When several equilibria share species, their equilibrium constants combine algebraically in step with however the reactions themselves are added, reversed, multiplied or divided.
Reversing a reaction inverts its constant. If the forward reaction xA+yB⇌lC+mD has equilibrium constant KC, the reverse reaction lC+mD⇌xA+yB has constant KC′=1/KC (swapping numerator and denominator inverts the ratio). This is why the constant for the dissociation of one mole of SO3 into SO2 and O2 is (1/K1)1/2, not simply 1/K1, when K1 is defined for the two-mole formation reaction 2SO2+O2⇌2SO3: dissociating one mole of SO3 is half of the reverse of the two-mole reaction, so its constant is the square root of the reverse constant, 1/K1.
Adding reactions multiplies their constants. If A⇌B has constant K1 and B⇌C has constant K2, then the sum reaction A⇌C (obtained by adding the two equations and cancelling the common intermediate B) has constant K=K1K2, because each intermediate species' concentration term cancels out of the product of the two separate expressions. Chained over three or more steps, this becomes K4=K1K2K3 for a four-species chain A⇌B⇌C⇌D compared against the single direct step A⇌D. …
Step 1. The given reaction H2S(g)⇌H2(g)+21S2(g) has KC=4×10−2.
Step 2 (part i).2H2S(g)⇌2H2(g)+S2(g) is the given reaction with every coefficient doubled, so its constant is KC squared: (4×10−2)2=16×10−4=1.6×10−3. …