CBSE TEST PAPER-04

CLASS - XII CHEMISTRY (Aldehydes, Ketones and carboxylic acids)

Topic:- Identification Question

1. A compound ‘A’ with formula C5H10O gives a positive 2, 4 –DNP test but a negative Tollen’s
test It can be oxidizing to carboxylic acid ‘B’ of molecular formula C3H6O2, when treated
with alk. KMnO4 under vigorous conditions. The salt of ‘B’ gives a hydrocarbon ‘C’ on
Kolbes’ electrolytic decarboxylation. Identify A,B.C & write chemical equations.

2. Acompound A with molecular formula C5H12O on oxidation forms compound B with

molecular formula C5H10O. The compound B gives iodoform test but does not reduce
ammoniacal silver nitrate. The compound B on reduction with Zn – Hg/ HCl gives compound
C with molecular formula C5H12. Identify A,B.C & give the chemical reactions involved.

3. An organic compound A, which has a characteristic odour, on treatment with NaOH forms two
compound B and C. Compound B has molecular formula C7H8O which on oxidation gives
back A. Compound C is the sodium salt of an acid. C, when heated with soda lime yields an
aromatic hydrocarbon D. deduce the structures of A to D.

4. C l2 / r e d P a lc . N H
CH 3
COOH (A ) 3
(B )

5. Br2/KOH NaNO2/HCl
C6H5CONH2 A B C
K2Cr2O7/H2SO4
+
6. KCN H2O/H PCl5
CH3Cl A B C

7. CH3COOH 
Ca(OH )2
→ (A) 
dry distribution
→ (B) 
I2 / NaOH
→(C)

alc .− KOH
8. CH 3COCH 3  → X 
LiAlH 4

SOCl2
→ Y   → Z

9. HC ≡ CH 
H 3O+ / HgSO4
→ A 
O
→ B 
Co ( OH )2
→C
10. Two moles of compound (A) on treatment with a strong base gives two compounds (B) and
(C). The compound (B) on dehydrogenation with Cu gives (A) while acidification of (C) gives
carboxylic acid (D) having molecular formula CH2O2. Identify (A) to (D).

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