The Grignard reagent can be prepared by using magnesium in dry ether on |
$C_2H_5OH$ $C_2H_5Br$ $C_2H_6$ $C_2H_5NO_2$ |
$C_2H_5Br$ |
The correct answer is Option (2) → $C_2H_5Br$ Grignard reagents are prepared by reacting alkyl or aryl halides with magnesium metal in the presence of dry ether. General Reaction: $R-X + Mg \longrightarrow R-Mg-X$ (in dry ether) Detailed Explanation of Options Option 1: $C_2H_5OH$ (Ethanol) — Ethanol contains an acidic hydrogen attached to oxygen. Instead of forming a Grignard reagent, it reacts with magnesium to produce ethoxide or destroys any formed Grignard reagent via proton donation. Option 2: $C_2H_5Br$ (Ethyl bromide) — As an alkyl halide, it reacts readily with magnesium in dry ether to form ethyl magnesium bromide, which is a Grignard reagent. $C_2H_5Br + Mg \rightarrow C_2H_5MgBr$ Option 3: $C_2H_6$ (Ethane) — Ethane is an alkane and lacks a halogen atom. Since Grignard reagents require alkyl halides, ethane cannot react with magnesium to form one. Option 4: $C_2H_5NO_2$ (Nitroethane) — Nitro compounds do not form Grignard reagents; instead, they interfere with or react with the reagent due to their reactive functional group. |