Chemical bonding
Use H1 Chemistry bonding models to explain molecular shapes, polarity, intermolecular forces and the physical properties of solids.
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Before you begin
Every chemical bond is an electrostatic attraction, and the way electrons are shared or transferred decides how a substance behaves. This topic starts with ionic, covalent, dative and metallic bonds and the σ and π overlap behind covalent bonds. It then predicts molecular shapes, covers bond energy and polarity, explains intermolecular forces and the liquefaction of gases, and finishes by linking the structure of a solid to its physical properties.
Be comfortable with: O-Level bonding and structure, atomic orbitals and electron configuration.
Learning goals
- Describe the ionic bond as the electrostatic attraction between oppositely charged ions
- Describe the covalent bond as the electrostatic attraction between a shared pair of electrons and the positive nuclei
- Describe the metallic bond as the electrostatic attraction between a lattice of positive ions and delocalised electrons
- Describe ionic bonding in sodium chloride and magnesium oxide, using dot-and-cross diagrams
- Describe covalent bonding in H₂, O₂, N₂, Cl₂, HCl, CO₂, CH₄ and C₂H₄, using dot-and-cross diagrams
- Describe dative covalent bonding in the ammonium ion and Al₂Cl₆, using dot-and-cross diagrams
- Describe covalent bonding as overlap of s and p orbitals, forming σ and π bonds
- Use VSEPR theory to explain the shapes and bond angles of BF₃, CO₂, CH₄, NH₃, H₂O and SF₆
- Predict the shapes and bond angles of molecules similar to BF₃, CO₂, CH₄, NH₃, H₂O and SF₆
- Explain and deduce bond polarity from electronegativity
- Deduce whether a molecule is polar from its bond polarities and shape
- Describe intermolecular forces from permanent and induced dipoles, as in CHCl₃, Br₂ and the noble gases
- Describe hydrogen bonding, using ammonia and water as examples of molecules with –NH and –OH groups
- Outline how intermolecular forces allow gases to liquefy at high pressure or low temperature
- Outline how hydrogen bonding affects physical properties, including those of ice and water
- Explain bond energy and bond length for covalent bonds
- Compare how reactive covalent bonds are using bond energy, bond length and bond polarity
- Describe the ionic lattice of sodium chloride and magnesium oxide
- Describe the simple molecular lattice of iodine
- Describe the giant molecular lattices of graphite and diamond
- Describe the hydrogen-bonded lattice of ice
- Describe the metallic lattice of copper
- Describe, interpret and predict how structure and bonding affect a substance's physical properties
- Suggest the structure and bonding in a substance from given information
Syllabus statements covered
- show understanding that all chemical bonds are electrostatic in nature and describe: — ionic bond as the electrostatic attraction between oppositely charged ions
- show understanding that all chemical bonds are electrostatic in nature and describe: — covalent bond as the electrostatic attraction between a shared pair of electrons and positively charged nuclei
- show understanding that all chemical bonds are electrostatic in nature and describe: — metallic bond as the electrostatic attraction between a lattice of positive ions and delocalised electrons
- describe, including the use of ‘dot-and-cross’ diagrams, — ionic bonding as in sodium chloride and magnesium oxide
- describe, including the use of ‘dot-and-cross’ diagrams, — covalent bonding as in hydrogen; oxygen; nitrogen; chlorine; hydrogen chloride; carbon dioxide; methane; ethene
- describe, including the use of ‘dot-and-cross’ diagrams, — co-ordinate (dative covalent) bonding, as in formation of the ammonium ion and in the Al2Cl6 molecule
- describe covalent bonding in terms of orbital overlap (limited to s and p orbitals only), giving σ and π bonds (see also Section 9)
- explain the shapes of, and bond angles in, molecules such as BF3 (trigonal planar); CO2 (linear); CH4 (tetrahedral); NH3 (trigonal pyramidal); H2O (bent); SF6 (octahedral) by using the Valence Shell Electron Pair Repulsion theory
- predict the shapes of, and bond angles in, molecules analogous to those specified in (d)
- explain and deduce bond polarity using the concept of electronegativity [quantitative treatment of electronegativity is not required]
- deduce the polarity of a molecule using bond polarity and its molecular shape (analogous to those specified in (d))
- describe the following forces of attraction (electrostatic in nature): — intermolecular forces, based on permanent and induced dipoles, as in liquid and gaseous CHCl3, Br2 and the noble gases
- describe the following forces of attraction (electrostatic in nature): — hydrogen bonding, using ammonia and water as examples of molecules containing –NH and –OH groups
- outline the importance of intermolecular forces to the liquefaction of gases when subjected to high pressure and/or low temperature
- outline the importance of hydrogen bonding to the physical properties of substances, including ice and water
- explain the terms bond energy and bond length for covalent bonds
- compare the reactivities of covalent bonds in terms of bond energy, bond length and bond polarity
- describe, in simple terms, the lattice structure of a crystalline solid which is: — ionic, as in sodium chloride and magnesium oxide
- describe, in simple terms, the lattice structure of a crystalline solid which is: — simple molecular, as in iodine
- describe, in simple terms, the lattice structure of a crystalline solid which is: — giant molecular, as in graphite and diamond
- describe, in simple terms, the lattice structure of a crystalline solid which is: — hydrogen-bonded, as in ice
- describe, in simple terms, the lattice structure of a crystalline solid which is: — metallic, as in copper [the concept of the ‘unit cell’ is not required]
- describe, interpret and/or predict the effect of different types of structure and bonding on the physical properties of substances
- suggest the type of structure and bonding present in a substance from given information
Lessons
Work through them in order.
- Ionic and covalent bonding modelsDefine ionic, covalent and metallic attraction precisely and construct the required dot-and-cross representations.
- Dative bonding and common examplesExplain dative bonds in the ammonium ion and aluminium chloride as electron pairs donated by one atom.
- Sigma and pi bonds: orbital overlapRelate head-on and sideways orbital overlap to sigma and pi bonding.
- Molecular shapes and bond anglesPredict required shapes and angles using electron-region repulsion, including lone-pair effects.
- Bond energy, bond length and bond polarityConnect bond energy, length and electronegativity to bond and molecular polarity.
- Intermolecular forces and propertiesCompare intermolecular attractions and explain boiling points, miscibility and the properties of water and ice.
- Gas liquefactionExplain how cooling and compression allow intermolecular attractions to retain a liquid.
- Solids: structure and physical propertiesExplain lattice properties and deduce bonding and structure from combined physical evidence.
Practise and check
Or choose
Topic reference
Quick reference
| Question | First move | What to show |
|---|---|---|
| Define a bond | name the particles that attract | ionic: oppositely charged ions; covalent: a shared pair and both nuclei; metallic: positive ions and delocalised electrons |
| Dot-and-cross diagram | count the outer electrons | ions in brackets with charges; shared pairs and every lone pair |
| Dative bond | find a lone pair and an empty orbital | an arrow from the donor atom to the acceptor atom |
| σ and π bonds | count the bonded pairs of atoms | one σ per pair; one π per extra bond |
| Shape and bond angle | count the regions around the central atom | a multiple bond is one region; each lone pair closes the angle |
| Polar molecule? | bond polarity, then shape | whether the bond dipoles cancel |
| Boiling-point comparison | list the intermolecular forces in each | hydrogen bonding, electron-cloud size and molecular shape |
| Liquefaction | effect on kinetic energy and on separation | cooling slows molecules; compression brings them closer |
| Unknown solid | combine all the evidence | the structure, then each property from its particles and attractions |
Core knowledge to remember
- Ionic bond: the electrostatic attraction between oppositely charged ions.
- Covalent bond: the electrostatic attraction between a shared pair of electrons and the nuclei of the two bonded atoms.
- Metallic bond: the electrostatic attraction between a lattice of positive ions and delocalised electrons.
- In a dative bond, both electrons of the shared pair come from one atom. Once formed, it is an ordinary covalent bond.
- A single bond is 1σ; a double bond is 1σ + 1π; a triple bond is 1σ + 2π.
- Electron pairs repel: lone pair–lone pair > lone pair–bond pair > bond pair–bond pair. Shapes: linear 180°, trigonal planar 120°, tetrahedral 109.5°, trigonal pyramidal about 107°, bent about 104.5°, octahedral 90°.
- Bond energy is the energy needed to break one mole of a covalent bond in gaseous molecules. Shorter bonds are usually stronger.
- Electronegativity is the ability of an atom in a covalent bond to attract the shared pair.
- Hydrogen bonding needs an H bonded to N, O or F and a lone pair on N, O or F in another molecule.
- A substance conducts only if it has charged particles that can move: mobile ions or delocalised electrons.
Common mistakes
- Defining a bond by how it formed (“transfer”, “sharing”) instead of as an electrostatic attraction.
- Saying boiling or melting a simple molecular substance breaks covalent bonds.
- Counting a multiple bond as more than one region in VSEPR, or naming the electron-pair arrangement instead of the shape.
- Saying a molecule is polar because its bonds are polar, without checking whether the dipoles cancel.
- Naming hydrogen bonding whenever a molecule contains hydrogen.
- Saying pressure makes intermolecular forces stronger. It brings the molecules closer together.
- Explaining conductivity without naming the mobile charged particles in the stated physical state.