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Procedure
a.
Weigh accurately a definite number of aspirin tablets (two or three tablets weighing no
more than 1.5 g) into a 250 cm3 conical flask. Initiate the hydrolysis of the aspirin by
adding 25 cm3 of 1.0 M sodium hydroxide by pipette, diluting with approximately the
same volume of distilled water. Warm the flask over a tripod and gauze for ten minutes to
complete the hydrolysis.
b.
Cool the reaction mixture and transfer with washings to a 250 cm3 volumetric flask, dilute
to the mark with distilled water and then ensure that the contents of the flask are well
mixed by repeated shakings.
c.
Titrate 25 cm3 portions of the diluted reaction mixture with the standard 0.050 M
sulphuric acid provided, using phenol red indicator until two or three consistent results are
obtained.
d.
Calculate the weight of acetylsalicylic acid in each tablet and compare your results with
the manufacturer's specification. Compare your results with those given in different brands
of aspirin.
Titration Results
Titration
trial
Explain why it is necessary to warm the reaction mixture of aspirin and sodium hydroxide
solution.
It is to ensure that the alkaline hydrolysis is complete.
2.
Explain why phenol red (or phenolphthalein) is used as the indicator in this experiment.
After the hydrolysis of aspirin, the two salts formed are alkaline. Hence, an indicator with
an alkaline pH range (6.8-8.4) is suitable for the titration.
P.2
14.56
= 7.28 10-4
1000
Na2SO4 + 2H2O
No. of moles of excess NaOH (25 cm3, in conical flask) = 2 7.28 10-4 = 1.45610-3
No. of moles of excess NaOH in the volumetric flask (250cm3) = 1.45610-3 10 = 1.45610-2
No. of moles of NaOH in the original solution (procedure a) = 1.027
25
1000
= 0.02568
No. of mole of NaOH reacted with aspirin = 0.02568 0.01456
= 0.01112
CH3COOC6H4COOH(s) + 2NaOH(aq)
0.01112
= 0.00556
2
1.0008
= 0.3336 (g)
3
1.0008
100%
1.092
= 91.65 %
P.3