00:01
Okay, so we want to determine which of the phog alcohols will undergo dehydration faster when you treat with strong acid and heat.
00:08
The first one, we have these two alcohols.
00:26
So if we reacted with sulfuric acid and heat or some other strong acid, we're going to get a primary carbokadine in both cases.
00:34
But in this one, we get an allyl carbonatine, and this is more stable than a regular primary carbocadine because it can undergo a resonance, and it automatically makes it more stable.
00:47
So the fact that we have an allelial carbicadion is going to make this structure undergo the reaction faster.
00:55
And for b, we're comparing these two phenols, i mean these two rings.
01:12
So it's going to be the same case here, too, because we'll get a carbicadine right here, and this will be an allelicabotion.
01:22
It's automatically going to be more stable than the one that forms right here, because this can undergear resonance.
01:29
So this is going to be more stable again for the same.
01:32
Same reason as a.
01:57
Okay, so this is going to undergo dehydration faster because we'll get the formation of a tertiary carbonatein as opposed to this one, which is only secondary...