00:03
Okay, so here in the kup elimination, we are looking at nitro oxides.
00:09
Okay, so in these oxides, first i get the elimination, we basically get this an intra -molycular reaction where this oxide will attack the hydrogen here, and then same thing goes on.
00:32
The molecule.
00:35
Okay, and here we see the stem intermolecular elimination, creating a double bond between the alpha and the beta carbon, and then we leave off with a mean or hydroxamine.
00:51
Okay.
00:53
So then if i redraw this compound, basically, there's the overall mechanism.
01:00
Okay, so we have basically a quaternary amine as well, except this time it's been oxidized further.
01:20
Okay, so what will happen here is we need to look at the transition state of it.
01:28
Okay, so the transition state, there's a bond forming between the o and the h and a bond cleaving between this c and this h, the beta c, veta h okay so we'll just draw that dotted lines indicate line that's a partial bond okay and we know there is a delta minus here and as this one is getting taken away we are forming a delta minus while this one has a flow on positive charge remaining okay and yes since um the hydroxylamine is not a very good leaving group...