite \((C_2H_5ONO)\), not to be confused with ethyl nitrate. Finkelstein Reaction Ethyl bromide reacts with potassium nitrite in the presence of a polar solvent like acetone or DMF (Dimethylformamide). The reaction proceeds by nucleophilic substitution where the nitrite ion \((NO_2^-)\) acts as a nucleophile, replacing the bromine atom in ethyl bromide. This results in the formation of ethyl nitrite \((C_2H_5ONO)\).
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