Required Practical 5 • CH02 / CH05

RP5: Distillation of an Organic Product

Synthesize and isolate a volatile organic liquid via simple distillation, comparing partial oxidation of ethanol to ethanal versus complete oxidation under reflux to ethanoic acid.

1. Oxidation Reactions & Practical Aim

Required Practical 5 focuses on the preparation and separation of a volatile organic product. The classic reaction studied is the oxidation of primary alcohol ethanol (CH3CH2OH) using acidified potassium dichromate(VI) (K2Cr2O7 / H2SO4):

Partial Oxidation to Ethanal (Distillation Setup) CH3CH2OH + [O] → CH3CHO + H2O
- Reagents: Excess ethanol, limited acidified potassium dichromate(VI).
- Apparatus: Simple distillation (product is distilled off immediately to prevent further oxidation).
- Observation: Orange dichromate (Cr2O7^2-) is reduced to green chromium(III) (Cr3+).
Complete Oxidation to Ethanoic Acid (Reflux Setup) CH3CH2OH + 2[O] → CH3COOH + H2O
- Reagents: Excess acidified potassium dichromate(VI).
- Apparatus: Heating under reflux (condenser returned vertically to boiling flask to ensure complete oxidation before subsequent distillation).

2. Distillation vs Reflux Strategy: Boiling Point Hierarchy

The success of the synthesis depends on understanding the intermolecular forces and boiling points of the three compounds:

Compound Structure & Mr Predominant Intermolecular Forces Boiling Point Volatility
Ethanal CH3CHO (Mr = 44) Permanent dipole-dipole forces & London dispersion (no O-H hydrogen bonding) 21 deg C Very high (boils just below room temperature)
Ethanol CH3CH2OH (Mr = 46) Hydrogen bonding (due to polar O-H group) 78 deg C Moderate
Ethanoic Acid CH3COOH (Mr = 60) Extensive hydrogen bonding (forms stable cyclic dimers) 118 deg C Low
Why Distillation Isolates Ethanal Successfully

Because ethanal lacks an O-H bond, it cannot form intermolecular hydrogen bonds with itself. Its boiling point (21 deg C) is far lower than that of ethanol (78 deg C). In a simple distillation apparatus with gentle heating, ethanal vaporises the moment it forms, travels down the condenser, and is collected in an ice-cooled receiver before it can be further oxidised to ethanoic acid.

3. Quickfit Assembly Rules & Examiner Checklist

In Paper 5, candidates are regularly asked to identify errors in student sketches of distillation apparatus. The four critical assembly rules are:

1. Thermometer Bulb Alignment

The bulb of the thermometer must be placed level with the entrance to the side-arm of the still head. If placed too high, it reads low temperatures of stagnant air; if placed too deep in the flask, it measures superheated boiling liquid rather than the true boiling point of vapor entering the condenser.

2. Condenser Water Flow (In at Bottom, Out at Top)

Cold water must enter at the lowest nozzle (nearest the receiver) and exit at the highest nozzle (nearest the still head). This ensures the water jacket completely floods with no air pockets and provides maximum counter-current cooling efficiency.

3. Anti-Bumping Granules

Add 2 to 3 porcelain chips to the boiling flask before heating. They provide nucleation sites for smooth bubble formation, preventing explosive superheating (bumping) of liquid into the condenser.

4. Open Vent Safety (Never Seal the System)

The receiving adapter must have an open vent to the atmosphere. A completely sealed apparatus creates rapid pneumatic pressure buildup during heating, leading to violent glassware explosion.

Quickfit Simple Distillation Setup Quickfit Simple Distillation Apparatus Electric heating mantle (No naked flames) Thermometer bulb aligned with side-arm entrance Water OUT (top) Water IN (bottom) Ice-water bath Prevents ethanal (b.p. 21 deg C) from evaporating away

4. Step-by-Step Practical Protocol

  1. Carefully add 20 cm3 of acidified potassium dichromate(VI) solution into a 50 cm3 round-bottom flask.
  2. Cool the flask in an ice-water bath. Slowly add 5 cm3 of ethanol dropwise using a dropping pipette, swirling continuously to disperse heat (the reaction is highly exothermic).
  3. Add 2 to 3 anti-bumping granules to the flask.
  4. Clamp the flask securely and assemble the distillation apparatus: attach still head, thermometer, Liebig condenser, and receiving adapter.
  5. Connect the water hoses: cold tap water to bottom inlet, drain hose from top outlet to the sink. Turn tap on to achieve a steady, slow flow.
  6. Immerse the receiver flask into an ice-water bath. Ensure the system is open to the atmosphere via the adapter vent.
  7. Gently heat the boiling flask using an electric heating mantle or warm water bath.
  8. Collect the distillate boiling below 35 deg C (pure ethanal boils at 21 deg C).

5. Chemical Hazards & Laboratory Safety

Chemical Reagent Hazard Classification Precautionary Safety Control
Potassium dichromate(VI) (K2Cr2O7) Carcinogenic, mutagenic, toxic to reproduction, strong oxidiser. Wear nitrile gloves and safety goggles; avoid all skin contact; handle solid inside a fume cupboard.
Concentrated sulfuric acid (H2SO4) Severely corrosive; causes severe chemical burns. Add acid slowly to water/solution with cooling; never add water directly to concentrated acid.
Ethanol & Ethanal Highly flammable liquids and vapors. Eliminate all naked flames; use an electric heating mantle or hot water bath; keep ice bath cold.

6. Worked Yield Calculation Problem

Worked Example: Percentage Yield of Ethanal

Problem: A student oxidises 4.60 g of ethanol (Mr = 46.0 g mol^-1) to produce ethanal (Mr = 44.0 g mol^-1) via simple distillation. After purification, the mass of pure ethanal collected in the ice bath is 2.42 g.

Calculate the theoretical yield and the percentage yield of ethanal obtained in this preparation.

Step 1: Calculate moles of ethanol reactant

Moles of ethanol = mass / Mr = 4.60 / 46.0 = 0.100 mol

Step 2: Calculate theoretical yield of ethanal

Stoichiometry: 1 mol ethanol → 1 mol ethanal
Theoretical moles of ethanal = 0.100 mol
Theoretical mass = moles * Mr = 0.100 * 44.0 = 4.40 g

Step 3: Calculate percentage yield

Percentage Yield = (actual mass / theoretical mass) * 100
Percentage Yield = (2.42 / 4.40) * 100 = 55.0%

Final Answer: Percentage Yield = 55.0%

7. Practice Exam Questions

Question 1: In a simple distillation apparatus, why must water enter the condenser jacket at the bottom nozzle and leave from the top nozzle?

Show Answer & Explanation

Correct Answer: B

Introducing water at the bottom forces water to fill the entire cylindrical jacket before overflowing out the top, eliminating air bubbles that would leave sections of the condenser uncooled.

Question 2: Why is a Bunsen burner NEVER used to heat the reaction flask during the oxidation of ethanol to ethanal?

Show Answer & Explanation

Correct Answer: B

Ethanol and ethanal produce flammable vapors that can ignite upon exposure to open flames. An electric heating mantle or thermostated water bath must always be used.