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Question: The partial pressure of ethane over a solution of \[{\text{6}}{{.56 \times 1}}{{\text{0}}^{{\text{ -...

The partial pressure of ethane over a solution of 6.56×10 - 3g{\text{6}}{{.56 \times 1}}{{\text{0}}^{{\text{ - 3}}}}{\text{g}} ethane is 1 bar. If the solution contains 5.00×10 - 2g{\text{5}}{{.00 \times 1}}{{\text{0}}^{{\text{ - 2}}}}{\text{g}}of ethane then what shall be the partial pressure of the gas?

Explanation

Solution

In the above question, we have to find the partial pressure of ethane when mass of the ethane is given. Since we don’t have any direct relationship between partial pressure and mass of the substance, we will be using Henry’s law which gives us a relationship between partial pressure and mole fraction of the gas.
Formula Used-
p = KHχ{\text{p = }}{{\text{K}}_{\text{H}}}{{\chi }}
where p = partial pressure of the gas
KH{{\text{K}}_{\text{H}}}= Henry’s Law constant
χ{{\chi }}= mole fraction of the gas

Complete step by step answer:
From Henry's Law, we know that the pressure of the gas in the vapour state (p) is directly proportional to the mole fraction of the gas (χ{{\chi }}) in the solution. So,
pχ{\text{p}} \propto {{\chi }}
p = KHχ{\text{p = }}{{\text{K}}_{\text{H}}}{{\chi }} (equation 1)
We know that mole fraction can be expressed as:
χ=mM{{\chi = }}\dfrac{{\text{m}}}{{\text{M}}}
where χ{{\chi }}=mole fraction of the gas, m= given mas and M= Molar mass of the gas
So replacing the value of χ{{\chi }}in the equation 1 we get:
p = KHmM{\text{p = }}\dfrac{{{{\text{K}}_{\text{H}}}{\text{m}}}}{{\text{M}}}
Taking m to the left hand side of the equation we get:
pm = KHM\dfrac{{\text{p}}}{{\text{m}}}{\text{ = }}\dfrac{{{{\text{K}}_{\text{H}}}}}{{\text{M}}}
Since, KH{{\text{K}}_{\text{H}}}is the Henry’s Law constant and M is the molar mass of the ethane which is constant, so we will always get pm\dfrac{{\text{p}}}{{\text{m}}} ratio constant
Now, if p1p_1= partial pressure of ethane in first solution
m1m_1= mass of ethane in the first solution
p2p_2= partial pressure of ethane in second solution
m2m_2= mass of ethane in the second solution
So, we get:
p1m1 = p2m2\dfrac{{{{p_1}}}}{{{{m_1}}}}{\text{ = }}\dfrac{{{{p_2}}}}{{{{m_2}}}}
Placing the values given in the question, we get:
16.56×10 - 3 = p25.00×10 - 2\dfrac{{\text{1}}}{{{\text{6}}{{.56 \times 1}}{{\text{0}}^{{\text{ - 3}}}}}}{\text{ = }}\dfrac{{{{p_2}}}}{{{\text{5}}{{.00 \times 1}}{{\text{0}}^{{\text{ - 2}}}}}}
By cross-multiplication, we get
5.00×10 - 26.56×10 - 3=p2\dfrac{{{\text{5}}{{.00 \times 1}}{{\text{0}}^{{\text{ - 2}}}}}}{{{\text{6}}{{.56 \times 1}}{{\text{0}}^{{\text{ - 3}}}}}}{{ = p_2}}
p2=7.62 bar{{p_2 = 7}}{\text{.62 bar}}
\therefore The partial pressure of ethane in the second solution is 7.627.62 bar.

Note:
Henry’s Law is not a universal law, it has some exceptions. So, it is not applicable when:
The pressure of gas is too high or the temperature is too low.
The gas should undergo any changes in the solution.