Given:
Weak dibasic acid H2A with Ka1=8.1×10−8 and Ka2=1.0×10−13
Initial concentration: [H2A]0=0.1 M
The solution also contains 0.1 M HCl, which dissociates completely to give [H+]0=0.1 M.
The main source of HA− is the first dissociation:
H2A⇌H++HA−
Let x be the amount of H2A that dissociates. Then at equilibrium:
[H2A]=0.1−x
[H+]=0.1+x
[HA−]=x
Applying the equilibrium expression:
Ka1=[H2A][H+][HA−]
8.1×10−8=0.1−x(0.1+x)(x)
Since Ka1 is very small and the common H+ ion from HCl suppresses dissociation, x≪0.1. Hence:
0.1−x≈0.1 and 0.1+x≈0.1
8.1×10−8≈0.1(0.1)(x)=x
Therefore:
[HA−]=x=8.1×10−8 M
The second dissociation (Ka2=1.0×10−13) is negligible compared to the first, so the HA− consumed in that step is insignificant.
Hence, the correct option is (3) 8.1×10−8 M.