Respuesta :
Answer:
[tex]p_{SO_2} \approx 0 atm[/tex]
[tex]p_{O_2} = 0.52 - x = 0.26 atm[/tex]
[tex]p_{SO_3} = 2x = 0.52 atm[/tex]
Explanation:
The equilibrium system is defined by:
[tex]2 SO_2 (g) + O_2 (g)\rightleftharpoons 2 SO_3 (g)[/tex]
First of all, we need to be given the equilibrium constant for this reaction. Equilibrium constant is temperature-dependent. For the purpose of this problem and illustration of the thought process, we'll assume room temperature for which the equilibrium constant of this reaction is defined as:
[tex]K_{eq} = 4.3\cdot 10^6[/tex]
Define the equilibrium constant in terms of equilibrium molarities:
[tex]K_{eq} = \frac{p_{SO_3}^2}{p_{SO_2}^2p_{O_2}}[/tex]
Let's say that x atm of oxygen react, then, according to stoichiometry, 2x atm of sulfur dioxide react and 2x atm of sulfur trioxide are formed. The equilibrium amounts are then:
[tex]p_{SO_2} = 0.52 - 2x[/tex]
[tex]p_{O_2} = 0.52 - x[/tex]
[tex]p_{SO_3} = 2x[/tex]
Substitute into the K expression:
[tex]K_{eq} = 4.3\cdot 10^6 = \frac{(2x)^2}{(0.52 - 2x)^2(0.52 - x)}[/tex]
For such a huge equilibrium constant, we may assume that this reaction nearly goes to completion, so we'd have a limiting reactant, in which:
[tex]0.52 - 2x\approx 0[/tex]
This means:
[tex]x = 0.26 atm[/tex]
And the equilibrium partial pressures become:
[tex]p_{SO_2} \approx 0 atm[/tex]
[tex]p_{O_2} = 0.52 - x = 0.26 atm[/tex]
[tex]p_{SO_3} = 2x = 0.52 atm[/tex]