00:01
Okay, so here we're going to be comparing some hexene concepts.
00:05
So if we start off with one xe and we compare it to three hexene trans and three hexene cis, and then also look at a two two, a two, a two, five, dimethyl, petromethyl, one, two, two, and it's this.
00:39
So i've drawn a similar confirmation here.
00:45
Just compare all four of these molecules together.
00:49
Look at their multiple it's always a trans that are more stable than this is.
01:01
And that's because here we have the, now the ethanol groups in close proximity to each other at a very close angle.
01:11
While in trans, there are a lot for the more spreadable.
01:17
So trans is better than cis.
01:20
Also, like a substitution on an al -chain system helps stabilize it a lot through also with a hyper conjugation effect of the metals, basically just allowing those sp2 electrons to delocalize more and just, have some inductive effects as well.
01:48
So with that said, we can tell that basically this one is two, like a die substituted alkene, these three, well, this one is a monosputed.
02:00
So yeah.
02:02
So okay, for this one we can see, this is most stable.
02:05
Then afterwards, we can actually put this cis win here because it has a good amount of substitution plus a lot of extra metals to in that...