How would you distinguish between an aldehyde and a ketone in the laboratory?
Aldehydes, Ketones and Carboxylic Acids
Original Khojo Papers practice question — not from a past board paper.
A ketone has two alkyl groups attached to the carbonyl carbon while an aldehyde has one at most. The alkyl groups release electrons and reduce the positive charge on the carbonyl carbon, and they also crowd the approach of the nucleophile. Both effects make the ketone less reactive.
No citable source has been recorded for this record. Treat it as practice material, not as fact.
Formaldehyde, with no alkyl group at all, is the most reactive of them.
From the same topic and chapter, at a similar level.
How would you distinguish between an aldehyde and a ketone in the laboratory?
Aldehydes, Ketones and Carboxylic Acids
What is the iodoform test, and which compounds give a positive result?
Aldehydes, Ketones and Carboxylic Acids
Describe the aldol condensation and the Cannizzaro reaction, and say which aldehydes undergo each.
Aldehydes, Ketones and Carboxylic Acids
Arrange acetic acid, chloroacetic acid and trichloroacetic acid in increasing order of acidity and give the reason.
Aldehydes, Ketones and Carboxylic Acids
What is the van't Hoff factor, and what values does it take for sodium chloride and for acetic acid in benzene?
Solutions
Distinguish between Schottky and Frenkel defects and state the effect of each on density.
Solid State