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  • - [Instructor] What we're going to do in this video

  • is start talking about forces that exist between

  • even neutral atoms, or neutral molecules.

  • 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 proton and electrons.

  • And so 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

  • kinda 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's 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 an 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 moment,

  • where 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, lowercase 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 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 and 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 have

  • induce a dipole on the right hand side.

  • A dipole is just when you have

  • the separation of charge, where you have your

  • positive and 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

  • as 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,

  • which is usually associated with molar mass.

  • So usually molar mass,

  • then the higher polarizability you're gonna have.

  • 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, five, fifty electrons.

  • And that would create a stronger temporary dipole,

  • which would then induce a stronger dipole in the neighbor.

  • That could domino through

  • the entire sample of that molecule.

  • So for example, if you were to compare

  • some noble gases to each other.

  • 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 do 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 for 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 will have higher polarizability,

  • and higher London dispersion forces.

  • But also, the shape of the molecule matters.

  • The more that the molecules can come in contact

  • with each other, the more surface area

  • they have exposed to each other,

  • the more likely that they can induce

  • these dipoles in each other.

  • For example, butane can come in two different forms.

  • It can come in what's known as n-butane,

  • which looks like this.

  • So you have four Carbons and ten Hydrogens.

  • Two, three, four, five, six,

  • seven, eight, nine, ten.

  • This is known as n-butane.

  • But another form of butane known as iso-butane

  • would look like this.

  • Three Carbons in the main chain,

  • then you have one Carbon that breaks off of that

  • middle Carbon and then they all have four bonds.

  • And the left over bonds, you could say,

  • are with the Hydrogens.

  • So it would look like this.

  • This right over here is iso-butane.

  • Now if you had a sample of a bunch of n-butane,

  • versus a sample of a bunch of iso-butane,

  • which of these do you think will have

  • a higher boiling point?

  • Pause this video and think about that.

  • Well if you have a bunch of n-butanes next to each other,

  • imagine another n-butane right over here.

  • It's going to have more surface area

  • to its neighboring butanes because it is a long molecule

  • It can expose that surface area to its neighbors.

  • While the iso-butane in some ways

  • is a little bit more compact.

  • It has lower surface area.

  • It doesn't have these big long chains.

  • And so because you have these longer

  • n-butane molecules you're going to have

  • higher London dispersion forces.

  • They obviously have the same number of atoms in them.

  • They have the same number of electrons in them.

  • So they have similar sized electron clouds.

  • The have the same molar mass.

  • But because of n-butane's elongated shape,

  • they're able to get closer to each other

  • and induce more of these dipoles.

  • So just by looking at the shape of n-butane

  • versus iso-butane, you'd see higher

  • London dispersion forces in n-butane,

  • so its going to have a higher boiling point.

  • It's going to require more energy

  • to overcome the London dispersion forces

  • and get into a gaseous state.

- [Instructor] What we're going to do in this video

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