you need the equation for kp
https://chem.libretexts.org/Core/Physical_and_Theoretical_Chemistry/Equilibria/Chemical_Equilibria/The_Equilibrium_Constant/Calculating_An_Equilibrium_Concentration_From_An_Equilibrium_Constant/Calculating_An_Equilibrium_Constant%2C_Kp%2C_Using_Partial_Pressures
you need to use an ice table
https://en.wikipedia.org/wiki/RICE_chart
https://www.youtube.com/watch?v=tT-2xk9ZG_A
etc
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you also need to recognize that for ideal gases at constant T and V, the coefficients of the balanced equation can be read as MOLE ratios... AND... as PRESSURE ratios
this
.. 1 CO2(g) + 1 C(s) <----> 2 CO(g)
means
.. 1 mole CO2 yields 2 mole CO
AND
.. 1 atm CO2 yields 2 atm CO
why? from the ideal gas law
.. PV = nRT
.. P/n = RT/V
if T/V is a constant.. (and R is a constant) we can write
.. P1/n1 = RT/V = P2/n2
or
.. P1/n1 = P2/n2
or
.. P1/P2 = n1/n2
i.e..
.. pressure ratios = mole ratios
anyway.. one last hint... ONE possibility is that the reaction is driven to the right..
so that some CO2 is consumed to produce some CO
.. .. .. . . .. .. ..CO2.. .. . .. .. . CO
Initial.. . .. .. ..1.35.. .. .. .. .. ..3.50
Change.. .. ..-X.. .. .. .. . ... .+2X.. . . .. based on coeff of balanced equation, X CO2 ---> 2X CO
Equilibrium..1.35 - X.. ... .. . 3.50 + 2x
so that
.. ... .. . [3.50 + 2x]²
.. Kp = ---- ---- ----- = 1.50
.. .. . .. .[1.50 - X]¹
another possibility is that the reaction is shifted to the left
so that some CO is consumed to produce some CO2
.. .. .. . . .. .. ..CO2.. .. . .. .. . CO
Initial.. . .. .. ..1.35.. .. .. .. .. ..3.50
Change.. .. ..+X.. .. .. .. . ... .-2X.. . . .. based on coeff of balanced equation, X CO2 ---> 2X CO
Equilibrium..1.35 + X.. ... .. . 3.50 - 2x
so that
.. ... .. . [3.50 - 2x]²
.. Kp = ---- ---- ----- = 1.50
.. .. . .. .[1.50 + X]¹
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you get to finish.. solve for X.. calculate values at equilibrium