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Question: When sulphur (in the form of \( {S_8} \) ) is heated to temperature T, at equilibrium, the pressure ...

When sulphur (in the form of S8{S_8} ) is heated to temperature T, at equilibrium, the pressure of S8 falls by 30% from 1.0 atm, because S8(g){S_8}(g) is partially converted into S2(g){S_2}(g) .Find the value of Kp{K_p} for this reaction.
(A) 2.96
(B) 6.14
(C) 204.8
(D)None of these

Explanation

Solution

Hint : Chemical equilibrium is a state where the rate of forward reaction becomes equal to the rate of backward reaction in case of reversible reactions. It is of dynamic nature. Concentration of the reactants and products becomes constant at Equilibrium. Equilibrium constant is the value of reaction quotient found as the ratio of Concentration of products and that of reactants. In a gaseous reaction where we have partial pressure then it is calculated as ratio of Concentration in terms of partial pressure of the products and the reactants (Kp)({K_p}) .

Complete Step By Step Answer:
Consider a reaction, aA(g)+bB(g)cC(g)+dD(g)aA(g) + bB(g) \rightleftharpoons cC(g) + dD(g)
The expression for Kp=[PC]c[PD][PA]a[PB]bd(1){K_p} = {\dfrac{{{{\left[ {{P_C}} \right]}^c}\left[ {{P_D}} \right]}}{{{{\left[ {{P_A}} \right]}^a}{{\left[ {{P_B}} \right]}^b}}}^d} - - - - (1)
Kp{K_p} is related to Equilibrium constant in terms of concentration as-
Kp=Kc(RT)Δn(2){K_p} = {K_c}{\left( {RT} \right)^{\Delta n}} - - - - (2)
Where Δn\Delta n is the difference in the number of moles of products and reactants.
In the question we are given a reaction as follows,
S8(g)4S2(g){S_8}(g) \rightleftharpoons 4{S_2}(g)

At time t=010
Partial pressure at Equilibrium1-x4x

{Since at time t=0, we have initial partial pressure of 1 atm and product partial pressure will be 0,now after some time reactant starts changing into product. The partial pressure of reactant decreases by an amount of x so the partial pressure of product will increase by 4x since 4 is the stoichiometric coefficient}
Given in the question, partial pressure falls by 30% from 1 atm means x=30/100=0.30
Now calculating Kp=[4x]41x=[4×0.30]410.30=[1.2]4atm40.7atm=2.96atm3{K_p} = \dfrac{{{{\left[ {4x} \right]}^4}}}{{1 - x}} = \dfrac{{{{\left[ {4 \times 0.30} \right]}^4}}}{{1 - 0.30}} = \dfrac{{{{\left[ {1.2} \right]}^4}at{m^4}}}{{0.7atm}} = 2.96at{m^3}
Hence option (A) is correct.

Note :
Kp{K_p} has the unit of pressure (i.e. atm or bar). Kp{K_p} can be calculated in Homogeneous as well as Heterogeneous Equilibria. For Example calculating Kp{K_p} in Haber’s process. It is important to note that Equilibrium constant depends on the mode of representation of reaction, temperature, change in pressure or the change in concentration of the reactants and product.