 everyone let's try this one together and says give the major product of the following reaction. So what kind of reaction are we actually doing? What kind of mechanism is this going through? Radical reaction mechanism. So that means that we got to find where the most stable radical is going to be, right? So we have the option of a primary, a tertiary, a secondary, a primary, a primary, right? Where's it going to go? Tertiary. Tertiary, right? Because the tertiary is the most stable, okay? So that's where it's going to go. So when we write the product, where are we going to put the bromine? Tertiary. Tertiary. So on this carbon here, right? Okay, so what we're going to do is actually take that hydrogen away and substitute it for bromine, okay? That's what's going to happen. So it just wants the major organic products, so I don't have to put HBR or all that stuff, okay? So just the major organic product. Any questions on that one? Some people like to do it online, like I normally like to do it. If it's wedges and dashes, you're saying? Yeah. Yeah, in this case, right, there's no stereo center there because there's two methyl groups. So you don't have to do wedges and dashes in the case where there's no stereo center. Okay. Any other questions? Wonderful.