If you're seeing this message, it means we're having trouble loading external resources on our website.

If you're behind a web filter, please make sure that the domains *.kastatic.org and *.kasandbox.org are unblocked.

Main content

London dispersion forces introduction

London dispersion forces result from the electrostatic attraction between temporary dipoles. Dispersion forces are present between all molecules (and atoms) and are typically greater for heavier, more polarizable molecules and molecules with larger surface areas. Created by Sal Khan.

Want to join the conversation?

No posts yet.

Video transcript

- [Instructor] What we're going to do in this video is start talking about forces that exist between even neutral atoms or neutral molecules. And the first of these intermolecular forces we will talk about are London dispersion forces. So it sounds very fancy, but it's actually a pretty interesting and almost intuitive phenomenon. So we are used to thinking about atoms and let's just say we have a neutral atom, so it has the same number of protons and electrons, and so that's all those are all the protons and the neutrons in the nucleus. And then it'll have a cloud of electrons. So I'm just imagining all these electrons kind of jumping around. That's how I'm going to represent it. And let's imagine, and this is definitely not drawn to scale, the nucleus would actually be much smaller if it was. But let's say that there is an adjacent atom right over here and it's also neutral. Maybe it's the same type of atom, it could be different, but we're gonna say it's neutral. And it also has an electron cloud. And so if these are both neutral in charge, how would they be attracted to each other? And that's what London dispersion forces actually explain. Because we have observed that even neutral atoms and neutral molecules can get attracted to each other. And the way to think about it is electrons are constantly jumping around probabilistically. They're in this probability density cloud where electron could be anywhere at any given moment, but they're not always going to be evenly distributed. You can imagine that there is a moment where that left atom might look like this, just for a moment where most of, or maybe slightly more of the electrons are spending time on the left side of the atom than on the right side. So maybe it looks something like that. And so for that brief moment, you have a partial negative charge. This is the Greek letter delta, lower case delta, which is used to denote partial charge. And on this side, you might have a partial positive charge. Because remember, when it was evenly distributed, the negative charge was offset by the positive charge of the nucleus. But here on the right side, because there's fewer electrons here, maybe you have a partial positive on the left side, you have where most of the electrons are in that moment, partial negative. Now what might this induce in the neighboring atom? Think about that. Pause the video. Think about what might happen in the neighboring atom then? Well, we know that like charges repel each other and opposite charges attract each other. So if we have a partial positive charge out here on the right side of this left atom, well then the negative electrons might be attracted to it in this right atom. So these electrons here might actually be pulled a little bit to the left. So they might be pulled a little bit to the left. And so that will induce what is called a dipole. So now you'll have a partial negative charge on the left side of this atom, and then a partial positive charge on the right side of it. And we already had a randomly occurring dipole on the left-hand side, but then that would've induced a dipole on the right-hand side. A dipole is just when you have the separation of charge where you have your positive negative charges at two different parts of a molecule or an atom or really, anything. But in this world, then all of a sudden, these two characters are going to be attracted to each other or the atoms are going to be attracted to each other. And this attraction that happens due to induced dipoles, that is exactly what London dispersion forces is all about. You can actually call London dispersion forces is induced dipole, induced dipole forces. They become attracted to each other because of what could start out as a temporary imbalance of electrons, but then it induces a dipole in the other atom or the other molecule, and then they get attracted. So the next question you might ask is, how strong can these forces get? And that's all about a notion of polarizability. How easy is it to polarize an atom or molecule? And generally speaking, the more electrons you have. So the larger the electron cloud, larger electron cloud, electron cloud, which is usually associated with molar mass, so usually, molar mass, then the higher polarizability you're gonna have, 'cause you're just gonna have more electrons to play around with. If this was a helium atom, which has a relatively small electron cloud, you couldn't have a significant imbalance. At most, you might have two electrons on one side, which would cause some imbalance. But on the other hand, imagine a much larger atom or a much larger molecule, you could have much more significant imbalances. Three, four or five, 50 electrons. And that would create a stronger temporary dipole, which would then induce a stronger dipole in the neighbors. That could domino through the entire sample of that molecule. So for example, if you were to compare some noble gases to each other, and so we can look at the noble gases here on the right-hand side. If you were to compare the London dispersion forces between say, helium and argon, which one would you think would have higher London dispersion forces? A bunch of helium atoms next to each other, or a bunch of argon atoms next to each other? Well, the argon atoms have a larger electron cloud, so they have higher polarizability. And so you're going to have higher London dispersion forces. And you can actually see that in their boiling points. For example, the boiling point of helium is quite low. It is negative 268.9 degrees Celsius while the boiling point of argon, it's still at a low temperature by our standards, but it's a much higher temperature than the boiling point for helium. It's at negative 185.8 degrees Celsius. So one way to think about this, if you were at say, negative 270 degrees Celsius, you would find a sample of helium in a liquid state. But as you warm things up, as you get beyond negative 268.9 degrees Celsius, you're going to see that those London dispersion forces that are keeping those helium atoms together sliding past each other in a liquid state, they're going to be overcome by the energy due to the temperature. And so they're going to be able to break free of each other. And essentially, the helium is going to boil and you're going to enter into a gaseous state, the state that most of us are used to seeing helium in. But that doesn't happen for argon until a good bit warmer. Still cold by our standards. And that's because it takes more energy to overcome the London dispersion forces of argon because the argon atoms have larger electron clouds. So generally speaking, the larger the molecule, because it has a larger electron cloud, it'll have higher polarizability and higher London dispersion forces.