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Question: 1 mole \({A_X}{B_Y}\) when added to \(1.08kg\) of water, lowers its vapor pressure by \(35torr\) to ...

1 mole AXBY{A_X}{B_Y} when added to 1.08kg1.08kg of water, lowers its vapor pressure by 35torr35torr to 700torr700torr . If further 1184g1184g of methanol is added, then the vapor pressure increases by 37torr37torr . Considering only a few vapors are formed, and AXBY{A_X}{B_Y} is a non-volatile solute. What is the value of aa if the vapor pressure of pure methanol is a×102torra \times {10^2}torr .

Explanation

Solution

The relative lowering in the vapor pressure is a colligative property which depends on the relative number of particles of solute and does not depend upon the nature of the particles. The colligative properties are directly proportional to the mole fraction of solute and thus, on the number of moles of solute.

Complete step by step answer:
According to the relative lowering of vapor pressure, it is equal to the mole fraction of the solute. Mathematically, it can be written as:
PoPPo=x\dfrac{{{P^o} - P}}{{{P^o}}} = x….(i)
Where, Po={P^o} = Vapor pressure of pure solvent
P=P = Vapor pressure of the solution
x=x = mole fraction of the solute
Molar mass of water = H2O=18{H_2}O = 18
Molar mass of methanol = CH3OH=32C{H_3}OH = 32
Number of moles = n=wgivenMwn = \dfrac{{{w_{given}}}}{{{M_w}}}
Mole fraction = x=nn+Nx = \dfrac{n}{{n + N}}
Where, n=n = moles of solute
N=N = moles of solvent
Number of moles of water = 1.08×100018=60moles\dfrac{{1.08 \times 1000}}{{18}} = 60moles
Number of moles of methanol = 1.184×100032=37moles\dfrac{{1.184 \times 1000}}{{32}} = 37moles
When only the solute AXBY{A_X}{B_Y} is added to the water, the equation (i) becomes,
PoPPo=x\Rightarrow \dfrac{{{P^o} - P}}{{{P^o}}} = x
735700735=11+60=0.0164\Rightarrow \dfrac{{735 - 700}}{{735}} = \dfrac{1}{{1 + 60}} = 0.0164…. (ii)
When methanol is also added in the solution, then equation (i) becomes,
Po700Po=11+60+37=0.0102\Rightarrow \dfrac{{{P^o} - 700}}{{{P^o}}} = \dfrac{1}{{1 + 60 + 37}} = 0.0102
Thus, Po=745torr{P^o} = 745torr
But, this value of vapor pressure corresponds to only a mixture of methanol and water.
Let PP' be the partial vapor pressure of methanol in this mixture. From Dalton’s law of partial pressure, we have:
Ptotal=PAxA+PBxB{P_{total}} = {P_A}{x_A} + {P_B}{x_B} … (iii)
Where, Ptotal={P_{total}} = Total vapor pressure of the mixture = 745torr745torr
PA={P_A} = partial pressure of water = 735torr735torr
PB={P_B} = partial pressure of methanol = PP'
xA={x_A} = mole fraction of water = 6037+60=6097\dfrac{{60}}{{37 + 60}} = \dfrac{{60}}{{97}}
xB={x_B} = mole fraction of methanol = 3737+60=3797\dfrac{{37}}{{37 + 60}} = \dfrac{{37}}{{97}}
Substituting these values in (iii), we have:
745=735×6097+P×3797\Rightarrow 745 = 735 \times \dfrac{{60}}{{97}} + P' \times \dfrac{{37}}{{97}}
P=761torr8×102torr\Rightarrow P' = 761torr \approx 8 \times {10^2}torr
Comparing this value with the given value of a×102a \times {10^2} , we have the value of a=8a = 8 .

Note:
When a non-volatile solute is dissolved in a pure solvent, the vapor pressure of the solvent is lowered i.e. the vapor pressure of a solution is always lower than the vapor pressure of a pure solvent, because the escaping tendency of solvent molecules decreases (due to lesser solvent molecules per unit surface area).