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Question: Calculate the depression in the freezing point of water when \(10g\) of \(C{H_3}C{H_2}CHClCOOH\) is ...

Calculate the depression in the freezing point of water when 10g10g of CH3CH2CHClCOOHC{H_3}C{H_2}CHClCOOH is added to 250g250g of water.
[Ka=1.4×103,Kf=1.86kgmol1{K_a} = 1.4 \times {10^{ - 3}},Kf = 1.86kg\,\,mo{l^{ - 1}}]

Explanation

Solution

When a non-volatile solute is added in a solvent, its freezing point decreases from the actual value, this phenomenon is known as freezing point depression. This is because the chemical potential of the solvent in pure solvent is higher than in the mixture solvent.

Complete step by step answer:
To calculate the freezing point of water when 10g10g of CH3CH2CHClCOOHC{H_3}C{H_2}CHClCOOH is added to 250g250g of water, we need the formula:
ΔTfO=ikfm\Delta TfO = i\,k\,f\,m
Given, Ka=1.4×103{K_a} = 1.4 \times {10^{ - 3}}
Kf=1.86kgmol1Kf = 1.86kg\,\,mo{l^{ - 1}}
Weight of solute=10g = 10g
Weight of solvent=250g = 250g
Therefore, molecular weight of the soluteCH3CH2CHClCOOH \Rightarrow C{H_3}C{H_2}CHClCOOH
=4(12)+7(1)+2(16)+35.5= 4\left( {12} \right) + 7\left( 1 \right) + 2\left( {16} \right) + 35.5
=48+7+32+35.5= 48 + 7 + 32 + 35.5
=122.5g/mol= 122.5g/mol
According to the formula given above, we know the value of KfKf, but we need to find the value of ii and mm.
Calculation of mm i.e. molality:
Molality = Weight of solute×1000Molecular weight of solute×weight of solvent{\text{Molality = }}\dfrac{{{\text{Weight of solute}} \times {\text{1000}}}}{{{\text{Molecular weight of solute}} \times {\text{weight of solvent}}}}
Therefore,
m = 10×1000122.5×250{\text{m = }}\dfrac{{10 \times {\text{1000}}}}{{122.5 \times 250}}
m = 0.3265molkg1{\text{m = 0}}{\text{.3265}}mol\,k{g^{ - 1}}
Calculation of ii i.e. Van’t Hoff factor:
Let α=Degree of dissociation of the acid\alpha \, = \,{\text{Degree of dissociation of the acid}}
CH3CH2CHClCOOH+H2OCH3CH2CHClCOO+H2OC{H_3}C{H_2}CHClCOOH + {H_2}O \rightleftharpoons C{H_3}C{H_2}CHClCO{O^ - } + {H_2}{O^ \oplus }

Initial concentration:CCOO ++ OO
Concentration at equilibrium:CCαC - C\alpha CαC\alpha ++ CαC\alpha

We know, Kα=Concentration of productsConcentration of reactantsK\alpha = \dfrac{{{\text{Concentration of products}}}}{{{\text{Concentration of reactants}}}}
Kα=[Cα][Cα]CCαK\alpha = \dfrac{{\left[ {C\alpha } \right]\left[ {C\alpha } \right]}}{{C - C\alpha }}
As, α\alpha is very small with respect to 11, 1α=11 - \alpha = 1
Kα=Cα2K\alpha = C{\alpha ^2}
α=KαC\alpha = \sqrt {\dfrac{{K\alpha }}{C}}
On putting the values,
α=1.4×1030.3265\alpha = \sqrt {\dfrac{{1.4 \times {{10}^{ - 3}}}}{{0.3265}}}
α=0.065\alpha = 0.065
At equilibrium,
CH3CH2CHClOHCH3CH2CHClCOO+HC{H_3}C{H_2}CHClOH \rightleftharpoons C{H_3}C{H_2}CHClCO{O^ - } + {H^ \oplus }

Initial moles:11OO ++ OO
Final moles:1α1 - \alpha α\alpha ++ α\alpha

Therefore, total moles at equilibrium
=1α+α+α= 1 - \alpha + \alpha + \alpha
=1+α= 1 + \alpha
Therefore, Van’t Hoff factor, ii
i=1+α1i = \dfrac{{1 + \alpha }}{1}
1+0.065=1.0651 + 0.065 = 1.065
Hence, depression in freezing point is ΔTf\Delta Tf
ΔTf=ikfm\Delta Tf = i\,k\,f\,m
=1.065×1.86×0.3265= 1.065 \times 1.86 \times 0.3265
ΔTf=0.647C\Delta Tf = {0.647^\circ }C

Note: The lowering or depression in freezing point is because when a non-volatile solute adds to a volatile liquid solvent, then the vapour pressure of the solution becomes lower than that of the original or pure solution. So, the solids reach at an equilibrium with the solution at lower temperature.