5 Steps to a 5 AP Chemistry

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Alternate solution:

Titration Equilibria


An acid–base titrationis a laboratory procedure commonly used to determine the concentra-
tion of an unknown solution. A base solution of known concentration is added to an acid
solution of unknown concentration (or vice versa) until an acid–base indicatorvisually
signals that the end pointof the titration has been reached. The equivalence pointis the
point at which a stoichiometric amount of the base has been added to the acid. Both chemists
and chemistry students hope that the equivalence point and the end point are close together.
If the acid being titrated is a weak acid, then there are equilibria which will be established
and accounted for in the calculations. Typically, a plot of pH of the weak acid solution being
titrated versus the volume of the strong base added (the titrant) starts at a low pH and grad-
ually rises until close to the equivalence point, where the curve rises dramatically. After the
equivalence point region, the curve returns to a gradual increase. This is shown in Figure 15.3.
In many cases, one may know the initial concentration of the weak acid, but may be
interested in the pH changes during the titration. To study the changes one can divide the
titration curve into four distinctive areas in which the pH is calculated.

1. Calculating the initial pH of the weak acid solution is accomplished by treating it as a
simple weak acid solution of known concentration and Ka.
2. As base is added, a mixture of weak acid and conjugate base is formed. This is a buffer
solution and can be treated as one in the calculations. Determine the moles of acid con-
sumed from the moles of titrant added—that will be the moles of conjugate base
formed. Then calculate the molar concentration of weak acid and conjugate base, taking
into consideration the volume of titrant added. Finally, apply your buffer equations.
3. At the equivalence point, all the weak acid has been converted to its conjugate base. The
conjugate base will react with water, so treat it as a weak base solution and calculate the
[OH−] using Kb. Finally, calculate the pH of the solution.
4. After the equivalence point, you have primarily the excess strong base that will deter-
mine the pH.

pOH

NH


NH ] 3


=− × +


=+



+
log. log

[]


[


.log

.


181 10


4 742


300


2


(^54)


..


.


00


==4 918 pH 9.082

181 10


300


121 10


14 00


5

5

.


.


.


.


×=



=


=




x

x

2.00


pOH 4.918
pH 0 0 4 918 9 082-.=.

K


xx
b x

4

+

3

NH OH


NH ]


)( )


)


==


+




[][]−


[


(.


(.


.


300


200


181 10−−^5


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