CHM 420 Laboratory Report Experiment 7
CHM 420 Laboratory Report Experiment 7
Objective
Introduction
Procedure
Dried sodium oxalate, Na2C2O4 was weighed accurately between 0.2 to 0.25 g
into a conical flask. 40 mL of 1M sulfuric acid solution was added. The solution
was heated gently to 60°C and without delay, the solution was titrated with
permanganate solution until the first persistent pink colour. Temperature was
maintained at 55-57°C. The titration was repeated to obtain 2 acceptable results
and the data was recorded in Table 7.1.
2. Analysis of Ore
Data
Table 7.1
Trial 1 Trial 2
Table 7.2
Calculations
Ionic equations
Average weight of Na 2C 2 O 4 =
(0.2352 + 0.2140 )g
2
= 0.2246g
0.2246g
Mol of Na 2 C 2 O 4 =
134 gmol −1
= 1.68 10 -3 mol
Ionic equations
(
Mol of MnO 4 = (0.09M ) 3 10 −4 L
−
)
= 2.7 10 −5 mol
25mL 1
Scale of titrated = =
100mL 4
(
Total mass of iron(II) in original sample = 4 7.54 10 −3 g )
= 0.0377g
0.0377g
% of iron = 100%
0.2797g
= 13.48%
Questions
Average weight of Na 2C 2 O 4 =
(0.2352 + 0.2140 )g
2
= 0.2246g
0.0377 g
Concentration of iron(II) =
0.025 L
= 1.508 gL−1
(
Total mass of iron(II) in original sample = 4 7.54 10 −3 g )
= 0.0377g
0.0377g
% of iron = 100%
0.2797g
= 13.48%
The end point that the titration reach indicates that the solution was completely
oxidized. The solution will turns from colourless to permanent colour change
which is faint pale pink. The colour changing is due to the presence of KMnO 4.
There is no more solution left to oxidize it. Hence, KMnO4 acts as self-indicator.
3. Typically, a solid iron ore is dried in an oven before analysis. How would the
percentage of Fe determined be affected if the ore had not been dried ?
It would have a higher mass due to the extra moisture and so the percentage of
iron would be smaller.
From equations, MnO4– is reduced to Mn2+ and C2O4– is oxidised to CO2 . The
oxidation number of carbon in C2O4– changes from +3 to +4. In this case, colour of
standard solution is changed because its reduction by sodium oxalate. After the
standard solution was completely oxidized, the appearance of a faint pale pink colour
produced by the addition of a little excess of unreacted potassium permanganate show
that the end point has been reached. Moreover, temperature of sodium oxalate along
with H2SO4 need to be maintained at 55-57°C . This is because the reaction takes
place at higher temperature. During the titration, first manganous sulphate is produced
and acts as a catalyst for the reduction of KMnO4 by sodium oxalate. Thus, reaction
rate in the beginning is slow and the rate of the reaction increases as the reaction
proceeds.
2. Analysis of Ore
To prepare standard solution, iron ore was put into the conical flask and then 30
mL distilled water and 30 mL of 1M sulfuric acid were added into the conical flask.
The mixture was heated on hot plate to dissolves the ore. The mixture was filtered
into a 100 mL volumetric flask and the mark was filled up with sulfuric acid. Only 25
mL was pippeted from volumetric flask into conical flask to be titrated with KMnO 4.
These volumes is used to calculate scale of titration to find mass of iron(II) in original
sample.
From overall experiment, the presence of sulfuric acid is to supply the proton H+
and then preventing the formation of a manganese(IV) oxide precipitate. Formation
of MnO2 which would not give a good end point and causing errors and quantitative
complications. Diluted sulphuric acid also does not undergo any redox reactions under
the conditions of this titration. Potassium permanganate acts as a self-indicator in this
titration.
There are some precautions that must been followed in order to get accurate result.
The air gaps must be removed from the burette and never forget to remove the funnel
from the burette before noting the initial reading of the burette to get accurate reading
of burette.
Conclusion
References
Neil D. Jespersen & Alison Hyslop. (2014). Chemistry: The Molecular Nature of
Matter, 7th Edition. John Wiley and Sons, Incorporated.