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CHCl(3)+MeCOMe overset(OH^(-))rarr A ove...

`CHCl_(3)+MeCOMe overset(OH^(-))rarr A overset("excess KOH")rarr B overset(NaOH - CaO)rarr C overset("KOBr")rarr D`

A

`MeCH_(2)OH`

B

`MeCOOH`

C

`Me_(2)CHOH`

D

`CH_(2)Cl_(2)`

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The correct Answer is:
To solve the problem step by step, we will analyze the reactions mentioned in the question. ### Step 1: Reaction of CHCl₃ with MeCOMe (acetone) - **Reactants**: CHCl₃ (chloroform) and MeCOMe (acetone). - **Reaction**: When chloroform reacts with acetone in the presence of a base (OH⁻), the nucleophilic attack occurs. The base deprotonates the acetone, allowing the negatively charged oxygen to attack the carbon of chloroform, leading to the formation of a compound A. - **Product A**: The product formed is a compound where the chloroform has been converted into a carbonyl compound with a trichloroethyl group. This can be represented as CH₃C(Cl)₂CCl₃. ### Step 2: Reaction of A with excess KOH - **Reactant**: Compound A from Step 1. - **Reaction**: In the presence of excess KOH, the chlorine atoms in compound A will be substituted by hydroxyl (OH) groups. This is a nucleophilic substitution reaction where the base replaces the chlorine atoms. - **Product B**: The final product after this reaction will be a triol (with three hydroxyl groups) on the carbon skeleton. However, this triol is unstable and will dehydrate to form a carboxylic acid. - **Final Product B**: CH₃C(OH)₂COOH (which can further dehydrate to form CH₃COOH). ### Step 3: Reaction of B with NaOH and CaO (Soda Lime) - **Reactant**: Compound B from Step 2. - **Reaction**: The reaction with NaOH and CaO is a decarboxylation reaction. Soda lime (NaOH + CaO) removes CO₂ from the carboxylic acid group. - **Product C**: The product will be an alkane (specifically, an ethane derivative) after the removal of CO₂. This can be represented as CH₃CH₃ (ethane). ### Step 4: Reaction of C with KOBr - **Reactant**: Compound C from Step 3. - **Reaction**: The reaction with KOBr (potassium hypobromite) leads to a haloform reaction. In this reaction, a methyl ketone (if present) will yield bromoform (CHBr₃) and acetic acid (CH₃COOH). - **Product D**: The product formed will be bromoform (CHBr₃) and acetic acid (CH₃COOH). ### Final Result - **Product D**: The final product D is bromoform (CHBr₃) along with acetic acid (CH₃COOH). ### Summary of Products - A: CH₃C(Cl)₂CCl₃ - B: CH₃C(OH)₂COOH - C: CH₃CH₃ - D: CHBr₃ and CH₃COOH (acetic acid)
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