Hello, Elijah,
a.) From the balanced equation we can write the calculation for Kp:
Kp = ([NO]2[Cl2])/[NOCl]2
For calculating the Kp, we can use the partial pressures of the gases for their concentrations. So enter the 3 values for partial pressures and solve for Kp.
Kp = ([1.25x10-3]2 [3x10-3])/[1.2]
Kp = 3.26 x10-9 with 3 sig figs. Check my calculation to be sure it is correct.
b.) We are asked what will happen to the partial pressure of Cl2 under a new set of conditions. We'll assume the Kp we calculated above is correct, and compare it to the result we get from doing the same calculation but using the new partial pressures.
Substitute the new partial pressures into the same equation and calculate the resulting "effective" Kp. I get a value of 5.33x10-9. This is higher than the actual Kp, so something must change to bring the number down, closer to 3.26x10-9. By looking at the original relationship, we see that [Cl2] appears in the numerator. So either it or the [NOCl] (or both) must decline. Absent any change in the NOCl partial pressure, we must conclude that the [Cl2] partial pressure must decline, so that the calculation moves closer to the true Kp.
I hope this helps,
Bob