IB1 Chemistry Practical #8 ANALYSIS OF ASPIRIN TABLETS For a long time the bark of the willow tree (salix alba) was used as a traditional medicine to relieve the fever symptoms of malaria. In the 1860's chemists showed that the active ingredient in willow bark is salicylic acid (2-hydroxybenzoic acid) and by 1870 salicylic acid was in wide use as a pain killer (analgesic) and fever depressant (antipyretic). However, because it is a relatively strong acid, salicylic acid has the undesirable side effect of irritating and damaging the mouth, esophagus and stomach membranes. In 1899 the Bayer Company of Germany introduced the ethanoate ester of salicylic acid, naming it 'Aspirin'. Since that time mild analgesics containing aspirin have appeared under many different brand names. The aim of this experiment is to determine the percentage of aspirin present in different commercial preparations and to find which is the best value for money. The analysis makes use of the fact that aspirin is a monoprotic (monobasic) acid and therefore reacts with sodium hydroxide according to the equation:
C6H5(OCOCH3)COOH + NaOH
C6H5(OCOCH3)COONa+ + H2O
ENVIRONMENTAL CARE: None of the reactants or products are particularly harmful to the environment and the waste can be safely disposed of down the sink. SAFETY: No special precautions are necessary. You might like to consider why many doctors now recommend that you take paracetamol rather than aspirin for a headache even though aspirin is an effective mild analgesic. ASSESSMENT: This practical may be formally assessed for Data Collection & Processing and Conclusion & Evaluation.
PROCEDURE. Note the brand name and the price of the aspirin tablets you are using. Weigh out accurately one tablet (about 0.4 - 0.5g) into a 50 cm3 conical flask and dissolve it in 10 cm3 of 95% ethanol. Titrate with 0.10 mol dm-3 sodium hydroxide solution using two drops of phenolphthalein solution as an indicator.
CALCULATIONS. 1. How many moles...