@adianadiadi is right - let's say we have an acid (HA) which dissociates into its conjugate base (A-). The dissociation reaction is:
HA --> A- + H+
Let's say there is
0% dissociation. That gives us:
HA --> A- + H+
100% --> 0%
Therefore [base]/[acid] or [A-]/[HA] is
0/100
Now let's say there is
10% dissociation. That gives us:
HA --> A- + H+
90% --> 10%
Therefore [base]/[acid] or [A-]/[HA] is
10/90
Now let's say there is
50% dissociation. That gives us:
HA --> A- + H+
50% --> 50%
Therefore [base]/[acid] or [A-]/[HA] is
50/50
It turns out that at
50% dissociation, we have a really intersting situation. The Henderson-Hasselbalch equation states:
pH = pKa + log ([base]/[acid])
What's really cool is that when half is in the acid form, and the other half is in the conjugate base form, the base:acid ratio cancels out!
pH = pKa + log(50/50)
pH = pKa + log(1)
pH = pKa + 0
pH = pKa
The significance of this is the half-equivalence point: basically at this point on a titration curve (the flat parts of the curve), the acid is 50% dissociated. And, if we measure the pH, we can figure out experimentally what its pKa value is! So this is really important because it helps us measure how strong a given acid is, essentially. In other words,
pH = pKa at the half-equivalence point. But I digress...
Finally, let's say there is
100% dissociation. That gives us:
HA --> A- + H+
0% --> 100%
Therefore [base]/[acid] or [A-]/[HA] is
100/0 (woops, that's not even a real number - that's probably why the question asks you to stop at 99%
).