Meet Carbon

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Model of a carbon atom

Why does carbon build countless compounds?

In the periodic table, carbon is in Group 14, Period 2.

With four valence electrons, it is tetravalent and forms four strong covalent bonds.

Strong C–C bonds allow extensive self-linking, called catenation, creating chains, rings and networks.

Quick check: How many covalent bonds can a single carbon atom form?

Key Points:

  • Position: Group 14, Period 2.
  • Tetravalency → 4 covalent bonds.
  • Catenation forms long chains and rings.
  • These traits explain carbon’s vast number of compounds.

Covalent Bonding

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Electron sharing in a hydrogen molecule (H₂)

H₂: A Model Covalent Bond

Atoms that cannot easily lose or gain electrons become stable by sharing them.

In H₂, each hydrogen shares one electron; the pair forms a covalent bond and completes the 2-electron duplet for both atoms.

Key Points:

  • Electron sharing binds the two atoms.
  • Each H achieves a stable duplet (2 electrons).
  • A covalent bond is a shared pair of electrons.

Single vs Double …and Triple Bonds

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Counting Bond Pairs

Atoms share electrons as discrete bond pairs.

The number of shared pairs decides the bond order.

More pairs make bonds shorter and stronger.

Key Points:

  • Single bond: 1 pair; longest, weakest. Example \( \text{H}_2 \).
  • Double bond: 2 pairs; shorter, stronger. Example \( \text{O}_2 \).
  • Triple bond: 3 pairs; shortest, strongest. Example \( \text{N}_2 \).

Example: Methane

Electron-dot diagram of methane (CH₄)

Electron-dot diagram of methane (CH₄)

How the dots add up

Carbon shares its four valence electrons with four hydrogens in a tetrahedral sharing pattern.

The molecule is a saturated hydrocarbon; each C–H bond is single and every atom reaches stability.

Key Points:

  • Place C in the centre; set 4 H at the corners of a tetrahedron.
  • Draw one shared electron pair between C and each H.
  • Check: C now has 8 electrons, every H has 2.

Carbon Allotropes

Diamond

Each carbon makes 4 covalent bonds in a 3-D tetrahedral lattice.
Hardest natural material; very high melting point; does not conduct electricity.
Used in cutting, drilling and sparkling jewellery.

Graphite

Each carbon bonds to 3 others forming flat hexagonal layers.
Layers held by weak forces, so they slide; soft and slippery.
Delocalised electrons make graphite a good electrical conductor.
Used in pencils, dry lubricants and electrodes.

Key Similarities

Pure carbon allotropes—no other elements present.
Strong C–C bonds give high melting points and chemical stability.
Fullerene (C60) forms closed cages; used in nano-electronics and drug delivery.

Saturated vs Unsaturated

Unsaturated ethene molecule with double bond highlighted

Ethene (C₂H₄) shows a carbon–carbon double bond.

How to spot saturation

Alkanes are saturated: each carbon forms four single bonds.

Alkenes contain at least one C=C double bond, making them unsaturated and more reactive.

Key Points:

  • Single bonds only → saturated alkane.
  • A C=C or C≡C means the molecule is unsaturated.
  • Spot the double bond in ethene to classify it as an alkene.

Isomer Magic

Structural isomers of butane

Straight-chain (n-butane) vs branched (iso-butane)

Structural Isomers of Butane

Butane \( \mathrm{C_4H_{10}} \) exists as two structural isomers.

n-butane forms a straight carbon chain, while iso-butane branches at the central carbon.

Same formula, new layout—this change alters boiling point and other properties.

Key Points:

  • Same molecular formula: \( \mathrm{C_4H_{10}} \)
  • Different layout: chain vs branched
  • Leads to different physical properties

Multiple Choice Question

Question

Applied recall: Identify the unsaturated hydrocarbon.

1
C₂H₆
2
C₂H₄
3
CH₄
4
C₃H₈

Hint:

Unsaturated molecules show at least one C=C or C≡C bond.

Key Takeaways

Summary & Next Steps

Tetravalency

Carbon forms four covalent bonds, creating countless stable molecules.

Catenation

Carbon chains, rings and networks multiply structural variety.

Saturation & Isomerism

Single or multiple bonds and varied atom order create saturated, unsaturated and isomeric compounds.

Allotropes

Diamond, graphite and others show carbon’s wide property range.

Next Steps

Practise IUPAC naming and draw structural formulas to reinforce these key ideas.