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Identify A and B in the given reaction ...

Identify A and B in the given reaction
`(A) overset("Dil. "H_(2)SO_(4)//HgSO_(4))rarr underset("(unstable)")underset("vinyl alcohol")({:(CH_(2)),("||"),("CHOH"):})rarr(B)`

A

`C_(2)H_(2) and CH_(3)CHO`

B

`CH_(2) and HCOOH`

C

`C_(2)H_(4) and CH_(3)COOH`

D

`C_(2)H_(2) and CH_(3)COOH`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we need to identify compounds A and B in the given reaction sequence. The reaction involves the treatment of a compound A with dilute H₂SO₄ and HgSO₄, leading to an unstable enol (vinyl alcohol), which then tautomerizes to form compound B. ### Step-by-Step Solution: 1. **Identify the Starting Compound (A)**: - The reaction begins with a compound that, when treated with dilute H₂SO₄ and HgSO₄, produces an enol. - This suggests that compound A is likely an alkyne, as alkynes can undergo hydration in the presence of these reagents to form enols. - The simplest alkyne is acetylene (C₂H₂). **Hint**: Look for a compound that can form an enol upon hydration, typically an alkyne. 2. **Reaction with Dilute H₂SO₄ and HgSO₄**: - When acetylene (C₂H₂) is treated with dilute H₂SO₄ and HgSO₄, the reaction involves the addition of water across the triple bond. - This results in the formation of an enol, specifically vinyl alcohol (CH₂=CHOH). **Hint**: Remember that the presence of HgSO₄ facilitates the addition of H and OH across the triple bond of the alkyne. 3. **Identify the Enol (Vinyl Alcohol)**: - The unstable enol formed is CH₂=CHOH, which is known as vinyl alcohol. - This compound is unstable and will undergo tautomerization. **Hint**: Tautomerization is a process where an enol converts to a more stable form, typically a carbonyl compound. 4. **Tautomerization to Form Compound B**: - Vinyl alcohol (CH₂=CHOH) undergoes tautomerization to form acetaldehyde (CH₃CHO). - This process involves the migration of a hydrogen atom and the conversion of the double bond from the carbon-oxygen bond to a carbon-carbon bond. **Hint**: Tautomerization often results in the formation of a more stable compound, such as an aldehyde or ketone. 5. **Final Identification**: - Therefore, we conclude that: - Compound A is acetylene (C₂H₂). - Compound B is acetaldehyde (CH₃CHO). ### Summary: - **A**: Acetylene (C₂H₂) - **B**: Acetaldehyde (CH₃CHO)
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