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However, if a strong base is used to titrate a weak acid, the pH at the
equivalence point will not be 7. There is a lag in reaching the equivalence
point, as some of the weak acid is converted to its conjugate base. You should
recognize the pair of a weak acid and its conjugate base as a buffer. In
, we see the resultant lag that precedes the equivalence point,
called the buffering region. In the buffering
region, it takes a large
amount of NaOH to produce a small change in the pH of the receiving solution.
Figure %: Titration curve of a strong base titrating a weak acid
Because the conjugate base is basic, the pH will
be greater than 7 at the
equivalence point.
You will need to calculate the pH using the Henderson-Hasselbalch
equation, and inputting the
pKb and concentration of the
conjugate base of the weak acid.
The titration of a base with an acid produces a flipped-over version of the
titration curve of an acid with a base. pH is decreased upon addition of
the acid.
Note that the pH of a solution at the equivalence point has nothing
to do with the volume of
titrant necessary to reach the equivalence point; it is a property inherent to
the composition of the solution. The pH at the
equivalence point is calculated in
the same manner used to calculate the pH of weak base solutions in
Calculating pH's.
When polyprotic acids are titrated with strong bases, there
are multiple equivalence points. The titration curve of a polyprotic acid shows
an equivalence point for the each protonation:
Figure %: Titration curve of a strong base titrating a polyprotic acid
The titration curve shown above is for a diprotic acid such as
H2SO4 and is not unlike two stacked . For a diprotic acid, there are two
buffering regions and two
equivalence points. This proves the earlier assertion that
polyprotic acids lose their
protons in a stepwise manner.