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Explain the fact that in aryl alkyl ethers
- the alkoxy group activates the benzene ring towards electrophilic substitution and
- it directs the incoming substituents to ortho and para positions in the benzene ring.
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Why does O3 act as a powerful oxidising agent?
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How is O3 estimated quantitatively?
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Which aerosols deplete ozone?
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Determine the osmotic pressure of a solution prepared by dissolving 2.5 × 10−2 g of K2SO4 in 2L of water at 25°C, assuming that it is completely dissociated.
(R = 0.0821 L atm K−1 mol−1, Molar mass of K2SO4 = 174 g mol−1)
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Give the structures of A, B and C in the following reactions:

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Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger acid than phenol. Give two reasons.
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How would you account for the following:
The chemistry of actinoids is more complicated as compared to lanthanoids.
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Write the structures of main products when benzene diazonium chloride `(C_6H_5N_2^(+)Cl^-)`reacts with the following reagents:
CuCN/KCN
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Write the structures of main products when benzene diazonium chloride `(C_6H_5N_2^(+)Cl^-)`reacts with the following reagents:
H2O
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Write the structures of main products when benzene diazonium chloride `(C_6H_5N_2^(+)Cl^-)`reacts with the following reagents:
CH3CH2OH
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Give a reason for the following:
Actinoids show irregularities in their electronic configurations.
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Write the structures of A, B and C in the following:

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Why pKa of F-CH2-COOH is lower than that of Cl−CH2−COOH?
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What happens when the external pressure applied becomes more than the osmotic pressure of solution?
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Blood cells are isotonic with 0.9% sodium chloride solution. What happens if we place blood cells in a solution containing
(i) 1.2% sodium chloride solution?
(ii) 0.4% sodium chloride solution?
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How would you account for the following:
Actinoid contraction is greater than lanthanoid contraction.
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Why do actinoids show a wide range of oxidation states?
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Write on similarity between the chemistry of lanthanoids and actinoids.
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Distinguish between the following : Benzoic acid and methyl benzoate
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