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Question: The lowering of vapour pressure of \[{\text{0}}{\text{.1M}}\] aqueous solutions of \({\text{NaCl}}\)...

The lowering of vapour pressure of 0.1M{\text{0}}{\text{.1M}} aqueous solutions of NaCl{\text{NaCl}} , CuSO4{\text{CuS}}{{\text{O}}_{\text{4}}} and K2SO4{{\text{K}}_2}{\text{S}}{{\text{O}}_{\text{4}}} are:
A.All equal
B.In the ratio of 1:1:1.51:1:1.5
C.In the ratio of 3:2:13:2:1
D.In the ratio of 1.5:1:2.51.5:1:2.5

Explanation

Solution

Relative lowering of vapour pressure is a colligative property as it is independent of the nature of the solute but is dependent on the moles of that solute.
For substances undergoing association or dissociation, the relative lowering of vapour pressure is equal to the van’t Hoff factor multiplied by mole fraction of solute.

Complete step by step answer:
The relation between the relative lowering of vapour pressure of a solution and the mole fraction of the non-volatile solute in the solution for substances undergoing association or dissociation is given by Raoult’s law and the expression for this law is given by:
p0 - psp0 = ix2\dfrac{{{{\text{p}}^{\text{0}}}{\text{ - }}{{\text{p}}_{\text{s}}}}}{{{{\text{p}}^{\text{0}}}}}{\text{ = i}}{{\text{x}}_2}
where p0{{\text{p}}^{\text{0}}} denotes the vapour pressure of the pure solvent, ps{{\text{p}}_{\text{s}}} denotes the vapour pressure of the solution, ‘i’ denotes the van’t Hoff factor.
So, the term p0 - ps{{\text{p}}^{\text{0}}}{\text{ - }}{{\text{p}}_{\text{s}}} represent the lowering of vapour pressure and p0 - psp0\dfrac{{{{\text{p}}^{\text{0}}}{\text{ - }}{{\text{p}}_{\text{s}}}}}{{{{\text{p}}^{\text{0}}}}} represent the relative lowering of vapour pressure and x2{{\text{x}}_{\text{2}}} represent the mole fraction of that solute.
Now, 0.1M{\text{0}}{\text{.1M}} aqueous solutions means 0.1{\text{0}}{\text{.1}} moles in one litre of solution and so mole fraction x2=0.1{{\text{x}}_{\text{2}}} = 0.1
Now, van’t Hoff factor is equal to the number of solute particles.
So, for NaCl{\text{NaCl}} , the van’t Hoff factor ‘i’ is equal to 2 as it dissociates into one sodium ion and one chloride ion.
NaClNa +  + Cl - {\text{NaCl}} \to {\text{N}}{{\text{a}}^{\text{ + }}}{\text{ + C}}{{\text{l}}^{\text{ - }}}
For CuSO4{\text{CuS}}{{\text{O}}_{\text{4}}} , van’t Hoff factor ‘i’ is equal to 2 as it dissociates into one copper (II) ion and one sulphate ion.
CuSO4Cu2 +  + SO42 - {\text{CuS}}{{\text{O}}_{\text{4}}} \to {\text{C}}{{\text{u}}^{{\text{2 + }}}}{\text{ + S}}{{\text{O}}_{\text{4}}}^{{\text{2 - }}}
For K2SO4{{\text{K}}_2}{\text{S}}{{\text{O}}_{\text{4}}} , van’t Hoff factor ‘i’ is equal to 3 as it dissociates into two potassium ions and one sulphate ion.
K2SO42K +  + SO42 - {{\text{K}}_2}{\text{S}}{{\text{O}}_{\text{4}}} \to 2{{\text{K}}^{\text{ + }}}{\text{ + S}}{{\text{O}}_{\text{4}}}^{{\text{2 - }}}
So, the lowering of vapor pressure for NaCl{\text{NaCl}} will be
p0 - psp0 = 2×0.1 = 0.2\dfrac{{{{\text{p}}^{\text{0}}}{\text{ - }}{{\text{p}}_{\text{s}}}}}{{{{\text{p}}^{\text{0}}}}}{\text{ = 2}} \times {\text{0}}{\text{.1 = 0}}{\text{.2}}
For CuSO4{\text{CuS}}{{\text{O}}_{\text{4}}}, it will be \dfrac{{{{\text{p}}^{\text{0}}}{\text{ - }}{{\text{p}}_{\text{s}}}}}{{{{\text{p}}^{\text{0}}}}}{\text{ = 2}} \times {\text{0}}{\text{.1 = 0}}{\text{.2}}\ For ${{\text{K}}_2}{\text{S}}{{\text{O}}_{\text{4}}}$ , it will be \[\dfrac{{{{\text{p}}^{\text{0}}}{\text{ - }}{{\text{p}}_{\text{s}}}}}{{{{\text{p}}^{\text{0}}}}}{\text{ = 3}} \times {\text{0}}{\text{.1 = 0}}{\text{.3}}
So, the required ratio is 0.2:0.2:0.30.2:0.2:0.3 or 1:1:1.51:1:1.5

So the correct option is (2).

Note:
If there is dissociation of the solute in the solution, then ‘i’ is greater than 1 and if there is association of the solute in the solution, then ‘i’ is less than 1.
The van’t Hoff factor ‘i’ is equal to the observed colligative property divided by the calculated colligative property.