J.R. S. answered 04/21/20
Ph.D. University Professor with 10+ years Tutoring Experience
Because the second dissociation constant (1.6x10-12) is more than 3 orders of magnitude less than the first dissociation constant (8.00x10-5), it can be ignored as far as making any meaningful contribution to the [H+], and hence has negligible effect on pH.
H2C6H6O6 ==> H+ + HC6H6O6-
Ka1 = 8.00x10-5 = [H+][HC6H6O6-]/[H2C6H6O6]
8.00x10-5 = (x)(x)/0.135 - x and assuming x is small compared to 0.135, it can be ignored in the denominator
x2 = 1.08x10-5
x = 3.29x10-3 M = [H+] (assumption above was correct as this is only 2.4% of 0.135 and so is negligible)
pH = -log 3.29x10-3 = 2.48
Equilibrium concentrations as follows:
[H2C6H6O2] = 0.135 - 0.00329 = 0.132 M
[HC6H6O6-] = 3.29x10-3 M
[C6H6O62-] = 7.3x10-8 M (see below)**
HC6H6O6- ==> H+ + C6H6O62-
1.6x10-12 = (x)(x)/3.29x10-3
x2 = 5.3x10-15
x = 7.3x10-8 M = equilibrium concentration of C6H6O62-