Identify the product 'B' in the following reaction:
\(CH_3MgBr \xrightarrow{\text{Dry ice, Dry ether}} A \xrightarrow{\text{dil. HCl}, H_2O} B\)
Concept:
Grignard reagents (\(R-MgX\)) react with solid carbon dioxide (dry ice) to form an intermediate magnesium carboxylate complex. Upon subsequent acid hydrolysis, this complex yields a carboxylic acid with one more carbon atom than the original alkyl group in the Grignard reagent.
Step 1:
Identify the first step (Nucleophilic addition).
Methyl magnesium bromide (\(CH_3MgBr\)) acts as a nucleophile and attacks the electrophilic carbon of carbon dioxide (\(CO_2\), dry ice) in the presence of dry ether.
\[ CH_3MgBr + O=C=O \xrightarrow{\text{Dry ether}} CH_3-C(=O)-O^-MgBr^+ \]
This forms the intermediate product A, which is a magnesium acetate complex. Step 2:
Identify the second step (Acid Hydrolysis).
The intermediate A is then subjected to acid hydrolysis using dilute HCl and water. This protonates the carboxylate oxygen, yielding a carboxylic acid and a basic magnesium halide by-product.
\[ CH_3-COOMgBr + H_2O \xrightarrow{H^+} CH_3-COOH + Mg(OH)Br \]
The final organic product B is \(CH_3COOH\), which is ethanoic acid (also known as acetic acid).