A titration is a method of analysis that will allow you to determine the precise endpoint of a reaction and therefore the precise quantity of reactant in the titration flask. A buret is used to deliver the second reactant to the flask and an indicator or pH Meter is used to detect the endpoint of the reaction.
Doing a Titration
Begin by preparing your buret, as described on the buret page. Your buret should be conditioned and filled with titrant solution. You should check for air bubbles and leaks, before proceding with the titration.
Take an initial volume reading and record it in your notebook. Before beginning a titration, you should always calculate the expected endpoint volume.
Prepare the solution to be analyzed by placing it in a clean Erlenmeyer flask or beaker. If your sample is a solid, make sure it is completely dissoloved. Put a magnetic stirrer in the flask and add indicator.
Use the buret to deliver a stream of titrant to within a couple of mL of your expected endpoint. You will see the indicator change color when the titrant hits the solution in the flask, but the color change disappears upon stirring.
Approach the endpoint more slowly and watch the color of your flask carefully. Use a wash bottle to rinse the sides of the flask and the tip of the buret, to be sure all titrant is mixed in the flask.
As you approach the endpoint, you may need to add a partial drop of titrant. You can do this with a rapid spin of a teflon stopcock or by partially opening the stopcock and rinsing the partial drop into the flask with a wash bottle. Ask your TA to demonstrate these techniques for you, in the lab.
Make sure you know what the endpoint should look like. For phenolphthalein, the endpoint is the first permanent pale pink. The pale pink fades in 10 to 20 minutes.
If you think you might have reached the endpoint, you can record the volume reading and add another partial drop. Sometimes it is easier to tell when you have gone past the endpoint.
When you have reached the endpoint, read the final volume in the buret and record it in your notebook.
Subtract the initial volume to determine the amount of titrant delivered. Use this, the concentration of the titrant, and the stoichiometry of the titration reaction to calculate the number of moles of reactant in your analyte solution.
Titrating with a pH meter
Titration with a pH meter follows the same procedure as a titration with an indicator, except that the endpoint is detected by a rapid change in pH, rather than the color change of an indicator.
Arrange the sample, stirrer, buret, and pH meter electrode so that you can read the pH and operate the buret with ease.
To detect the endpoint accurately, record pH vs. volume of titrant added and plot the titration curve as you titrate.
2006-11-26 19:14:56
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answer #1
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answered by DemoDicky 6
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You need to use a pH-meter.
You add stepwise base as a titrant to a solution of the compound and measure the pH-value.
Do the plot pH vs volume of base added.
From the plot determine the coordinates of the equivalence point.
Take the volume of added base that corresponds to the equivalence point and divide it by 2. Then find on your plot the value of pH for that volume (1/2*Vequivalence point).
That pH value is equal to the pKa.
You can also check my answer to a similiar question at http://answers.yahoo.com/question/index;_ylt=AtBnp7p9n5Ne0g2nXkqtEVzsy6IX?qid=20061114185658AAkjYTq
and at the links I provide there you can see more details.
2006-11-27 06:21:32
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answer #2
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answered by bellerophon 6
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If i'm not wrong,
Gotta form ionic equation for the reaction. Compute the concentration of H+ and sub the value into this equ -log [H+] = pKa
2006-11-27 10:14:07
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answer #3
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answered by Failure 2
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Refer to this question for the answer:
http://answers.yahoo.com/question/index;_ylt=Ahe4P24YKMCwhRiiOibGdtvzy6IX?qid=20061126235844AAXhMV2
2006-11-27 03:04:27
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answer #4
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answered by jacinablackbox 4
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