how to do this mechanism if we're doing it in neutral condition. Amine directly attacks the aldehyde, but the double bond of the carbonyl wont shift right?
In theory, that would perform a reduction, but I have personally never seen something used in place of nabh3cn for this reaction. So I would say stick with nabh3cn unless your instructor uses something different.
thank you for showing the arrow pushing
Very helpful explanation, thank you so much!!
👍👍👍Next pls how to synthesis 1phenyl2propanone?? Thank you
Thank you for the video! Do you know what does the boron ends up turning into? some borate?
Thanks that was so much helpful!!!
You look too young for mr.Heisenberg... But anyway, here's your phenyl-propan-2-one.
So would this reaction work for reductive animation of n,n diethylamine to n,n Diethylmethylamine?
This is awesome bro thank you.
Can't you use LAH if you extract and purify the imine instead of doing a one pot reaction?
how to do this mechanism if we're doing it in neutral condition. Amine directly attacks the aldehyde, but the double bond of the carbonyl wont shift right?
When you add your NaCNBH3 do you still need to add acid to protonate the N or is there still H3O in your solution
Hii I have a question can we produce 1° aromatic amines from gabriel pthalimide synthesis???like aniline for example.
Can we use H2, raney Ni? Instead of nabh3cn?
In theory, that would perform a reduction, but I have personally never seen something used in place of nabh3cn for this reaction. So I would say stick with nabh3cn unless your instructor uses something different.
well done. subscribed
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yourrrrrrrrrrrrr welcomeeeee (thanks for watching!)