Intermolecular forces
Intermolecular forces
Identifying all intermolecular forces
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Keep the location of an attraction clear. Covalent bonds hold atoms together within a molecule. Intermolecular forces attract one molecule to another.
Start with induced dipole-dipole attractions, which act between all atoms and molecules. Polar molecules also have permanent dipole-dipole attractions. Suitable molecules can form hydrogen bonds as well.
List all the forces present before comparing substances. Naming hydrogen bonding does not mean the other applicable forces disappear.
London dispersion is another name for induced dipole-dipole interactions. Use the specific force name when explaining an attraction.
| Force | When present | Attraction |
|---|---|---|
| Induced dipole–dipole (van der Waals) | Between all atoms and molecules | Opposite instantaneous and induced partial charges |
| Permanent dipole–dipole | Also between polar molecules | Opposite permanent partial charges |
| Hydrogen bonding | H bonded to N/O/F and a neighbouring N/O/F lone pair | δ+ H bonded to N/O/F and a lone pair on N/O/F |
🧪 TEST IT
Work on paper. Attempt each question before opening its answer. These are original CrackingChem questions, written in AQA style.
- State the strongest intermolecular force in HCl. [1]
- State the strongest intermolecular force in CH4. [1]
- State the strongest intermolecular force in NH3. [1]
- State the strongest intermolecular force in CH3OCH3. [1]
- Explain why all four have van der Waals forces. [2]
Total: 6 marks
Show answer & marking points
- Permanent dipole–dipole [1].
- Induced dipole–dipole (van der Waals) [1].
- Hydrogen bonding [1].
- Permanent dipole–dipole [1].
- Continuously moving electrons produce instantaneous dipoles [1], which induce dipoles in neighbouring molecules and cause attraction [1].
Induced dipole–dipole (van der Waals) forces
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Electrons are always moving. For an instant, they can be distributed unevenly, giving one side of a particle a small negative charge and the other a small positive charge.
- This instantaneous dipole distorts the electron cloud of a neighbouring particle.
- That distortion creates an induced dipole in the neighbour.
- Opposite partial charges attract. New dipoles continually form as the electrons move.
A larger electron cloud is usually more easily distorted, or more polarisable. This tends to give stronger van der Waals attractions and a higher boiling point.
For isomers with the same electron count, more branching usually reduces surface contact between molecules. The overall attractions are then weaker, so less energy is needed to separate them.
| Factor | Consequence |
|---|---|
| More electrons / larger electron cloud | Greater polarisability, stronger temporary dipoles |
| Greater molecular surface contact | More neighbouring electron clouds can interact |
Halogen boiling-point trend
Explain Cl2 < Br2 < I2 in boiling point.
Worked answer
Electron number and polarisability increase down the group. van der Waals forces strengthen, requiring more energy to separate molecules.
🧪 TEST IT
Work on paper. Attempt each question before opening its answer. These are original CrackingChem questions, written in AQA style.
The table gives Group 0 data.
| Element | Number of electrons | Boiling point / °C |
|---|---|---|
| Ne | 10 | −246 |
| Ar | 18 | −186 |
| Kr | 36 | −153 |
| Xe | 54 | −108 |
- Name the force between the atoms. [1]
- Explain the trend from Ne to Xe. [4]
- Predict how Rn’s boiling point compares with Xe’s and justify your answer. [3]
Total: 8 marks
Show answer & marking points
- Induced dipole–dipole (van der Waals) forces [1].
- More electrons [1] give a more polarisable cloud [1], stronger temporary dipoles and attractions [1], requiring more energy to separate atoms [1].
- Above −108 °C [1]; more electrons / greater polarisability [1] give stronger van der Waals forces [1].
The three C5H12 isomers have the same electron count but different shapes.
| Compound | Boiling point / °C |
|---|---|
| Pentane | 36.1 |
| 2-Methylbutane | 27.8 |
| 2,2-Dimethylpropane | 9.5 |
- Place them in increasing volatility. [1]
- Explain why boiling points differ despite identical molecular formulae. [4]
Total: 5 marks
Show answer & marking points
- Pentane < 2-methylbutane < 2,2-dimethylpropane [1].
- Same electron count / similar potential for van der Waals forces [1]. More branching makes molecules compact and reduces surface contact [1]; attractions become weaker [1], so less energy is needed and boiling point falls [1].
Permanent dipole–dipole attractions
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A polar molecule has a permanent uneven distribution of charge. The δ+ end of one molecule attracts the δ− end of a neighbouring molecule.
These permanent dipole-dipole attractions act as well as induced dipole-dipole attractions. For otherwise comparable molecules, the extra attractions can increase the energy needed to separate them.
HCl has an overall dipole because it has one polar bond. SO₂ is bent, so its bond dipoles do not cancel. Use the shape as well as bond polarity when deciding whether this force is present.
Do not rank boiling points from polarity alone. A large non-polar molecule can have stronger overall attractions than a small polar molecule.
- Permanent dipole–dipole force
- Electrostatic attraction between the δ+ end of one polar molecule and the δ− end of a neighbouring molecule.
HCl versus F2
HCl and F₂ have similar relative molecular masses. Explain why HCl has the higher boiling point.
Worked answer
Both have van der Waals forces. HCl is polar and has additional permanent dipole–dipole attractions, increasing the energy needed to separate molecules.
🧪 TEST IT
Work on paper. Attempt each question before opening its answer. These are original CrackingChem questions, written in AQA style.
A student claims that the molecule with the largest permanent dipole must have the highest boiling point.
| Molecule | Dipole moment / D | Boiling point / °C |
|---|---|---|
| CH3F | 1.85 | −78 |
| CH3Cl | 1.87 | −24 |
| CH3Br | 1.82 | 4 |
| CH3I | 1.62 | 42 |
- Explain why all four have permanent dipoles. [2]
- Explain the boiling-point trend from CH3F to CH3I. [4]
- Evaluate the claim using the data. [2]
Total: 8 marks
Show answer & marking points
- C–X is polar [1]; unlike outer atoms make the tetrahedral molecule asymmetric, so dipoles do not cancel [1].
- More electrons [1], greater polarisability [1], stronger van der Waals forces [1], greater energy needed to separate molecules [1].
- False: CH3Cl has the largest dipole but CH3I boils highest [1]. van der Waals forces can dominate the total attraction [1].
All C–Cl bonds are polar.
| Molecule | Permanent dipole / D | Boiling point / °C |
|---|---|---|
| CH4 | 0 | −162 |
| CH3Cl | 1.87 | −24 |
| CH2Cl2 | 1.60 | 40 |
| CHCl3 | 1.04 | 61 |
| CCl4 | 0 | 77 |
- Identify the two non-polar molecules. [2]
- Explain why CCl4 has no permanent dipole despite polar C–Cl bonds. [2]
- Explain why boiling point rises from CH3Cl to CCl4 as permanent dipole decreases. [4]
- Evaluate “CCl4 has weaker intermolecular forces than CH3Cl because CCl4 has no permanent dipole.” [2]
Total: 10 marks
Show answer & marking points
- CH4 [1] and CCl4 [1].
- Symmetrical tetrahedral arrangement [1] makes four equal C–Cl dipoles cancel [1].
- Replacing H by Cl increases electron number [1] and polarisability [1], strengthening van der Waals forces [1] and increasing the energy needed to boil [1].
- False: both have van der Waals forces [1]; CCl4’s more polarisable cloud gives stronger overall attractions and a higher boiling point [1].
