CBSE Class 12 Chemistry sample paper 2026-27: question 31(B)
From the official CBSE sample question paper for 2026-27, section E, question 31(B), for 5 marks. Try it first; the hints and our step-by-step solution are below.
Q31(B) · 5 marks · Long answerAldehydes, Ketones and Carboxylic Acids
(I) Arrange the following according to the property indicated (3x1)
a) , HCHO, (decreasing order of the ease of oxidation)
b) , , , (increasing order of nucleophilic acyl substitution)
c) , , (increasing order of electrophilicity of carbonyl carbon)
(II) Write any two possible isomers of the compound having molecular formula . Identify which of these isomer/s will give a positive Tollen’s test and explain the reason. (2)
Source: official sample paper from cbseacademic.nic.in (PDF). See it in the full Sample paper 2026-27.
Hints
Open one hint at a time and try again before the next.
Hint 1
Electron-donating groups make the carbonyl carbon less electrophilic; electron-withdrawing groups make it more so.
Hint 2
For acyl substitution, compare how good a leaving group each of Cl, OCH₃, OH and NH₂ is.
Hint 3
Tollens' reagent is a mild oxidant. Which carbonyl compounds have an oxidisable C–H on the carbonyl carbon?
Step-by-step solution
Each step shows the marks it earns, as an examiner would award them. Checked by an independent re-solve from the question paper.
- 1 mark
(I)(a) HCHO > CH₃CHO > C₆H₅CHO. The +I effect of the methyl group and the resonance of the phenyl ring progressively reduce the ease of oxidation.
- 1 mark
(I)(b) CH₃CONH₂ < CH₃COOH < CH₃COOCH₃ < CH₃COCl. Reactivity rises as the leaving group gets better and as its resonance donation to C=O gets weaker. is the best leaving group; donates strongly by resonance and is the poorest leaving group.
- 1 mark
(I)(c) CH₃COCH₃ < CH₃CHO < CF₃CHO. Two electron-donating methyls lower the electrophilicity, one methyl lowers it less, and the strongly –I group raises it the most.
- 1 mark
(II) Two isomers of : propanal, , and propanone, .
- 1 mark
Propanal gives a positive Tollens' test (silver mirror). Its aldehydic C–H allows it to be oxidised to propanoate, reducing to metallic Ag. Propanone, a ketone, has no such hydrogen and is not oxidised by this mild reagent.
Answer: (I)(a) HCHO > CH₃CHO > C₆H₅CHO; (b) CH₃CONH₂ < CH₃COOH < CH₃COOCH₃ < CH₃COCl; (c) CH₃COCH₃ < CH₃CHO < CF₃CHO; (II) propanal and propanone; propanal gives Tollens' test.
Where the marks are
- Correct order (a) (1 mark)
- Correct order (b) (1 mark)
- Correct order (c) (1 mark)
- Two correct isomers (½ + ½ mark)
- Propanal identified with reason (oxidation of aldehyde, Ag⁺ reduced to Ag) (½ + ½ mark)
Revise the chapter
- Chapter: Aldehydes, Ketones and Carboxylic Acids (notes, formulas, where marks are lost and every past question)
More questions from Aldehydes, Ketones and Carboxylic Acids
- 2026 board paper, set 56/1/1, Q26 · 3 marksGive reasons for the following : (a) Carboxylic acids have higher boiling point than alcohols of comparable mo…
- 2026 board paper, set 56/1/1, Q31(a) · 5 marks(i) An organic compound (X) has the molecular formula C_5H10O. Draw structures for (X) if it : (I) does not gi…
- 2026 board paper, set 56/1/1, Q31(b) · 5 marksAnswer the following questions : (i) Draw structure of the 2, 4-dinitrophenyl hydrazone derivative of benzalde…
The question is transcribed from the official paper; figures are described in words. The solution, hints and chapter tag are ours. Spotted an error? Write tosupport@questionbuddy.in.