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4.2.4 Required Practical 6 - Organic Tests
Aim
To use chemical tests to identify the presence of different functional groups in organic compounds, including alcohols, aldehydes, alkenes, and carboxylic acids.
Dispose of excess sodium in ethanol to avoid water contact.
Potassium dichromate is a strong oxidizer and toxic:
Use safety goggles, gloves, and a lab coat.
Fehling's solution contains alkalis and copper compounds:
Avoid skin contact and wear protective gear.
Halogenoalkanes are volatile and can be toxic:
Use in a well-ventilated area or fume cupboard.
Nitric acid and silver nitrate are irritants:
Handle with care, wearing gloves and eye protection.
Method
Test for Alcohols
Metal Test:
Add a small piece of metallic sodium to the alcohol in a test tube.
Observe the release of hydrogen gas (test with a lit splint for a "squeaky pop").
Dispose of excess sodium in ethanol.
Potassium Dichromate Test:
Add a few drops of acidified potassium dichromate to the alcohol.
Gently warm and observe the colour change:
Orange to green indicates a primary or secondary alcohol.
No change (remains orange) indicates a tertiary alcohol.
Test for Aldehydes
Fehling's Solution:
Mix equal volumes of Fehling's A and B to prepare the test reagent.
Add 5 drops of the reagent and a few anti-bumping granules to a test tube containing the aldehyde.
Warm gently in a hot water bath and maintain for a few minutes.
A brick-red precipitate confirms the presence of an aldehyde.
Test for Alkenes
Bromine Water:
Add 1 cm³ of bromine water to 2 drops of the suspected alkene.
Shake vigorously.
If the solution decolourises from orange to colourless, an alkene is present.
Test for Carboxylic Acids
Sodium Carbonate:
Add a small spatula of sodium carbonate to a test tube.
Carefully add 2 cm³ of dilute ethanoic acid using a pipette.
Collect the gas produced and bubble through limewater.
If limewater turns cloudy, a carboxylic acid is confirmed (due to CO2 production).
Test for Halogenoalkanes
Nucleophilic Substitution:
Add 5 drops of 1-bromobutane to 1 cm³ ofNaOH in a test tube.
Warm in a water bath at approximately 60°C.
Acidify with 2 cm³ of dilute nitric acid and add 1 cm³ ofAgNO3.
Observe the precipitate:
White precipitate for chloride ions.
Cream precipitate for bromide ions.
Yellow precipitate for iodide ions.
Results
Test
Reagent Used
Observation
Conclusion
Alcohol (Sodium Test)
Metallic sodium
Bubbles of hydrogen gas; "squeaky pop" with a lit splint
Presence of an alcohol confirmed
Alcohol (Dichromate)
Acidified potassium dichromate
Orange to green for primary/secondary alcohol; remains orange for tertiary
Identifies primary/secondary or tertiary alcohol
Aldehyde
Fehling's solution
Formation of a brick-red precipitate
Presence of an aldehyde confirmed
Alkene
Bromine water
Decolourises from orange to colourless
Presence of an alkene confirmed
Carboxylic Acid
Sodium carbonate
Effervescence, limewater turns cloudy
Presence of a carboxylic acid confirmed
Halogenoalkane
NaOH, dilute nitric acid, silver nitrate
White, cream, or yellow precipitate
Identifies Cl−,Br−,orI− ions based on precipitate colour
infoNote
Summary
Alcohols are tested by reaction with sodium and colour change with potassium dichromate.
Aldehydes are detected using Fehling's solution, producing a red precipitate.
Alkenes cause bromine water to lose its orange colour, confirming unsaturation.
Carboxylic acids release CO₂ when reacting with sodium carbonate, turning limewater cloudy.
Halogenoalkanes react with NaOH and AgNO₃ to form characteristic coloured precipitates based on the halogen.
Errors and Improvements
Errors:
Misinterpreting subtle colour changes.
Cross-contamination between test tubes affecting results.
Improvements:
Use new test tubes for each test to avoid contamination.
Perform colour tests in well-lit conditions to improve observation accuracy.
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