Testing for Organic Functional Groups (Oxford AQA International A Level Chemistry)
Revision Note
Written by: Richard Boole
Reviewed by: Stewart Hird
Required Practical 5: Functional Group Testing
Objective
To test for the alcohol, aldehyde, alkene, carboxylic acid and halogenoalkane functional groups
Apparatus
Ethanol
Small pieces of metallic sodium under petroleum ether
A beaker of ethanol should be available for the safe disposal of any excess sodium
Ethanal / propanal
Fehling’s A and B solutions
Cyclohexene
Bromine water
Solid sodium hydrogencarbonate
Dilute ethanoic acid
1-bromobutane
Sodium hydroxide solution
Dilute nitric acid
Silver nitrate solution (0.05 mol dm–3)
250 cm3 beaker
Anti-bumping granules
Test tubes, boiling tubes and a test-tube holder
Thermometer (–10 °C to 110 °C)
Pipettes
Method
The required practical involves five separate experiments
The results from each experiment should be presented in an appropriate table
Part 1 – Testing for an alcohol
Place 1 cm3 of ethanol in a dry test tube
Add a small piece of metallic sodium
Record your observations
Safely dispose of any excess sodium using the beaker of ethanol provided
Part 2 – Testing for an aldehyde
Place 1 cm3 of sodium carbonate solution in a test tube
Add some anti-bumping granules
Mix equal volumes of Fehling's A and Fehling's B into a clean test tube
The resulting Fehling's solution should be a clear dark blue colour
Add 5 drops of the Fehling's solution to the sodium carbonate test tube
Add 1 cm3 of ethanal (or propanal) to this same test tube
Warm the test tube gently for approximately 5 minutes in a water bath
Remove the test tube and allow its to stand for several minutes
Record your observations
Part 3 – Testing for an alkene
Place 2 - 3 drops of cyclohexene in a test tube
Add 1 cm3 of bromine water
Shake the contents of the tube vigorously
Record your observations
Part 4 – Testing for a carboxylic acid
Place one small spatula of solid sodium hydrogencarbonate in a boiling tube
Add 2 cm3 of dilute ethanoic acid
Record your observations
Part 5 – Testing for a halogenoalkane
Place 1 cm3 of sodium hydroxide solution in a test tube
Add 5 drops of 1-bromobutane
Warm the contents of the test tube for a few minutes in a water bath at ~60 °C
Add 2 cm3 of dilute nitric acid to acidify the contents of the test tube
Add 1 cm3 of silver nitrate solution
Record your observations
Practical Tip
The volumes of chemicals do not need to be precise for these experiments because you are looking for a general observation
Results
Chemical | Test | Result |
---|---|---|
Ethanol | Sodium | |
Ethanal | Fehling's solution | |
Cyclohexene | Bromine water | |
Ethanoic acid | Sodium hydrogencarbonate | |
1-bromobutane | Acidified silver nitrate |
Evaluation
Once you have recorded the results from the tests, use them to check that the functional group has given the correct result
Worked Example
Compounds A - E are known to be an alcohol, an aldehyde, an alkene, a carboxylic acid and a halogenoalkane.
The following tests were carried out on organic compounds A - E and the results recorded below:
Test | A | B | C | D | E |
---|---|---|---|---|---|
Acidified AgNO3 (aq) | - | Yellow precipitate | - | - | - |
Br2 (aq) | Decolourises | - | - | - | - |
Fehling's solution | - | - | - | Blue solution to red precipitate | - |
Na (s) | - | - | - | - | Fizzing |
NaHCO3 (s) | - | - | Fizzing | - | - |
Identify each type of organic compound.
Answer:
Compound A: Alkene
Bromine water turns from orange-brown to colourless in the the presence of carbon-carbon double bonds / alkenes
Compound B: Iodoalkane (halogenoalkane)
Silver nitrate, AgNO3, is the test for halogenoalkanes
Iodoalkanes form a yellow precipitate
Compound C: Carboxylic acid
Sodium hydrogencarbonate reacts with carboxylic acids to release bubbles of carbon dioxide gas
Compound D: Aldehyde
Fehling's solution changes from a blue solution to a (brick-)red precipitate in the presence of aldehydes
Compound E: Alcohol
Sodium reacts with alcohols to release bubbles of hydrogen gas
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