I was toiling over a problem where there were secondary and primary amines and kept "attacking" the secondary amines until I watched this video. Thanks for helping me realize the stability of imines over enamines.
If i understand the Ozasone formation mechanism in a couple of hours (7:30 am class) i'll have extra points on my test (april 16) this step is the problem, thanks a lot! :)
Hi, why can't the amine act directly as a nucleophile, attacking the partial positively charged carbon of the carbonyl group? and follows the mechanism of nucleophilic addition?
I was toiling over a problem where there were secondary and primary amines and kept "attacking" the secondary amines until I watched this video. Thanks for helping me realize the stability of imines over enamines.
Kyle Judd lol glad to see you're strengthening your physical science! :)
I swear,it can't be better than this...superbly explained
If i understand the Ozasone formation mechanism in a couple of hours (7:30 am class) i'll have extra points on my test (april 16) this step is the problem, thanks a lot! :)
It's very helpful to me Mr. But it's not clear for me to take notes 😢
Hi, why can't the amine act directly as a nucleophile, attacking the partial positively charged carbon of the carbonyl group? and follows the mechanism of nucleophilic addition?
It's very helpful to me Mr. But it's not clear for me to take notes 😢
It's very helpful to me Mr. But it's not clear for me to take notes 😢