Structure, Bonding & Reactivity (AQA AS Chemistry): Revision Note

Exam code: 7404

Stewart Hird

Written by: Stewart Hird

Reviewed by: Philippa Platt

Updated on

Shapes & Bond Angles in Organic Molecules

  • Carbon has four electrons in its outer shell (electronic configuration: 1s² 2s² 2p²)

  • To achieve a full outer shell, carbon forms four covalent bonds by sharing its four outer electrons with other atoms

  • Covalent bonds are formed by the overlap of atomic orbitals

    • There are two types of covalent bonds: sigma (σ) bonds and pi (π) bonds

  • A sigma bond is formed by the direct overlap of orbitals along the line between two nuclei

  • In a carbon–carbon double bond, each carbon forms three sigma bonds using three of its outer electrons

    • The remaining electron occupies a p orbital

  • When the unhybridised p orbitals on two carbon atoms overlap sideways, a pi bond is formed

    • The π bond contains two electrons and lies above and below the plane of the atoms

  • The three regions of electron density around each carbon repel equally, resulting in a trigonal planar shape with bond angles of approximately 120°

The bonding in ethene

  • In ethene (C2H4), each carbon atom uses three of its four outer electrons to form sigma (σ) bonds

  • Two σ bonds are formed between each carbon atom and two hydrogen atoms

  • One σ bond is formed between the two carbon atoms

  • The remaining electron on each carbon atom occupies an unhybridised p orbital

    • These p orbitals overlap sideways to form a pi (π) bond

  • As a result, the carbon–carbon bond in ethene is a double bond, consisting of one σ bond and one π bond

Diagram of ethene showing p orbitals forming pi bonds and s orbitals forming sigma bonds, with bond angles of 120 degrees and planar structure.
Sigma and pi bonds in ethene
Diagram of a chemical structure showing sigma and pi bonds, hydrogen nuclei marked as "X" in red lobes, carbon nuclei as black dots.
The shape of the molecular orbitals in an ethene molecule

Examiner Tips and Tricks

A double bond consists of one sigma (σ) bond and one pi (π) bond. A triple bond consists of one sigma bond and two pi bonds.

Bond strength increases in the order: single < double < triple.

This is because multiple bonds have greater electron density between the nuclei and additional orbital overlap, resulting in stronger electrostatic attraction and a shorter, stronger bond.

You should be able to draw and explain sigma and pi bonding diagrams clearly in the exam.

Molecular Orbitals

Orbital overlap in covalent bonds

  • A single covalent bond is formed when two atoms, usually non-metals, share a pair of electrons

  • Each atom contributes one unpaired electron from an atomic orbital

    • When the bond forms, these atomic orbitals overlap to produce a shared region of electron density containing two electrons

    • This region of electron density can be described as a bonding molecular orbital

  • The greater the overlap between the atomic orbitals, the stronger the bond formed

  • Sigma (σ) bonds are formed by end-to-end (axial) overlap of orbitals along the line between the two nuclei

  • Pi (π) bonds are formed by the sideways overlap of parallel p orbitals, creating regions of electron density above and below the sigma bond

σ bonds

  • Sigma (σ) bonds are formed from the end-to-end overlap of atomic orbitals

  • s orbitals overlap this way, as well as p orbitals

Diagram showing two s atomic orbitals combining to form a molecular sigma orbital in a hydrogen molecule, with labels and a right-pointing arrow.
Sigma orbitals can be formed from the end to end overlap of s orbitals 
  • In a sigma (σ) bond, the electron density is symmetrical about the line joining the nuclei of the two bonded atoms

  • The shared pair of electrons is located directly between the nuclei

  • The bond is formed due to the electrostatic attraction between the negatively charged shared electrons and the positively charged nuclei of both atoms

 Hydrogen

  • The hydrogen atom has only one s orbital

  • The s orbitals of the two hydrogen atoms will overlap to form a σ bond

Two hydrogen atoms with 1s orbitals form a covalent bond, producing a diatomic hydrogen molecule with a sigma bond indicated.
The formation of a molecular orbital in the hydrogen molecule

π bonds

  • Pi (π) bonds are formed by the sideways overlap of parallel p orbitals on adjacent atoms

  • The overlapping p orbitals create regions of electron density above and below the plane of the sigma (σ) bond.

  • This sideways overlap allows effective orbital interaction and forms a single π bond

  • A π bond is often represented as two electron clouds, one above and one below the plane of the nuclei.

    • Together, these two regions of electron density contain one shared pair of electrons, forming one π bond 

Diagram showing p atomic orbitals combining to form a molecular orbital, which forms a JT bond, explained with labelled boxes and arrows.
π orbitals can be formed from the sideways overlap of p orbitals

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Stewart Hird

Author: Stewart Hird

Expertise: Chemistry Content Creator

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Topic Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.

Philippa Platt

Reviewer: Philippa Platt

Expertise: Chemistry Content Creator

Philippa has worked as a GCSE and A level chemistry teacher and tutor for over thirteen years. She studied chemistry and sport science at Loughborough University graduating in 2007 having also completed her PGCE in science. Throughout her time as a teacher she was incharge of a boarding house for five years and coached many teams in a variety of sports. When not producing resources with the chemistry team, Philippa enjoys being active outside with her young family and is a very keen gardener