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 Multiple Choice QuestionsLong Answer Type

111. Define vapour pressure of a liquid. What happens to the vapour pressure of a liquid when (a) a volatile solute dissolves in it and (b) a non-volatile solute dissolves in it?
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 Multiple Choice QuestionsShort Answer Type

112. What is osmotic pressure? How is it dependent on the number of moles of a solute?
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113. State Raoult’s law. If AT is the elevation of boiling point of a solvent and m is the number of moles of solute per kg of solvent, what is the realationship between T and m?
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114.

(a) What are non-ideal solution?
(b) What role does the molecular interaction play in deciding the vapour pressure of solutions (i) alcohol and kerosene (ii) Chloroform and acetone.


Answer:

When a solution does not obey Raoult’s law over the entire range of concentration, then it is called non-ideal solution.

(a) Non-ideal solutions are these solutions which
(i) do not follow Raoult’s law.
(ii) ΔHmix ≠ 0.
(iii) ΔVmix ≠ 0.
(iv) The force of attraction between A-A and B-B is not equal to A-B.

(b) In alcohol and acetone, force of attraction is less than alcohol and alcohol molecules as well as acetone and acetone molecule, therefore, vapour pressure increases.
In chlorofom and acetone, force of attraction increases due to intermolecular H-bonding, therefore, vapour pressure decreases.

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115. Why do colligative properties of an electrolyte solution of a given concentration are found to be larger than those of a non-electrolyte solution of the same concentration?
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116. Explain the following phenomena:
(i) Hemolysis
(ii) Crenation.
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117. Why do we observe abnormal molecular masses?
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118. How does osmotic pressure depend on molality of the solution?
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 Multiple Choice QuestionsLong Answer Type

119. The molar mass of acetic acid determined from the measurement of a colligative property is greater than its formula molar mass. Explain why?
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 Multiple Choice QuestionsShort Answer Type

120. Explain why solvent-solvent, solute-solute and solute-solvent interactions are important in determining the extent to which a solute dissolves in a solvent.
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