Lab Report 6 CHM138
Lab Report 6 CHM138
CHM 138
(BASIC CHEMISTRY)
INTRODUCTION
Redox reaction involves the transfer of electrons, and an acid-base reaction
involves the transfer of protons. Just as an acid can be titrated against a base,
we can titrate an oxidizing agent against a reducing agent using a similar
procedure. We can carefully add a solution containing an oxidizing agent to a
solution containing a reducing agent. The end point is reached when the
reducing agent is completely oxidized by the oxidizing agent. Two common
oxidizing agents are potassium dichromate (K2Cr 2O7) and potassium
permanganate (KMnO4). The colours of the dichromate and permanganate
anions are distinctly different from those of the reduced species.
Cr2O72- → Cr3+
Yellow-orange Green
MnO4- → Mn2+
Light purple Pink
Thus these oxidizing agents can themselves be used as an indicator in a redox
titration because they have distinctly different colours in the oxidized and
reduced forms. Redox s titration requires the same type of calculations (based
on the mole method) as acid-base neutralizations.
In this experiment, KMnO4 solution of known concentration will react with an
acidified solution of FeSO4 of unknown concentration. This reaction involves
oxidation and reduction reactions (redox) in which electrons are transferred
from one substance to another. In this redox reaction, Fe2+ is converted into Fe3+
and MnO4- is converted into Mn2+. The change in the oxidation state of
manganese in MnO4- to Mn2+ causes a change in colour. When the reaction is
complete, and excess MnO4- is added to the reaction mixture, the solution turns
pink and the titration is done.
PROCEDURE
1. Burette was washed with distilled water and then rinsed with about 5-10
mL of KMnO4 solution, the second rinsing runned through the burette tip.
The burette clamped to the retort stand.
2. The burette filled with KMnO4 solution. Make sure the tip is completely
filled and contain no air bubbles. The initial burette reading recorded to
two decimal places. Since the colour of the KMnO4 solution is quite
intense, you may be required to give a good estimate of the burette
volume.
3. On an analytical balance, 8 g FeSO4 weighed accurately using weighing
paper. The mass of FeSO4 recorded.
4. With the aid of a filter funnel, the FeSO4 transferred carefully to a 250 mL
volumetric flask. The filter funnel rinsed with distilled water into the
volumetric flask. Using a graduated cylinder, 10 mL of 2 M sulphuric
acid added into the volumetric flask. Distilled water added until the
calibration mark (use a dropper to add the last few drops of distilled
water). The volumetric flask shaked by turning it upside-down a few
times in order for the solution to be homogeneous.
5. About 50 mL of FeSO4 solution poured into a small beaker. 20 mL
pipette washed with distilled water and rinsed with FeSO4 solution (all
rinsing solutions must be discarded). 20 mL of FeSO4 solution pipette
into a 250 mL conical flask (ensure there no air bubbles at the tip of the
pipette)
6. 10 mL of 2 M sulphuric acid added into the conical flask by using a
graduated cylinder.
7. Conical flask was placed on a piece of white paper or white tile (DO
NOT USE FILTER PAPER) under the burette and the burette tip lowered
into the conical flask.
8. The titration apparatus was setup. This solution titrated with the standard
KMnO4 from the burette until the end point reached. During the titration,
the conical flask kept swirling. The end point is indicated when the
solution turns to a LIGHT PINK permanently. The final burette reading
recorded. This is the result of the ROUGH TITRATION.
9. The titration process repeated until two consecutive titrations (meaning,
one titration after another) agree to +/- 0.10 mL .
RESULT
DATA
NUMBER TITRATION TITRATION TITRATION TITRATION
OF 1 2 3 4
TITRATION
Final burette 5 10 15 18
reading (mL)
Initial burette 0 5 10 15
reading (mL)
Volume of 5 5 5 3
KMnO4 used
(mL)
Mass of FeSO4 used = 8 g
CALCULATIONS
Half reaction
Balance
Fe2+ → Fe3+ + e
MnO4- + 8H + 5e → Mn2+ + 4H2O
DISCUSSION
i. The result that we got are same with the theory said. Reduction of purple
permanganate ion to the colourless Mn+2 ion, the solution will turn from
dark purple to a faint pink colour at the equivalence point
ii. The initial and final readings of the burette is recorded and repeated three
times includes rough titration. The final burette reading of the titration
are fixed to all the titration. So, the result that we got in this experiment
are accurate.
CONCLUSION
From this redox titration lab, we were able to determine the unknown molarity
of a substance that went through a redox chemical reaction. For our lab, the
concentration of th solution was determined to be 1.052 Molar. According to the
listed concentration of the Fe2+ solution, which was given to one significant
figure at 1 M, our answer at one significant figure had 0% error. This answer
reflects the precision of the given unknown solution, not our measured
precision, as the tools we used to measure our experimental value were more
precise. As a result, the unknown molarity of the Fe2+ solution was determined
in this lab through the use of a redox titration.
QUESTION
1. Why did the solution turn to light pink at the end of the titration?
OXIDATION REDUCTION
All the above reactions releases All the above reactions store
energy energy
REFERENCE
• http://www.majordifferences.com/2016/04/difference-between-oxidation-
and-reduction.html#.WK9rUlV97IU
• https://sites.google.com/a/student.roundrockisd.org/redox-titration-
lab/data-and-calculations-from-the-lab/lab-s-conclusions
• https://answers.yahoo.com/question/index?qid=20080913201743AAQ6
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