Aldol Condensation
Aldol condensation requires compounds possessing:
Select the correct option:
🔒 Solution Hidden from View
Submit your answer to unlock the detailed step-by-step solution.
More oxygen organics Practice Questions
Aldol condensation requires:
Aldol condensation requires:
Oxidation of a primary alcohol with PCC (pyridinium chlorochromate) gives:
Oxidation of a primary alcohol with PCC (pyridinium chlorochromate) gives:
Phenol is a stronger acid than cyclohexanol because:
Phenol is a stronger acid than cyclohexanol because:
Benzaldehyde under concentrated NaOH undergoes Cannizzaro because:
Benzaldehyde under concentrated NaOH undergoes Cannizzaro because:
Relative electrophilicity: acid chloride > aldehyde > ketone > amide because:
Relative electrophilicity: acid chloride > aldehyde > ketone > amide because:
Base-catalyzed ester hydrolysis (saponification) proceeds by initial:
Base-catalyzed ester hydrolysis (saponification) proceeds by initial:
Selective oxidation of secondary alcohol to ketone without affecting primary alcohol in same molecul...
Selective oxidation of secondary alcohol to ketone without affecting primary alcohol in same molecul...
Acetal formation from aldehyde and alcohol is catalyzed by:
Acetal formation from aldehyde and alcohol is catalyzed by:
Ferric chloride test gives violet coloration with:
Ferric chloride test gives violet coloration with:
Ether cleavage by HI proceeds to give:
Ether cleavage by HI proceeds to give:
Baeyer–Villiger oxidation converts ketone to:
Baeyer–Villiger oxidation converts ketone to:
p-Nitrobenzoic acid vs benzoic acid acidity order:
p-Nitrobenzoic acid vs benzoic acid acidity order:
About This Question
- Subject
- chemistry
- Chapter
- oxygen organics
- Topic
- aldol condensation
- Difficulty
- Easy
- Year
- 2025
Solution
Correct Answer:
At least one α-hydrogen to form enolate
- Role of Base: In an Aldol reaction, dilute alkali (NaOH or KOH) is used to abstract a proton.
- α-Hydrogen: This proton must be taken from the carbon atom adjacent to the carbonyl group (the α-carbon).
- Intermediate: The loss of this proton creates a resonance-stabilized Enolate ion.
- Nucleophilicity: The enolate behaves as a nucleophile and attacks the carbonyl carbon of another aldehyde/ketone molecule.
- Requirement: Without at least one α-hydrogen, the enolate cannot form, and the reaction cannot proceed. For example, Methanal and Benzaldehyde do not undergo Aldol condensation (they undergo Cannizzaro instead).
This easy difficulty chemistry question is from the chapter oxygen organics, covering the topic of aldol condensation. It appeared in the 2025 exam.
Looking for more practice? Explore all chemistry questions or browse oxygen organics questions on RankGuru.