J.R. S. answered 04/08/20
Ph.D. University Professor with 10+ years Tutoring Experience
The easy way to solve it is to ignore Ka2 since it is several orders of magnitude (>5) smaller than Ka1 and so it will not contribute to the generation of H+ ions. The more difficult way is to include it as explained below.
Ignoring Ka2:
H2SO3 ==> H+ + HSO3-
Ka = 0.017 = [H+][HSO3-]/[H2SO3]
0.017 = (x)(x)/0.15 - x
x2 = 0.00255 - 0.017x
x2 + 0.017x - 0.00255 = 0
x = 0.0497 M = [H+]
pH = -log 0.0497
pH = 1.3
If you wanted to include the second dissociation, you would have the following:
HSO3- ===> H+ + SO32-
0.0497.............0...........0.......Initial
-x...................+x...........+x........Change
0.0497-x.........x.............x........Equilibrium
Ka2 = 6.4x10-8 =(x)(x)/0.0497-x
Solve for x which will be [H+] form the second ionization. Add this to [H+] from first ionization (0.0497) and take negative log. The answer will be as close to 1.3 as anything within experimental error. But that's the way to do it.