AP Chemistry - Acid-Base Titration Lab
AP Chemistry - Acid-Base Titration Lab
AP Chemistry - Acid-Base Titration Lab
The purpose of this lab is to determine the molar mass of solid tartaric acid. To do
this, a solution of sodium hydroxide will first be standardized against a weighed sample of
potassium hydrogen phthalate (KHP), an acid whose mass and composition is consistent
over time. The sodium hydroxide will then be used to titrate a solution of tartaric acid so
that the molar mass of tartaric acid can be accurately calculated.
Background:
An acid/base titration is performed by carefully adding one solution from a buret, the
titrant, to another substance in a flask until all of the substance in the flask has reacted. To
show when the titration is complete, a dye called an indicator is added to the solution to show
when the end point, or the color change indicated when chemical equilibrium between moles
of the acid and moles of the base is reached. In the titration performed in this experiment, the
reactant NaOH must be standardized against a primary standard such as KHP because it is a
compound that changes chemical composition in storage. Solid NaOH absorbs water vapor so
that the mass of pellets of NaOH is partly NaOH and partly water. Thus, it is impossible to
know the exact molarity of any solution of NaOH without standardizing it by titration because
of the variable water content that will distort and invalidate a mass measurement. A heat-dried
sample of KHP can be relied on to be 100% KHP; thus, an accurately determined mass of
KHP will reveal an accurate number of moles of sodium hydroxide.
Materials
Potassium hydrogen phthalate 250ml Erlenmeyer flask
(KHP), 204. g/mol Graduated cylinder
NaOH solution (approx. 0.100M) Distilled water bottle
Tartaric acid Analytical balance
Phenolphthalein (Phth) indicator Magnetic stirrers
Buret and clamp Bottle container
Procedure:
Part 1: NaOH and KHP
1) Obtain a clean buret washed with soap and rinsed with distilled water.
2) Calculate mass of NaOH in a 0.1M solution of NaOH, and obtain the calculated mass
using weigh boats. Be sure to “tare” the balance with only the weigh boat on it before
adding the NaOH.
3) Put massed NaOH in a Florence flask, and add water to the 1L mark.
4) Place a magnet into the flask, and the flask on the stirrer. Turn on the stirrer and
dissolve the NaOH.
5) Pour the solution into a bottle container.
6) Measure out 0.5g-1.0g of KHP, and record the exact mass. Put the KHP in an
Erlenmeyer flask, add about 100mL of distilled water, and dissolve it using the
magnet stirrers.
7) Add 2-3 drops of Phenolphthalein indicator into the Erlenmeyer flask.
8) Rinse the buret with a small portion of the NaOH solution. Clamp it so that the buret
will drip into the Erlenmeyer flask. Then, using a funnel, fill the buret with the
solution to the “0” mark, making sure not to let solution spill over the top.
9) Calculate the amount of NaOH theoretically needed to reach the equivalence point,
and add 10mL less than that from the buret to the flask.
10) Open the buret slightly so that NaOH will drip slowly.
11) When the color of the solution in the flask turns slightly pink, tighten the buret,
calculate the amount of NaOH used, and record the data.
12) Calculate the molarity and label bottle container containing NaOH solution.
13) Repeat titration twice.
Conclusion:
The molar mass of solid tartaric acid is 150.0g/mol. This mass was found by first
multiplying the volume of NaOH required to reach the end point (avg. of trials was
21.34mL) and the molarity of the NaOH solution (calculated by dividing moles of KHP
by volume of NaOH needed to complete the titration) to calculate moles of NaOH
(0.0974M). Since the molar ratio of tartaric acid to NaOH is 1:2, dividing the calculated
moles of NaOH by 2 yielded the moles of tartaric acid in the sample (avg. of trials was
0.00104). Lastly, dividing the measured mass of tartaric acid (0.155g) by the calculated
moles of acid yielded the molar mass of tartaric acid. The average of the three trials
showed the molar mass of tartaric acid to be 150.0g/mol. The calculations used in this
experiment largely relied on stoichiometry and the definition of molarity (moles divided
by liters) to allow the manipulation of data for the desired information – molar mass of
tartaric acid. The chemical process that occurred during the titration of NaOH and tartaric
acid involved hydroxide (OH-) ions reacting with the hydrogen (H+) ions floating in the
solution of dissolved H2C4H4O6 in the beaker. So, for every mole of acid 2 moles of
hydrogen ions reacted with the hydroxide ions dissolved in the solution, as tartaric acid is
a diprotic acid. When the equivalence point was reached, signifying chemical equilibrium
between moles of H2C4H4O6 acid and moles of the NaOH base, the end point, or the pink
color change, indicated that the titration was complete.