 Okay, so now we've got tert-butanol in here. Okay, remember the last time we did it we did ethanol Okay, so ethanol had a smaller alkyl group on there, right? Turt-butanol of course is going to have the bigger alkyl group on there So more alkyl group means what? Less acidic Less acidic, okay, so since it's less acidic would we expect this to react? Slower, right? So hopefully it does. Let's check it out Look how slow it's reacting, huh? Not doing really anything, huh? You can can we barely see any? See some hydrogen gas, right? Okay, let's put some phenol-thaline in there and see if we can see any Yeah, look how slow that's reacting. We'll get some agitation in here Yeah But still look how slow it is, right? Now let's head to the other ones So I don't know if we want to record this whole video of watching it Take its time in the tert-butanol or should we put some a little bit of water in there and see see it react really fast on this video Put a little bit of water And of course, you want to be careful when you're using sodium Very reactive and as Jim told us to remember it got really really hot So if we're gonna do this we're gonna turn this away from us Just put a little bit in there Yeah, you're reacting look how much faster it is. Any questions about what's going on with the I'm adding more and more alkyl groups. So let's try it one more time see if we can get it right for the video So when we add alkyl groups, what happens to the acidity? decreases very good, right? So Water then is more acidic than ethanol. Ethanol is more acidic than tert-butanol, right? Everybody okay with that? Okay, so I'm gonna kill it unless there are any more questions Okay, any more questions