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Question: Phosphorus pentachloride is dissociating \(50\% \) at \({250^ \circ }C\) at total pressure of \(Patm...

Phosphorus pentachloride is dissociating 50%50\% at 250C{250^ \circ }C at total pressure of PatmPatm. If the equilibrium constant isKp{K_p}, then which of the following reactions is numerically correct?
A) Kp=3P{K_p} = 3P
B) P=3KpP = 3{K_p}
C) P=2Kp3P = \dfrac{{2{K_p}}}{3}
D) Kp=2P3{K_p} = \dfrac{{2P}}{3}

Explanation

Solution

We know that the equilibrium constant Kp{K_p} describes the ratio of product and reactant concentrations at equilibrium in terms of partial pressures.
The expression can be given as,
Kp=(PC)c(PD)d(PA)a(PB)b{K_p} = \dfrac{{{{\left( {{P_C}} \right)}^c}{{\left( {{P_D}} \right)}^d}}}{{{{\left( {{P_A}} \right)}^a}{{\left( {{P_B}} \right)}^b}}}
The equilibrium constant Kp{K_p} is related to the equilibrium constants in terms of molar concentration.
PAP_A, PBP_B, PCP_C and PDP_D are partial pressures of A, B, C and D respectively.

Complete step by step solution:
The dissociation equation of PCl5PC{l_5} can be written as,
PCl5PCl3+Cl2PC{l_5} \rightleftharpoons PC{l_3} + C{l_2}
It is given the value of X=0.5X = 0.5
Let us calculate the mole fractions of the components.
XPCl5=10.53×0.5=13{X_{PC{l_5}}} = \dfrac{{1 - 0.5}}{{3 \times 0.5}} = \dfrac{1}{3}
XPCl3=10.53×0.5=13{X_{PC{l_3}}} = \dfrac{{1 - 0.5}}{{3 \times 0.5}} = \dfrac{1}{3}
XCl2=10.53×0.5=13{X_{C{l_2}}} = \dfrac{{1 - 0.5}}{{3 \times 0.5}} = \dfrac{1}{3}
We know that the total pressure is P.
Kp=(PPCl3)(PCl2)(PPCl2)=(XPCl3×P)(XCl2×P)(XPCl2×P){K_p} = \dfrac{{\left( {{P_{PC{l_3}}}} \right)\left( {{P_{C{l_2}}}} \right)}}{{\left( {{P_{PC{l_2}}}} \right)}} = \dfrac{{\left( {{X_{PC{l_3}}} \times P} \right)\left( {{X_{C{l_2}}} \times P} \right)}}{{\left( {{X_{PC{l_2}}} \times P} \right)}}
Let we substitute the values in the above equation we get,
Kp=13×P×13×P13×P\Rightarrow {K_p}\, = \dfrac{{\dfrac{1}{3} \times P \times \dfrac{1}{3} \times P}}{{\dfrac{1}{3} \times P}}
On simplifying we get,
P=3Kp\Rightarrow P = 3{K_p}
Therefore,option B is correct.

Additional information:
We know that dissociation constant is an equilibrium constant which measures the tendency of a bigger object to separate reversibly into smaller components; the equilibrium constant also can be called ionization constant.
For a general reaction:
AxByxA+yB{A_x}{B_y} \rightleftharpoons xA + yB
The dissociation constant of the reaction is,
Kp=[A]x[B]y[AxBy]{K_p} = \dfrac{{{{\left[ A \right]}^x}{{\left[ B \right]}^y}}}{{\left[ {{A_x}{B_y}} \right]}}
The equilibrium concentrations of A, B are [A]\left[ A \right],[B]\left[ B \right], and [AxBy]\left[ {{A_x}{B_y}} \right].

Note:
The idea of the stability constant is applied in various fields of chemistry and pharmacology. In protein-ligand binding the stability constant describes the attraction among a protein and a ligand. A small stability constant indicates an addition strongly among the ligand. Within the case of antibody-antigen requisite the upturned equilibrium constant is engaged and is named affinity constant.
Using the equilibrium constant we can calculate the pHpH of the reaction,
Example:
Write the dissociation equation of the reaction.
HA+H2OH3O++AHA + {H_2}O\xrightarrow{{}}{H_3}{O^ + } + {A^ - }
The constant Ka{K_a} of the solution is 4×1024 \times {10^{ - 2}}.
The dissociation constant of the reaction Ka{K_a} is written as,
Ka=[H3O+][A][HA]{K_a} = \dfrac{{\left[ {{H_3}{O^ + }} \right]\left[ {{A^ - }} \right]}}{{\left[ {HA} \right]}}
Let us imagine the concentration of [H3O+][A]\left[ {{H_3}{O^ + }} \right]\left[ {{A^ - }} \right] as x.
4×107=x20.08x4 \times {10^{ - 7}} = \dfrac{{{x^2}}}{{0.08 - x}}
x2=4×107×0.08{x^2} = 4 \times {10^{ - 7}} \times 0.08
On simplifying we get,
x=1.78×104\Rightarrow x = 1.78 \times {10^{ - 4}}
The concentration of Hydrogen is 1.78×1041.78 \times {10^{ - 4}}
We can calculate the pHpH of the solution is,
pH=log[H+]=3.75pH = - \log \left[ {{H^ + }} \right] = 3.75
The pHpH of the solution is 3.753.75.