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Question: At temperature \[T{\text{ K, PC}}{{\text{l}}_5}\] is \[50\% \] dissociated at an equilibrium pressur...

At temperature T K, PCl5T{\text{ K, PC}}{{\text{l}}_5} is 50%50\% dissociated at an equilibrium pressure of 4 atm{\text{4 atm}}. At what pressure it would dissociate to the extent of 80%80\% at the same temperature?
A.0.05 atm{\text{0}}{\text{.05 atm}}
B.0.60 atm{\text{0}}{\text{.60 atm}}
C.0.75 atm{\text{0}}{\text{.75 atm}}
D.0.25 atm{\text{0}}{\text{.25 atm}}

Explanation

Solution

There is a direct relationship between degree of dissociation for dissociation of type AB+CA \to B + Cand total pressure at equilibrium; we are going to use the relation here. We will get two equations one for 50%50\% dissociation and other for 80%80\% dissociation. Degree of dissociation is in fraction so we need to convert the percentage into fraction. Dividing both the equations we will get the value of pressure.

Formula used: Kp=α2×PT(1α2){{\text{K}}_{\text{p}}} = \dfrac{{{\alpha ^2} \times {{\text{P}}_{\text{T}}}}}{{(1 - {\alpha ^2})}} for reaction of type AB+CA \to B + C
Where, α1{\alpha}_1 is degree of dissociation, KP{{\text{K}}_P} is equilibrium constant in terms of pressure, PT{{\text{P}}_{\text{T}}} is total pressure at equilibrium.

Complete step by step solution:
α is the degree of dissociation, it is the ratio of dissociated moles to the total no of moles of the reactant. KP{{\text{K}}_P} is equilibrium constant which is a function of temperature, if temperature remains constant then it will not change. Hence for both the dissociation KP{{\text{K}}_P} will remain the same as temperature is constant. To convert α into fraction we need to divide it with 100.
So α1{\alpha}_1 will be 50100=0.5\dfrac{{50}}{{100}} = 0.5 and pressure is given to us that is 4 atm{\text{4 atm}}.
Putting the above value in formula:
Kp=(0.5)2×4(1(0.5)2)=10.75{K_p} = \dfrac{{{{(0.5)}^2} \times 4}}{{(1 - {{(0.5)}^2})}} = \dfrac{1}{{0.75}}
Similarly α1{\alpha}_1 will be 80100=0.8\dfrac{{80}}{{100}} = 0.8
Kp=(0.8)2×Pt(1(0.8)2)=1.777Pt{K_p} = \dfrac{{{{(0.8)}^2} \times {{\text{P}}_{\text{t}}}}}{{(1 - {{(0.8)}^2})}} = 1.777{{\text{P}}_{\text{t}}}
Dividing or equating both the equation we will get:
10.75=1.7777Pt\dfrac{1}{{0.75}} = 1.7777{{\text{P}}_{\text{t}}}
Rearranging we will get the value of pressure:
Pt = 0.75 atm{{\text{P}}_{\text{t}}}{\text{ = 0}}{\text{.75 atm}}

Hence, option C is correct.

Note: The dissociation of PCl5{\text{PC}}{{\text{l}}_5} follows the following reaction: PCl5  PCl3 + Cl2 {\text{PC}}{{\text{l}}_{\text{5}}}{\text{ }} \rightleftharpoons {\text{ PC}}{{\text{l}}_3}{\text{ + C}}{{\text{l}}_2}{\text{ }}. As we can see that the number of moles of both the product is same, this implies that pressure of these reactants will be same at equilibrium and pressure of PCl5{\text{PC}}{{\text{l}}_5} will be different.
a{\text{a}} is initial moles of reactant and xx is amount of reactant dissociated. In this case α\alpha will be xa\dfrac{x}{{\text{a}}}.
time PCl5  PCl3 + Cl2 {\text{time PC}}{{\text{l}}_{\text{5}}}{\text{ }} \rightleftharpoons {\text{ PC}}{{\text{l}}_3}{\text{ + C}}{{\text{l}}_2}{\text{ }}