00:01
Is asking us to determine a mechanism after our f -moc, which is a protecting group, and this is the full structure of the f -mocon.
00:09
It's nine -floromethoxy -carboneal group.
00:13
So it's saying once this is treated with piperdine, what is our, what type of mechanism occurred? so we can look at our products and see that we formed there was a formation of an unprotected amino acid.
00:33
So our once protected amino acid bound with our fmoc, which is a protective group, as you can see how bulky the structure of it is.
00:44
Now we have an unprotected amino acid.
00:48
We also have co2.
00:50
So we know somewhere in there we lost a co2.
00:54
Or it was removed from a structure, and we can see that this fmac group has a c double bond o to two oxygens.
01:08
And then our byproduct, and we can see that this structure that's attached to what appears to be part of our fmac group, this structure is very similar to the formula for piperdine.
01:26
So a proposed mechanism, so from what we can kind of conclude is that there was probably a nucleophilic attack where the lone pair off of the nitrogen from the protected amino acid attacks the hydrogen group from the amine of piperdine.
01:55
So it attacks this hydrogen and this hydrogen will then leave and or the electrons will go back to this nitrogen...
