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- [Voiceover] Here we have one chair conformation of methylcyclohexane, and this is carbon one. You can see we have a methyl group that is axial up at carbon one. We also have a hydrogen, and I've made the hydrogen green so we can tell it apart from the other hydrogens. And this hydrogen is equatorial down at carbon one. Now, this chair conformation is in equilibrium with another chair conformation. And we can get to the other chair conformation by what we call a ring flip. So if I lift this carbon up, and I pull this other carbon down here, and then we rotate it a little bit, we can see the other chair conformation of methylcyclohexane, so here it is. Now, when we look at carbon one, we can see we have a difference now. At carbon one, the methyl group is now equatorial. Notice it's still up relative to the plane of the ring, but it's an equatorial methyl group. And the hydrogen is now axial, so it's still down, but it's an axial hydrogen. So that's what happens in a ring flip. We just saw the video of methylcyclohexane undergoing a ring flip, and now we have to draw our two chair conformation. So, we saw how to do this in an earlier video. If I'm trying to draw the chair conformation on the left, I start with two parallel lines that are offset from each other, so something like that. And then I draw a dotted line here, that intersects with the top point on the top line, and a dotted line that intersects with the bottom point on the bottom line. And next, we draw a line from the top dotted line down to the bottom, and then from the bottom up to the top, and those are parallel. And then finally, we have another set of parallel lines to give us a total of three sets of parallel lines. We start at carbon one, and we start axial up. So there's axial up, and then at carbon two would be axial down. Carbon three, axial up. Carbon four, axial down. Five is up, and six is down. Next we put in equitorial, so at carbon one we start equatorial down, so I draw that down. At two would be equatorial up. At three would be down. At four would be up. At five would be down, and six would be up. All right, this chair conformation is in equilibrium with another chair conformation. So let's go ahead and draw the other chair, and then I'll go back and put in the different groups. So for the other chair, we approach this the same way. We draw two parallel lines that are offset from each other, so those are my two parallel lines. And then we draw our dotted line that intersects pretty close to this top point here on the top line. And then we draw another dotted line, which is pretty close to this bottom point on the bottom line. Next, we put in another set of parallel bonds, so we put this one in, and then we draw-- Think about drawing a line parallel to that, so like that, and then finally we can go ahead and connect our dots. So we go like this, and these lines should be parallel too. Now, this is carbon one, and we do the opposite of what we did before. We start axial down. So, axial down at carbon one. This is carbon two, we go axial up. At carbon three is axial down. Carbon four, axial up. Carbon five, axial down. And finally, carbon six will be axial up. Go back to carbon one, and we're putting in the equatorial bonds now. Since we started axial down, then we would do equatorial up. So, this would be equatorial up, and then equatorial down at carbon two. At carbon three, would be equatorial up. At carbon four, equatorial down. At carbon five, equatorial up. And finally, at carbon six, equatorial down. Now, let's finally put in our groups. So, we go back up here to the diagram, and this was carbon one. We had a methyl group axial up. So, that methyl group is axial up, and go ahead and put in a C-H three, right here at carbon one. And then we have this green hydrogen here, which was equatorial down, if you look at how it's drawn. So, let me go ahead and put in that hydrogen. So, this is our green hydrogen. Let me go ahead and circle it and make it green so we can tell the difference here. And I could put in the other hydrogens, but I'm just not going to on our chair conformations. Okay, it's really good practice to draw all of these bonds, and you could put in the hydrogens, but I'm not worried about it. Our goal is to show the ring flip. So, at carbon one, let me go ahead and highlight it, this carbon one became this carbon, right here, when we did the ring flip. And notice what happened to our methyl group, just repeat what we saw in the video. We started axial up for our methyl group, and we still have this methyl group up, but notice it is now equatorial. So, we need to put in that methyl group equatorial at carbon one, so we go ahead and do that. Remember, this is carbon one. And then, our hydrogen, the green hydrogen, is still down relative to the plane of the ring, but is now axial. So this hydrogen right here is the green one. Let me go ahead and highlight it in green. It is now down, relative to our plane. So, the point of a ring flip is, any group that's axial becomes equatorial. Any group that's equatorial becomes axial. So that changes. But what doesn't change is, is it up or down relative to the plane of the rings? Let me go ahead and highlight this here. The methyl group stays up. So here, it's axial up, and over here, it's still up relative to the plane, but it turns equatorial. And what was down, which was our hydrogens-- Let me go ahead and highlight that here, this was equatorial down. The hydrogen stays down relative to the plane of the ring, but it turns axial. So you need to practice drawing all this stuff out. Now let's think about which conformation is more stable. So we have two chair conformations, and one is more stable than the other. And let's go back up to this picture here, and let's look at the interaction of this methyl group with these other axial hydrogens. So think about this hydrogen right here, and then this hydrogen right back here. This methyl group takes up a lot of space, and it's pretty close to these hydrogens in space. If you rotate this, there's some serious steric hindrance with putting the methyl group in the axial position. However, for this conformation on the right, with this methyl group out to the side in an equatorial position, now this methyl group doesn't really interfere with any of the axial hydrogens. So, down here, we have a hydrogen, right, which could interact a little bit with these other hydrogens but nowhere near as much as putting that methyl group in this position. So the goal with a relatively bulky substituent is to put it in the equatorial position, and that's going to be the most stable conformation. It turns out, at equilibrium, at room temperature, this conformation, this chair conformation on the right is about 95% of all the chair conformations of cyclohexane, and the one on the left is only about 5%. So, this is a substantial effect. The steric hindrance that destabilizes this conformation, you can call this a one, three diaxial interaction. So, if this is carbon one right here, so at carbon one we have something that's axial, and then this would be carbon two, and this would be carbon three. So, carbon three, we have something else that's axial. And these two can interfere with each other. So that's why we call this a one, three, diaxial-- So, two things that are axial, interaction. So, one, three diaxial interaction. It's the same idea for this hydrogen back here. And this steric hindrance destabilizes this conformation. The effect is even more pronounced when you have a larger group that's interfering with these axial hydrogens. For example, if we changed our group from a methyl group to a tert-butyl group, let me go down here so we can see a tert-butyl group. And I only drew part of the bonds here. Here you can see our tert-butyl group at carbon one, and if you think about one, three diaxial interactions, I could draw in some hydrogens here. Since you have all of these methyl groups here, this is going to be even more steric hindrance. And that's why at equilibrium, between these two conformations, 99.99% are going to be in this conformation, with your really bulky tert-butyl group equatorial and out to the side. That decreases the steric hindrance.