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London dispersion force

London dispersion force is a physics topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand London dispersion force rather than just read about it. In short: London dispersion forces (LDF, also known as dispersion forces, London forces, instantaneous dipole–induced dipole forces, fluctuating induced dipole bonds or loosely as van der Waals forces) are a type of intermolecular force acting between atoms and molecules that are normally electrically symmetric; that is, the electrons are symmetrically distributed with respect to the nucleus. They are part of the van der Waal…

London dispersion force — main illustration
London dispersion force — illustration

Key takeaways

  • London dispersion force belongs to physics; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect London dispersion force to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of London dispersion force from memory before moving on to harder problems.

Reference excerpt

London dispersion forces (LDF, also known as dispersion forces, London forces, instantaneous dipole–induced dipole forces, fluctuating induced dipole bonds or loosely as van der Waals forces) are a type of intermolecular force acting between atoms and molecules that are normally electrically symmetric; that is, the electrons are symmetrically distributed with respect to the nucleus. They are part of the van der Waals forces. The LDF is named after the German physicist Fritz London. They are the weakest of the intermolecular forces.

Introduction The electron distribution around an atom or molecule undergoes fluctuations in time. These fluctuations create instantaneous electric fields which are felt by other nearby atoms and molecules, which in turn adjust the spatial distribution of their own electrons. The net effect is that the fluctuations in electron positions in one atom induce a corresponding redistribution of electrons in other atoms, such that the electron motions become correlated. While the detailed theory requires a quantum-mechanical explanation (see quantum mechanical theory of dispersion forces), the effect is frequently described as the formation of instantaneous dipoles that (when separated by vacuum) attract each other. The magnitude of the London dispersion force is frequently described in terms of a single parameter called the Hamaker constant, typically symbolized A {\displaystyle A} . For atoms that are located closer together than the wavelength of light, the interaction is essentially instantaneous and is described in terms of a "non-retarded" Hamaker constant. For entities that are farther apart, the finite time required for the fluctuation at one atom to be felt at a second atom ("retardation") requires use of a "retarded" Hamaker constant. While the London dispersion force between individual atoms and molecules is quite weak and decreases quickly with separation R {\displaystyle R} like 1 / R 6 {\displaystyle 1/R^{6}} , in condensed matter (liquids and solids), the effect is cumulative over the volume of materials, or within and between organic molecules, such that London dispersion forces can be quite strong in bulk solid and liquids and decay much more slowly with distance. For example, the total force per unit area between two bulk solids decreases by 1 / R 3 {\displaystyle 1/R^{3}} where R {\displaystyle R} is the separation between them. The effects of London dispersion forces are most obvious in systems that are very non-polar (e.g., that lack ionic bonds), such as hydrocarbons and highly symmetric molecules like bromine (Br2, a liquid at room temperature) or iodine (I2, a solid at room temperature). In hydrocarbons and waxes, the dispersion forces are sufficient to cause condensation from the gas phase into the liquid or solid phase. Sublimation heats of e.g. hydrocarbon crystals reflect the dispersion interaction. Liquification of oxygen and nitrogen gases into liquid phases is also dominated by attractive London dispersion forces. When atoms/molecules are separated by a third medium (rather than vacuum), the situation becomes more complex. In aqueous solutions, the effects of dispersion forces between atoms or molecules are frequently less pronounced due to competition with polarizable solvent molecules. That is, the instantaneous fluctuations in one atom or molecule are felt both by the solvent (water) and by other molecules. Larger and heavier atoms and molecules exhibit stronger dispersion forces than smaller and lighter ones. This is due to the increased polarizability of molecules with larger, more dispersed electron clouds. The polarizability is a measure of how easily electrons can be redistributed; a large polarizability implies that the electrons are more easily redistributed. This trend is exemplified by the halogens (from smallest to largest: F2, Cl2, Br2, I2). The same increase of dispersive attraction occurs within and between organic molecules in the order RF, RCl, RBr, RI (from smallest to largest) or with other more polarizable heteroatoms. Fluorine and chlorine are gases at room temperature, bromine is a liquid, and iodine is a solid. The London forces are thought to arise from the motion of electrons.

… excerpt ends here. Continue reading the full article.

Illustrations

London dispersion force: Interaction energy of an argon dimer. The long-range section is due to London dispersion forces.
Interaction energy of an argon dimer. The long-range section is due to London dispersion forces.

Worked examples

Example 1 — a first encounter with London dispersion force

Start with the simplest possible case. Write down what London dispersion force claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In physics, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to London dispersion force before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about London dispersion force ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of London dispersion force

In research
London dispersion force appears in physics research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses London dispersion force in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
London dispersion force is common in secondary-school and first-year university syllabi. It links to neighbouring topics Chemical bonding, Intermolecular forces, so understanding it makes those chapters shorter.
In everyday life
Look for London dispersion force outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.

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How to study London dispersion force in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what London dispersion force means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain London dispersion force out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is London dispersion force in simple terms?

London dispersion forces (LDF, also known as dispersion forces, London forces, instantaneous dipole–induced dipole forces, fluctuating induced dipole bonds or loosely as van der Waals forces) are a type of intermolecular force acting between atoms and molecules that are normally electrically symmet…

Why does London dispersion force matter?

Because it connects several physics ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study London dispersion force?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on London dispersion force.

Tags

  • Chemical bonding
  • Intermolecular forces

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