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Notes

Organic chemistry — section overview

Organic chemistry is the study of carbon-containing compounds. Section C7 covers hydrocarbons (alkanes and alkenes), alcohols, carboxylic acids, esters, and polymer chemistry.

Hydrocarbons

Alkanes: CₙH₂ₙ₊₂ (saturated — all single bonds)

  • Methane CH₄, Ethane C₂H₆, Propane C₃H₈, Butane C₄H₁₀

Alkenes: CₙH₂ₙ (unsaturated — at least one C=C double bond)

  • Ethene C₂H₄, Propene C₃H₆

Test for alkenes: add bromine water; decolourises (turns from orange-brown to colourless) as bromine adds across the C=C bond.

Combustion of hydrocarbons

  • Complete combustion (excess O₂): hydrocarbon + O₂ → CO₂ + H₂O
  • Incomplete combustion (limited O₂): produces CO (toxic) and carbon (soot)

Crude oil and fractional distillation

Crude oil is a mixture of hydrocarbons separated by fractional distillation. Smaller molecules (shorter chains): lower boiling point, more flammable, less viscous, more volatile.

Cracking: breaking down long-chain alkanes into shorter, more useful alkanes + alkenes (using high temperature and catalyst/steam).

Alcohols

General formula: CₙH₂ₙ₊₁OH. Example: ethanol (C₂H₅OH).

  • Combustion: C₂H₅OH + 3O₂ → 2CO₂ + 3H₂O
  • Fermentation: glucose + yeast → ethanol + CO₂ (at ~25–35°C, anaerobic)
  • Reaction with carboxylic acids → ester + water (condensation/esterification)

Carboxylic acids

General formula: CₙH₂ₙ₊₁COOH. Example: ethanoic acid (CH₃COOH — vinegar). Weak acids; react with metals, carbonates and alcohols.

Esters

Formed when alcohol + carboxylic acid react (with acid catalyst). Used as perfumes and food flavourings. Example: ethanol + ethanoic acid → ethyl ethanoate + water.

Addition and condensation polymerisation

Addition polymerisation: many alkene monomers join together — C=C bonds open up. n(CH₂=CH₂) → (−CH₂−CH₂−)ₙ (poly(ethene))

Condensation polymerisation (HT): monomers with two functional groups join, releasing small molecules (H₂O or HCl).

Common exam mistakes in C7

  1. Alkanes are saturated — all single bonds — alkenes are unsaturated (C=C)
  2. Bromine water test — colour lost with alkenes — alkanes do NOT decolourise bromine water
  3. Fermentation — anaerobic, ~25°C — too hot = enzyme denatured; too cold = slow

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Practice questions

Try each before peeking at the worked solution.

  1. Question 14 marks

    Alkanes vs alkenes

    Distinguish between alkanes and alkenes. Describe how you would distinguish between them in the lab.

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  2. Question 24 marks

    Fermentation

    Describe the conditions required for fermentation of glucose to produce ethanol.

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  3. Question 34 marks

    Cracking

    Explain why cracking of hydrocarbons is economically important. Include the conditions needed.

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  4. Question 43 marks

    Addition polymerisation

    Draw the repeat unit of poly(propene) from the monomer propene (CH₂=CHCH₃).

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  5. Question 55 marks

    Esterification

    Ethanol reacts with ethanoic acid. Name the products and state the conditions for the reaction.

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Flashcards

C7 — Organic chemistry

Key terms for AQA GCSE Chemistry Section C7.

10 cards · spaced repetition (SM-2)