00:01
Let's complete the following reactions by drawing the products and indicating all stereo isomers that are formed.
00:10
For a, we have cyclo -hex 2 -n -oan.
00:28
This is going to react with ch3 -2 -c -u -l -i and h -3 -2 to produce two isomers here.
01:16
We would have s -3 -methyl cyclo -hexanone.
01:30
And we would have over here, r -3 -methyl, more space here, r -3 -methyl cyclo -hexanone.
02:02
And those would be our two products.
02:07
For b, again starting from cyclo -hex -2 -anone, react this with ch3 mgbr and h3o plus will produce two ismers here we would have r 1 methyl cyclo 2 and all and we would have s 1 methyl cyclo hex 2 two and all.
03:40
Those would be our two products for b.
03:48
For c, starting from propiofenone and pyrrolidine, reacting with a trace amount of acid.
04:38
We will produce two products...