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Weak Acid Titration v
You are encouraged to carefully read the following sections in Tro (3rd^ ed.) to prepare for this experiment: Sec 4.8, pp 168-174 (Acid/Base Titrations), Sec 16.4, pp 769-783 (Titrations and pH Curves).
Objectives: You will be able to: (1) determine the hydrogen ion concentration of a weak acid via titration against a strong base, (2) calculate the pH of a weak acid / strong base titration at the endpoint of a titration, (3) evaluate a pH titration curve and determine the pH of a weak acid / strong base titration at the equivalence point, (4) use the molar solubility, as determined from the hydrogen ion concentration, to determine the Ksp of an ionic compound.
Background: In an acid-base titration, a solution of unknown concentration is reacted with a standard solution of known concentration. The progress of the reaction is monitored using a pH meter or an indicator. When an indicator is used, the titration continues until the indicator changes color to signal the endpoint of the titration. The endpoint occurs in the first drops past the equivalence point. The equivalence point is the point at which the number of moles of base is stoichiometrically equivalent to the number of moles of acid.
To see how this data can be used, follow the titration of hydrofluoric acid against sodium hydroxide:
HF (aq) + NaOH (aq) H 2 O (l) + NaF (aq)
If 35 mL of HF required 25 mL of 0.250 M NaOH to reach the pink phenolphthalein endpoint, what is the concentration of HF? At this point, simply determine the concentration of the HF stoichiometrically.
[HF] = 0.0250 L NaOH x 0.250 mol NaOH x 1 mol HF x 1 = 0.179 M HF 1 L NaOH 1 mol NaOH 0.0350 L HF
Note that 0.179 M HF is equal to the concentration of the weak acid at the start of the titration. To determine the pH at the start of the titration, we will use this information, the Ka of HF, an ICE table for the dissociation of HF in water, and pH = -log [H 3 O+]
HF (aq) + H 2 O ( l ) H 3 O+^ (aq) + F-^ (aq) Ka = 3.5 x 10-
HF H 3 O+^ F- Initial Conc. 0.179 0 0 Change in Conc. - x + x + x Equilibrium Conc. 0.179 - x X x
3.5x10-4^ = Ka =
[H 3 O+][F−]
[HF]
(x)(x) 0.179−x
Now solve for x using the quadratic equation and you get x = [H 3 O+] = 0.00774 M. Plugging that into the pH equation, you find the initial pH of the solution is 2.11.
At the equivalence point (endpoint in this experiment since the initial concentration of acid was determined experimentally from the endpoint) all of the weak acid will have reacted with the strong base to form the conjugate weak base as can be seen in the table below. The concentrations of the weak acid and the strong base that react are:
[HF] = (0.179 M HF)(0.0350 L) / (0.0600 L) = 0.104 M HF [OH-] = (0.250 M OH-)(0.0250 L) / (0.0600 L) = 0.104 M OH- Note: You must take into account the dilution from the presence of both solutions.
HF (aq) + OH-^ (aq) H 2 O (aq) + F-^ (aq)
HF OH-^ F- Before reaction 0.104 0.104 0 reaction changes -0.104 -0.104 +0. After reaction 0 0 0.
So, the reaction that determines the pH of the solution at the equivalence point is actually the interaction of the product weak base in water. An ICE table can be used to figure out the concentrations of the reactants and products at equilibrium.
F-^ (aq) + H 2 O (l) OH-^ (aq) + HF (aq) Kb = 2.9 x 10-
F-^ HF OH-
Initial Conc. 0.104 0 0 Change in Conc. - x + x + x Equilibrium Conc. 0.104- x (^) x x
2.9x10-11^ = Kb =
[OH−][HF]
[F−]
(x)(x) 0.104−x
Solve for x using the quadratic equation and you get x = [OH-] = 1.7 x 10-6^ M. Plugging that into the equation pOH = -log [OH-], you find the pOH of the solution is 5.77. Finally, using the equation 14.00 = pH + pOH, you find that the pH = 8.23.
Titration of a Saturated Potassium Hydrogen Tartrate (KHT) Solution Against Standardized NaOH
Preparation of the Saturated KHT Solution for Titration
- Gather: a. 2 125-mL Erlenmeyer flasks (washed and rinsed with and distilled water) b. 1 400-mL beaker (washed and rinsed with distilled water) c. 1 funnel (washed and dried) d. 1 25-mL volumetric pipet (washed) e. Pipet filling pump f. Stirring rod (washed and dried) g. 1 piece of filter paper h. 1 250-mL Erlenmeyer flask (washed and dried)
- Weigh 2.8 g of KHT.
- Transfer the KHT into a clean 400-ml beaker.
- Add distilled water to the KHT in the beaker until the level reaches the 200 mL mark on the beaker.
- Stir the solution with a stir rod for approximately 10 min to ensure saturation.
- Filter your mixture into the 250 mL Erlenmeyer flask (note: the filtrate that passes through the filter must be clear).
- Rinse a 25-mL volumetric pipet once with a small portion of your clear filtrate, drawing some of the filtrate into the volumetric pipet to rinse the pipet as well. Discard the rinse down the drain.
- Using the volumetric pipet, transfer 25 mL of the saturated KHT solution into a 125-mL Erlenmeyer flask and record on the data sheet as volume of KHT solution to the nearest 0.01 mL.
- Repeat one more time into the additional 125-mL flask and then a final sample into the 250 mL beaker (for use later during the pH titration).
- Add two drops of phenolphthalein indicator to each of the saturated KHT solutions in the 125-mL Erlenmeyer flasks.
Preparation of the Standard NaOH Solution for Titration Remember standardized NaOH is valuable and time consuming to make. Take only what you need from the bottle, and be certain the stock bottle is tightly sealed after you use it.
- Rinse the buret with a small portion (~5 mL) of the NaOH solution, discard this rinse.
- Fill the buret with NaOH and make sure that the tip of the buret is filled with NaOH solution by opening the stopcock. Discard this small amount of solution.
Preparation of the pH meter Be careful never to touch the pH-sensitive circuit of the pH meter with anything but water, aqueous solutions or blotting with a Kimwipe.
- Rinse the sensor of the pH meter with distilled water and blot it dry with a Kimwipe.
- Add pH 7 standard to the sensor.
- Press the calibrate button with the cap off the pH meter.
- Wait until the pH meter stops blinking and reads 7.00. (If this doesn’t happen see your instructor.)
- Rinse the sensor with distilled water and dry with a Kimwipe.
Titration
- Record the indicated molarity of the standardized NaOH solution from the bottle (should be ≈ 0.05 M) onto your data sheet.
- Record the initial buret reading on your data sheet to the nearest 0.01 mL.
- Titrate the solution with the standardized NaOH solution until the light pink end point persists for at least 30 s.
- Record the final buret reading on your data sheet to the nearest 0.01 mL.
- Using a plastic dropper, cover the pH sensor of the pH meter with a drop of your final solution.
- Record the pH in the top portion of your data sheet.
- Rinse the pH sensor with distilled water and blot dry with a Kimwipe.
- Refill your buret with additional NaOH.
- Repeat these steps with the second sample.
pH Curve for the Titration of Saturated Potassium Hydrogen Tartrate (KHT) Solution against Standardized NaOH
pH Curve Titration
- You will use the third 25 mL sample in the 250 mL beaker for this titration.
- Measure the initial pH of the saturated solution by placing the sensor down into the solution. Record the pH on your data sheet for 0 mL of added base. NOTE: Be certain to prevent the beaker from tipping over.
- Rinse the sensor with distilled water and blot dry with a Kimwipe.
- Add 1 mL NaOH to the beaker mixture. Swirl the contents to ensure complete reaction.
- Again measure the pH of this new mixture by setting the sensor back into the reaction mixture.
- Record the pH and total volume of NaOH added on your data sheet.
- Repeat the steps of adding NaOH and measuring the pH until you have added 20 mL of NaOH to your KHT solution.
Results and Conclusions
Titration:
- Calculate the molarity of HT-^ from your two best runs. a. Run 1
b. Run 2
- Calculate the average molarity of HT-^ from your two best runs.
- The average molarity of HT-^ equals the acid’s initial concentration. Determine the pH of the solution prior to the titration if the Ka = 4.6 x 10-5^ for HT-.
HT-^ (aq) + H 2 O (l) H 3 O+^ (aq) + T2-^ (aq)
- Calculate the concentration of tartrate (T2-) at the endpoint.
- Calculate the pH of the solution at the endpoint.
T2-^ (aq) + H 2 O (l) OH-^ (aq) + HT-^ (aq) Kb = 2.2 x 10-
- Compare the pH of the endpoint recorded in your data sheet to that calculated in question 5.
- Graph, using Excel, a pH curve for the titration of HT-^ against NaOH. Label the initial pH, buffer region, equivalence point, and excess base regions on your graph.
- What is the pH at the equivalence point according to the titration curve?
- Compare the pH at the equivalence point calculated in question 5 to the pH determined in from the titration curve.
Complete the following table by identifying the one of the four species (HA, A−, H 3 O+, OH−) that is most concentrated, the one that is least concentrated, and any pairs that have nearly equal concentration in the mixture at that point. The first entry is provided for you.
Point on curve
Highest concentration
Lowest concentration
Nearly Equal Concentrations
A HA
B
C
D
- Consider the titration of 20.0 mL 0.120 M HC 2 H 3 O 2 against 0.150 M KOH. a. What is the initial pH of the solution? (HC 2 H 3 O 2 Ka = 1.8 x 10-5)
2
4
6
8
10
12
14
0 10 20 30 40 50
pH
Volume NaOH
A
B
C
D
b. What is the pH after 16 mL (equivalence point) of 0.150 M KOH has been added to the solution. (for C 2 H 3 O 2 - , Kb = 5.6 x 10-10)
