Great tutorial here, Sir! At 3:40, you discussed how -OH abstracts the H from the amide group and uses that to protonate the OH, leaving as H₂O. What about the possibility of proton transfer from the amide to the OH directly?
Thank you so much sir for this video. Can u please tell the mechanism for the reaction when thioacetal goes under reduction in the presence of raney nickel
There isn’t a clear mechanism because Zn has too much electrons and nowadays anyone discovered a mechanism; there aren’t publications in organic chemistry literature. Some chemists suggest that Zn make a complex and this is another chemistry field( coordination compounds).
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You are just great , one of the best organic chemistry teacher
One of the best teachers in general
Thank you, I have my 12th grade mid term exam today and I needed to clear my concepts on orgo.
Are you indian?
@@ankushshenoy4747 yeah ofc he is
How did your midterm go?
Sir you are veeeeeeeery greaaaaat your lectures solved me alot of problems which i faced from about 3 years
I highly recommend illustrating that the hydroxyl group is protonated and therefore good enough to act as a leaving group.
the solution is basic kid
In basic medium 🤨🤨
he said it's not a good leaving group, but hydroxyl can displace itself
Your video helps me a lot!!!!!!!!!!!
Great tutorial here, Sir! At 3:40, you discussed how -OH abstracts the H from the amide group and uses that to protonate the OH, leaving as H₂O. What about the possibility of proton transfer from the amide to the OH directly?
Thank you so much sir for this video. Can u please tell the mechanism for the reaction when thioacetal goes under reduction in the presence of raney nickel
It's in the aldehydes & ketones video in the organic chemistry playlist.
Please tell the mechanism for Clemensen reduction
There isn’t a clear mechanism because Zn has too much electrons and nowadays anyone discovered a mechanism; there aren’t publications in organic chemistry literature. Some chemists suggest that Zn make a complex and this is another chemistry field( coordination compounds).
@@antoniomultari881 oh okay..
great work sir
Wonderful..
So if one were to, and strictly in hypothetical, use Wolff-kishner on methylpropiophenone, would it yield the alkane?
yeah, why not
Hydroxyl is not a LG. You forgot to protonate it before removing it.
It's a alkaline solution mate
U can protonate it in acidic Sol.
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