Average Molarity Of Permanganate Solution 2 example essay topic

Purpose: The purpose of this experiment is to determine the molarity of a permanganate solution through the use of red ox titration. Theory: The following are the reactions that take place in the experiment: Unbalanced: H 2 C 2 O 4 (aq) + MnO 4- (aq) CO 2 (g) + Mn 2+ (aq) H 2 C 2 O 4 Half-Reaction: H 2 C 2 O 4 (aq) 2 CO 2 (g) + 2 e- + 2 H+ (aq) MnO 4- Half-Reaction: 8 H+ + 2 MnO 4- (aq) + 5 e- Mn 2+ (aq) + 4 H 20 (l) Net Reaction: 5 H 2 C 2 O 4 (aq) + 6 H+ + 2 MnO 4- (aq) 10 CO 2 (g) + 2 Mn 2+ (aq) +8 H 20 (l) The solution was heated in order to reach better reaction rates, since the reaction occurs slowly at room temperature. Unlike many other titrations no indicator is necessary to tell the experimenter when the endpoint of the reaction is. In this case, the experimenter knows when all the oxalate has been consumed because the excess of permanganate will show up as a pink color. Thus, the permanganate ion acts as an indicator itself.

The reaction produces its own catalyst in the form of Mn 2+ that promotes oxidation. The sulfuric acid added to the titration flask acts as a proton donor for the solution readily giving up protons. Since the oxalic acid is not a strong acid and does not dissociate well, but is still needed in the reaction to form carbon dioxide, the addition of a strong acid, sulfuric acid, supplies the protons needed for the reaction. Procedure: Obtain and zero two bursts, one containing. 0500 M oxalic acid and the other containing the permanganate solution. Next, add 25.00 mL of the oxalic acid into a 250 mL Erlenmeyer flask (using the bottom of the meniscus for measurements).

Then proceed to measure and add 15 mL of 3 M sulfuric acid to the titration flask with a graduated cylinder. Heat the titration flask to a temperature of 80 C. Titrate the contents of the flask with the permanganate solution. Swirl the contents of the flask after adding the permanganate and if the solution drops below 80 C heat the flask back up to 80 C. Use the top of the permanganate solution to take measurements rather than the bottom of the meniscus. Add just enough permanganate to turn the contents of the flask a light pink color. At this point record the volume of the permanganate solution used. Rinse the titration flask with distilled water and run the experiment one more time.

Data: Quantitative: (Trial One): 1. Volume of. 0500 M Oxalic Acid (H 2 C 2 O 4 (aq) ) 25.00 mL 2. Volume of Permanganate Solution (MnO 4- (aq) ) 24.55 mL 3. Volume of Sulfuric Acid (H 2 SO 4 (aq) ) 15.00 mL (Trial Two): 1. Volume of.

Volume of Permanganate Solution (MnO 4- (aq) ) 24.06 mL 3. Volume of Sulfuric Acid (H 2 SO 4 (aq) ) 15.00 mL Qualitative: The sulfuric acid and the oxalic acid are both clear in color, while the permanganate solution is a dark purple color. At first, when the permanganate is added to the titration flask containing both oxalic and sulfuric acid the solution within the flask turns a pink color and suddenly disappears, until the endpoint is reached. The endpoint is when one drop of the permanganate solution changes the color of the titration flask to a slight pink color for more than fifteen seconds. Moles of Permanganate Solution: 2. Liters of Permanganate Solution: 3.

Molarity of Permanganate Solution: (Trial Two): 1. Molarity of Permanganate Solution: (Average of Two Trials): 1. Average Molarity of Permanganate Solution 2. Percent Error Based Upon Class Average Calculation Table (Trial One): 1. Moles of Permanganate Solution. 000500 mol 2.

Liters of Permanganate Solution. 02455 ml 3. Molarity of Permanganate Solution. 0204 M (Trial Two): 1.000500 mol 2.02506 ml 3.0200 M (Average) 1. Average Molarity of Permanganate Solution. 0202 M 2.

Percent Error Based on Class Average 2.42%Results: The molarity of the permanganate solution in the first trial was. 0204 M, while in the second trial the molarity was. 0200 M. The average molarity for the two trials was. 0202 M, which was lower than the class average of.

0207 M. Based upon the class average, the percent error for the molarity was 2.42%. A cause of an error maybe the fact that one does not truly know the ending point of the reaction when all the oxalate is consumed and there is an excess of permanganate. The end is signified by a pinkish tint to the solution, but this tint is often of different intensities and is hard to determine when exactly all the oxalate has been reacted. Another minor source of error may have been during the heating process. Contents of the solution easily stick to the outer layer of the thermometer causing a slight loss of solution. In addition, some contents may have left the flask as vapor during heating.