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Introduction
One of the solution involved in a titration is used as standard solution. The standard solution can
be as classified as either primary or secondary. A primary standard solution is prepared by
dissolving an accurately weighed pure solid of a known molar mass in a known molar mass in a
known volume of distilled water.
A primary standard is used to determine the morality of the other standard solution, known as
secondary standard. For example, oxalic acid,H2C2, and potassium hydrogen phthalate, KHC8H4O4
are two common primary standards used to determine the concentration of bases (secondary
standard).
Solutions of NaOH and HCl used in titrations need to be standardised because they contain
impurities. Solid NaOH is hygroscopic (it absorbs moisture). Thus, it is difficult to obtain its
accurate mass. The standardised base can then be used to determine the determine the
concentrations of other acids.
An equivalence point is the point at which exact reaction occurs between the two reagents
according to stoichiometry. To detect this equivalence point, an indicator which produces a
change in colour is often used. The point at which the indicator changes colour is called the end
point. The end point and equivalence point should ideally be the same.
Chemical equation
Burrette
Glass rod
White tile
Retort stand
Filter funnel
Beaker (50ml)
Pipette (25ml)
Analytical balance
Chemical Reagents
x M HCl
0.2M NaOH
Distilled water
Phenolphthalein
Procedure
1. Weigh to the nearest 0.0001g about 3.25g of hydrated oxalic acid, H2C2O4.2H2O in a 50mL
beaker.
3. Transfer the solution into a 250mL volumetric flask. Rinse the beaker and pour the content
into the flask. Add distilled water up to the callibated mark of the volumetric flask.
2. Fill the burette with the NaOH solution. Ensure there are no air bubbles trapped at the tip.
4. Pipette 25mL of oxalic acid solution form Part (A) into a 250mL conical flask. Add 2 drops of
phenolphthalein to the oxalic acid solution.
5. Place a white tile unerneath the flask so that any colour change can be clearly observed.
6. Titrate the acid with the acid NaOH solution from the burette. During the titration,swirl the flask
continuosly.
7. Rinse the unreacted solutions at the inner wall of the conical flask with distilled water.
8. Upon reaching the end point, a temporary pink solution appears but fades when the solution is
swirled. Continue titrating until a pale pin colour persists for more than 30 seconds.
(0.025) MA = 0.0357
MA = 1.428M