To identify acid D in the reaction, we analyze each step:
- Step 1: Ethyl bromide \(C_2H_5Br\) undergoes dehydrohalogenation with alcoholic KOH to form an alkene, ethylene \(C_2H_4\):
\(C_2H_5Br \xrightarrow[]{alc.\,KOH} C_2H_4\) - Step 2: Ethylene \(C_2H_4\) reacts with bromine \(Br_2\) in carbon tetrachloride \(CCl_4\) to yield 1,2-dibromoethane \(BrCH_2CH_2Br\):
\(C_2H_4 + Br_2 \xrightarrow[]{CCl_4} BrCH_2CH_2Br\) - Step 3: 1,2-Dibromoethane \(BrCH_2CH_2Br\) reacts with excess KCN via substitution, replacing bromine with cyanide groups to form ethylene cyanide \(NCCH_2CH_2CN\):
\(BrCH_2CH_2Br + 2KCN \rightarrow NCCH_2CH_2CN\) - Step 4: Hydrolysis of ethylene cyanide \(NCCH_2CH_2CN\) with excess water and acid \(H_3O^+\) converts nitrile groups to carboxylic acid groups, forming succinic acid \(HOOCCH_2CH_2COOH\):
\(NCCH_2CH_2CN \xrightarrow[]{H_3O^+} HOOCCH_2CH_2COOH\)
Therefore, acid D formed is Succinic acid.
The correct answer is Succinic acid.