IGCSE Chemistry 0620 · Common mistakes

Common mistakes in IGCSE organic chemistry

Updated · by the Fahmazing team

Organic chemistry is full of names that look alike and reactions that sound alike. These are the slips that most often cost marks, each shown next to the answer that earns them.

Saying bromine water turns "clear"

Clear means see-through, and orange bromine water is already clear. The mark scheme wants colourless.

What is seen when ethene is bubbled through bromine water?

✗ Wrong: It turns from orange to clear.

✓ Right: It turns from orange to colourless.

Free lesson: Alkenes

Giving alkanes the reactions of alkenes

Only alkenes (with a C=C bond) decolourise bromine water or undergo addition. Alkanes are saturated. With chlorine in UV light they undergo substitution: one H swaps for one Cl.

Methane reacts with chlorine in UV light.

✗ Wrong: CH₄ + Cl₂ → CH₄Cl₂ (addition)

✓ Right: CH₄ + Cl₂ → CH₃Cl + HCl (substitution)

Free lesson: Alkanes

Writing carbon monoxide for complete combustion

With plenty of oxygen, an alkane burns to carbon dioxide and water. Carbon monoxide and soot come from incomplete combustion.

Complete combustion of methane

✗ Wrong: CH₄ + O₂ → CO + 2H₂O

✓ Right: CH₄ + 2O₂ → CO₂ + 2H₂O

Free lesson: Alkanes

Balancing only the carbon in cracking

Both sides must have the same number of carbon and hydrogen atoms. Subtract both.

C₁₀H₂₂ → C₈H₁₈ + ?

✗ Wrong: C₂H₂

✓ Right: C₂H₄ (ethene): 10 − 8 = 2 carbons and 22 − 18 = 4 hydrogens

Tip: Cracking needs both a high temperature and a catalyst. Giving only one loses the mark.

Free lesson: Alkenes

Mixing up the two ways to make ethanol

Fermentation uses yeast at 25–35 °C with no oxygen: slow but renewable. Hydration of ethene uses steam at about 300 °C and 6000 kPa with an acid catalyst: fast and continuous, but uses ethene from petroleum.

State the conditions for fermentation.

✗ Wrong: 300 °C with an acid catalyst

✓ Right: Yeast, 25–35 °C, in the absence of oxygen

Free lesson: Alcohols

Confusing ethanol, ethanoic acid and ethanoate

Look at the ending: -ol is an alcohol, -oic acid is a carboxylic acid, and salts of ethanoic acid are ethanoates.

Name the salt formed from ethanoic acid and sodium hydroxide.

✗ Wrong: Sodium ethanol

✓ Right: Sodium ethanoate

Free lessons: Carboxylic acids · Naming organic compounds

Naming an ester the wrong way round

The alcohol gives the first word (ending -yl); the acid gives the second (ending -oate).

Ester from ethanol and propanoic acid

✗ Wrong: Propyl ethanoate

✓ Right: Ethyl propanoate

Free lesson: Naming organic compounds

Leaving the C=C in a polymer

In addition polymerisation each C=C opens and links to the next monomer. The repeat unit has only single C–C bonds in the chain, and no other product forms.

Repeat unit of poly(ethene)

✗ Wrong: –CH₂=CH₂–

✓ Right: –CH₂–CH₂–

Free lesson: Polymers

Questions students ask

How do you test for an alkene?

Add bromine water. An alkene turns it from orange to colourless. An alkane leaves it orange.

What is the difference between addition and substitution?

In addition, atoms join across a C=C double bond and one product forms. In substitution, one atom swaps for another, so there are two products, such as CH₃Cl and HCl.

Why is fermentation done without oxygen?

With oxygen, yeast respires aerobically and ethanol can be oxidised to ethanoic acid, so little ethanol is made.

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