 Okay, so we built this structure as an afterthought here, right? And we wanted to show the more favorable conformation and the least less favorable chair conformation, okay, since there were questions about that. So if we look here, right, we've got this molecule, one, four, trans, right? The two methyl groups are on opposite sides of the ring. One, four, trans, dimethylcyclohexane, okay? So here we see when we have that one, four, trans set up, we can see that axial up and axial down there, okay? So let's do a ring flip now, okay? So remember that equatorial bonds go to axial bonds go to equatorial when we do that ring flip, okay? So that twist boat is kind of the middle of the ring flip, actually. Okay, so let's do that. So now we see when we do that, right? What's happened to the two methyl groups? Yeah, they're equatorial. Yeah, they're equatorial. Do you see that, okay? So remember when we have those equatorial substituents, they're less or more favorable, right? Because they have less energetically unfavorable interactions with the other substituents. Specifically, they don't have, let's get back to this. They don't have what you see, the one, three diaxyl interaction there. Okay, that steric interaction where there's two groups trying to occupy that same place. You've got one, two, one, three diaxyls on the top and one, two, one, three diaxyls on the bottom. So that's quite unfavored relative to the equatorial version of this, the ring flip. Okay, are there any questions on that? No questions.