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A : 6-oxoheptanal on treatment with dilute NaOH gives 1-cetylcyclopentene.  
R : In intramolecular aldol condensation, the Carbanion should be formed from α-carbon of ketone and it attacks on aldehydic carbon to form finally α-β unsaturated carbonyl compound. 
  • a)
    If both Assertion & Reason are true and the Reason is the correct explanation of the Assertion.
  • b)
    If both Assertion & Reason are true but the Reason is not the correct explanation of the Assertion.
  • c)
    If Assertion is true statement but Reason is false.
  • d)
    If Assertion is false statement but Reason is true. 
Correct answer is option 'A'. Can you explain this answer?
Most Upvoted Answer
A :6-oxoheptanal on treatment with dilute NaOH gives 1-cetylcyclopente...
The α-carbon of the aldehyde or ketone and the nucleophile should attack the carbonyl carbon. In this case, the α-carbon of 6-oxoheptanal is the 6th carbon, and the nucleophile attacks the carbonyl carbon to form the carbanion. Therefore, statement R is correct.
Community Answer
A :6-oxoheptanal on treatment with dilute NaOH gives 1-cetylcyclopente...
Not cetylcyclopentene but acetyl cyclopentene is the product
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A :6-oxoheptanal on treatment with dilute NaOH gives 1-cetylcyclopentene. R : In intramolecular aldol condensation, the Carbanion should be formed from α-carbon of ketone and it attacks on aldehydic carbon to form finally α-β unsaturated carbonyl compound.a)If both Assertion & Reason are true and the Reason is the correct explanation of the Assertion.b)If both Assertion & Reason are true but the Reason is not the correct explanation of the Assertion.c)If Assertion is true statement but Reason is false.d)If Assertion is false statement but Reason is true.Correct answer is option 'A'. Can you explain this answer?
Question Description
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