Just stopping by to say you're awesome. Your mechanisms are always very complete and you explain why each step happens, its easy to follow and understand. You deserve more views!
Thank goodness for this video! My professor only showed us the reaction up to the imide and then told us we should be able to figure the rest out on our own 🤦♀
Omg I sincerely hope my professor doesn't want me to draw this monster. Both in class AND in my book, the whole mechanism was skipped over. they did the first few steps and then was just like "tadaah!" lol. So I came here to find the whole mechanism and now I see why they skipped so much of it....
I am still struggling with this synthesis and it is driving me nuts! Way too many arrows and steps! There must be a quick and dirty method! :-(. I don't want to memorize mechanisms... I want to actually know what it is I am doing.
before adding base, would the amine precipitate out of the reaction as a salt? That would make things a thousand times easier to handle in the subsequent reaction I'd like to perform.
I don't know if you already knew and edited in the recent video, but the movement of electrons of the intermediate where hydroxy group electrons collapse back is not correct. Not the double bond but the nitrogen should pick up the hydrogen so double bond's electron should be pushed to the nitrogen and that nitrogen should pick up the hydrogen. If a double bond directly pick up the electron, you won't have a neutral nitrogen with a new hydrogen added.
Just stopping by to say you're awesome. Your mechanisms are always very complete and you explain why each step happens, its easy to follow and understand. You deserve more views!
Justin Kwon I totally agree. He deserves more views and likes. I'm a subby!
love your videos! not to quick, and not too slow. Definitely a huge lifesaver in orgo 2. Thanks so much!
All I want is your name. I want to search you up😭😭😭. You've been my saviour ever since
julio gonzales
Thank goodness for this video! My professor only showed us the reaction up to the imide and then told us we should be able to figure the rest out on our own 🤦♀
you're the best tutor ever. thanks
Omg I sincerely hope my professor doesn't want me to draw this monster. Both in class AND in my book, the whole mechanism was skipped over. they did the first few steps and then was just like "tadaah!" lol. So I came here to find the whole mechanism and now I see why they skipped so much of it....
Yeah same
so true
Thank you so much 🙏🏻
I wanna die from this but i know i am gonna die so peacefully :) thx ya :D
Great explanations to each arrow of the mechanism - thanks!
Love you sir from India
10:15 I didn't understand from that part. There is only 4 carbon rings
Plz explain
I am still struggling with this synthesis and it is driving me nuts! Way too many arrows and steps! There must be a quick and dirty method! :-(. I don't want to memorize mechanisms... I want to actually know what it is I am doing.
Muchísimas gracias Bro! Saludos desde México.
Thank you so much!! Your videos are awesome and well explained, greetings from Mexico
before adding base, would the amine precipitate out of the reaction as a salt? That would make things a thousand times easier to handle in the subsequent reaction I'd like to perform.
Are you synthesizing drugs?
Superb bro
I don't know if you already knew and edited in the recent video, but the movement of electrons of the intermediate where hydroxy group electrons collapse back is not correct. Not the double bond but the nitrogen should pick up the hydrogen so double bond's electron should be pushed to the nitrogen and that nitrogen should pick up the hydrogen. If a double bond directly pick up the electron, you won't have a neutral nitrogen with a new hydrogen added.
KING
8:52
18:17
loved the video, hated the reaction 😢
yoooooooooooooooooooooo
too much stress