Experiment date: 2013/10/29
- Principle:
We’ll learn how to use lodine to titration the Vitamin C in juice or Vitamin C
tables. And find out the damage level from air or temperature at the same time. We can also learn the meaning and the way to use acid-base back titration.
- Chemicals and their Properties:
H2SO4 (CAS 7758-01-2): 167.0005 g/mol d:1.84g/cm3 mp: 10 °C
bp: 337 °C
KBrO3 (CAS 7664-93-9): 148.1 g/mol d: 3.27 g/cm3 mp: 350 °C dp: 370 °C Looks: White powder
Na2S2O3 (CAS 7772-98-7): 158.09774 g/mol d:1.84g/cm3 mp: 48.3 °C
KBr (CAS 7758-02-3): 119.0023 g/mol d: 2.75g/cm3 mp: 734 °C
bp: 1435 °C
KI (CAS 7681-11-0): 166.0028 g/mol d: 3.123 g/cm3 mp: 681 °C bp: 1330 °C
Starch iodide (CAS 9005-25-8): d: 1.5 g/cm3 Looks: White powder
Vitamin C (CAS 50-81-7): d: 1.694g/cm3 mp: 190–192 °C bp: 553 °C
- Tools:
1. Pasteur pipette (10mL)
2. Erlenmeyer flasks (125mL)
3. Mortar and pestle
4. Volumetric flask(50mL)
5. Filter paper
6. Burettes
- Safety and Waste Disposal:
Safety : Always wear your coat, gloves and eye protection.
- Procedure:
Part. A (Vitamin C tables)
- Take a table of Vitamin C, and find its weight.
- Use the mortar and pestle to make it into powder.
- Quickly use KBrO3 to titration it until it become a little bet yellow. Write down its weight.
- Add 0.5g KI, and add 5mL starch with water after KI is totally dissolute. Then use Na2S2O3 to titration it until it is not looking blue. Write down the amount of Na2S2O3 that had been used.
- Calculate the amount of each of the Vitamin C table.
Part. B (Juice)
- Filter about 100mL of juice.
- Put 20mL of juice from step one to a 50mL volumetric flask. Then add 0.5g KBr and fill the volumetric flask with 1M H2SO4. Put it in a Erlenmeyer flask, and then start to titration as fast as possible. Write down the Vitamin C in the juice.
- Take another 20mL juice and put in another Erlenmeyer flasks and put in hot water with a stopper for 20 minutes. After it cold down, Put it in a volumetric flask. Add 0.5g KBr and fill the volumetric flask with 1M H2SO4. Put it in a Erlenmeyer flask, and then start to titration as fast as possible. Write down the Vitamin C in which is destroyed because of heat.
- Take another 20mL juice and put in another Erlenmeyer flasks and stir hard in the air for 20 minutes. Put it in a volumetric flask. Then add 0.5g KBr and fill the volumetric flask with 1M H2SO4. Put it in a Erlenmeyer flask, and then start to titration as fast as possible. Write down the Vitamin C in which is destroyed because of the reaction with air.
- Results:
First |
second |
third |
|||
Na2S2O3 |
KBrO3 |
Na2S2O3 |
KBrO3 |
Na2S2O3 |
KBrO3 |
44.8mL |
10.49mL |
81.2mL |
17.1mL |
59.7mL |
13.3mL |
0.00245mole |
0.00052mole |
0.00444mole |
0.00085mole |
0.00327mole |
0.00066mole |
I2 |
Br2(Total) |
I2 |
Br2(Total) |
I2 |
Br2(Total) |
0.00123mole |
0.00157mole |
0.00222mole |
0.00256mole |
0.00163mole |
0.00199mole |
Br2(titration with I-) |
Br2(reaction with Vitamin C) |
Br2(titration with I-) |
Br2(reaction with Vitamin C) |
Br2(titration with I-) |
Br2(reaction with Vitamin C) |
0.00123mole |
0.00034 mole |
0.0222e |
0.00034 mole |
0.00163mole |
0.00036 mole |
Vitamin C |
Vitamin C (g) |
Vitamin C |
Vitamin C (g) |
Vitamin C |
Vitamin C (g) |
0.00034mole |
0.06123 gram |
0.00034mole |
0.06045 gram |
0.00036mole |
0.06366 gram |
Vitamin C (per table) |
Error rate |
Vitamin C (per table) |
Error rate |
Vitamin C (per table) |
Error rate |
0.31516(g) |
36.97% |
0.30394(g) |
39.21% |
0.31946(g) |
36.11% |
In the situation of |
H2SO4 |
KBrO3 |
|||
0.05917M |
0.049999M |
- Discussion:
It is really hard to control the titration’s speed. We obviously fail 3 times, so we need to restart it. And the second try we just do it as good as possible. This time, we just did it. And the second Erlenmeyer flask’s Vitamin C is a little bit too much, we think it maybe is because we make some accident while we are titration. Because even a little bit more or less, the change is very huge.
- References:
Wikipedia
- Reflection and Feedback:
The second bottle of vitamin C is too big so it could be some kind of error.
And the other two number is close to each other, I think is because the second one we add too little Na2S2O3 so there are not the real data or just others we stop too slow then the last titration is too over.
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