GCSE Chemistry • Topic 7

Organic Chemistry

Carbon-based compounds: from fuels to polymers.

📌 What You’ll Learn

  • Crude oil and fractional distillation
  • Alkanes: Properties and general formula
  • Alkenes and Cracking: Breaking long chains
  • Alcohols, Carboxylic Acids & Esters (Higher Tier)
  • Addition and Condensation Polymerisation

🧠 How to Study

  • Memorise the prefixes: Meth-, Eth-, Prop-, But-
  • Always count your Carbon bonds (must be 4!)
  • Link chain length to boiling point and viscosity
  • Practice drawing functional groups clearly
1. Crude Oil & Fractional Distillation (Separation)

What is Crude Oil?

A finite resource found in rocks. It is a mixture of many compounds, mostly hydrocarbons (compounds containing ONLY carbon and hydrogen).

How Fractional Distillation Works

Oil is heated until it evaporates. The column is hot at the bottom and cool at the top. Fractions condense at different levels based on their boiling points.

Chain Length Boiling Point Viscosity (Thickness) Flammability
Short (Top) Low Low (Runny) High
Long (Bottom) High High (Thick) Low
2. Alkanes (Saturated)

Structure and Formula

Alkanes are saturated hydrocarbons—they only have single C-C bonds. This means they contain as many Hydrogen atoms as possible.

General Formula: $$ C_nH_{2n+2} $$

Mnemonic: Mice Eat Paper Bags (Meth-, Eth-, Prop-, But-)

[Image showing the structural formulas of Methane, Ethane, Propane, and Butane]

Q1: What is the formula for an alkane with 5 Carbon atoms (Pentane)?

$$ C_5H_{(2 \times 5) + 2} = C_5H_{12} $$

3. Alkenes & Cracking (Unsaturated)

Alkenes

Alkenes are unsaturated because they contain at least one double C=C bond. They are much more reactive than alkanes.

General Formula: $$ C_nH_{2n} $$

Cracking

Breaking down long-chain hydrocarbons into smaller, more useful ones (short-chain alkane + alkene). This requires a catalyst and heat.

Q1: How do you test for an alkene?

Add Bromine Water. It will turn from orange/brown to colourless if an alkene is present.

4. Alcohols & Carboxylic Acids (Higher Tier)

Functional Groups

These are homologous series with specific groups of atoms that determine their reactions.

Series Functional Group Naming Suffix Example
Alcohols -OH -ol Ethanol ($CH_3CH_2OH$)
Carboxylic Acids -COOH -oic acid Ethanoic acid ($CH_3COOH$)
Esters -COO- -oate Ethyl ethanoate
[Image showing structures of Ethanol and Ethanoic acid]
⚠️ Exam Trap

In Ethanoic acid, the C=O and -OH are on the same carbon. Don't forget the double bond!

5. Polymers (Addition & Condensation)

Addition Polymerisation

Occurs when many small alkenes (monomers) join together. The double bond opens up to form a long chain.

Condensation Polymerisation (Higher Tier)

Involves monomers with two functional groups. When they react, they join together and lose a small molecule, usually water ($H_2O$).

Q1: What is the main difference between addition and condensation polymerisation?

Addition uses one monomer (alkene) and produces only the polymer. Condensation uses two different monomers and produces the polymer plus a small molecule like water.

⚡ Quick Revision Checklist

Key Formulas:
  • Alkanes: $C_nH_{2n+2}$
  • Alkenes: $C_nH_{2n}$
  • Alcohols: -OH group
  • Carboxylic Acids: -COOH group
Key Trends:
  • Longer chain = Higher boiling point
  • Longer chain = More viscous
  • Fractional distillation: Boiling point order
  • Saturated (single) vs Unsaturated (double)

🚫 Brutal Exam Trap Summary

1. Don't say hydrocarbons contain "carbon, hydrogen, and oxygen"; they ONLY contain C and H.
2. Don't forget that Alkenes turn bromine water colourless, not clear.
3. Don't confuse Alkane ($C_nH_{2n+2}$) and Alkene ($C_nH_{2n}$) formulas in calculations.
4. Don't forget that every Carbon atom must have exactly 4 bonds in your drawings.