Assume 1 gmol feed basis
Let x be moles of O2 reacted
2 SO2 + O2 --> 2 SO3
Before: 0.1 0.9 0
IN: 0.1-2x 0.9-x 2x
Total moles 1-x
Mole frac.
[tex]
x_{SO_2}=\frac{0.1-2x}{1-x} \\
x_{O_2}=\frac{0.9-x}{1-x} \\
x_{SO_3}=\frac{2x}{1-x} \\
[/tex]
[tex]
P_{SO_2}=\frac{(0.1-2x)}{(1-x)}P \\
P_{O_2}=\frac{(0.9-x)}{(1-x)}P \\
P_{SO_3}=\frac{2x}{(1-x)}P \\
[/tex]
[tex]
K_p= \frac{P^2_{SO_3}}{ P^2_{SO_2} · P_{O_2} } \\
K_p=\frac{ 4x^2 . (1-x) .P }{ (0.1-2x)^2 . (0.9-x) } \\
[/tex]
P = 1.02bar. Kp = 65.1
Now you have only x as a variable. Solve.
[tex]
\frac{1.02}{65.1} = \frac{ 4x^2 . (1-x) }{ (0.1-2x)^2 . (0.9-x) }
[/tex]
That's a cubic; you ought to get three solutions.
Use x = 0.005305; find a good reason to throw the rest away..
[x seems a bit too small; Only 5% of the SO2 reacting away; makes me a bit suspicious I've some bug in my solution. ]Leave it to you to calculate the partial pressures.
Now, you can hope that I've not messed up my arithmetic.....But I'm pretty sure I have (especially since I already found and corrected 3 mistakes; there's probably more). So redo it yourself!