+Parakh Mody Anhydride hydrolysis doesn't generally need acid catalysis. It goes, A D E . Amide formation doesn't require acid catalysis either. For example from acid chloride, it would go, A D E as well.
That would be the reverse of step 2, which would get you back to the ester and water. It does happen, since the reaction is in equilibrium, but the reaction is driven to the right by choosing water as solvent.
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Ridiculous. This honorable man takes out from his valuable time to teach us something and you bitch about it! FYI in the settings you can decrease the speed ...
i love this video. thank you so much. i didn't know an auditory connection would help so much but it does!!!!
Thnank you...It helped me a lot remembering the 8 mechanism together..Easy way to remember...Liked it...Keep it up...
Thanks!
Thank you, Keep these videos up !
can you please tell me as to how the music can help me? cant find any relation between the music and the words
Ok it went above my head. Regular method suits me best. Thumbs of for trying.
YOU ARE AN AMAZING PERSON. THANK YOU!!!
Thanks, very good video, helpful for my final exam ~
Thanks ,its really fruitful for me.
Thanks! Keep up the good work!
Great video, James.
Was just curious, why not add in anhydride hydrolysis and amide formation to the list as well? 🤔
+Parakh Mody The video took 8+ hours to make and I thought it was long enough.
Okay, I was just wondering though, they would also follow the same mechanism (PADPED), right?
+Parakh Mody Anhydride hydrolysis doesn't generally need acid catalysis. It goes, A D E . Amide formation doesn't require acid catalysis either. For example from acid chloride, it would go, A D E as well.
thank you so much! I now understand it.
Good to hear from you Hannah Willis are you doing DAT prep?
The music lowkey calming my orgo stress
Please make a video on all types of substitution reaction i really need
Please explain why on the third step of the acid hydrolysis doesn't occur elimination insted of deprotonation
That would be the reverse of step 2, which would get you back to the ester and water. It does happen, since the reaction is in equilibrium, but the reaction is driven to the right by choosing water as solvent.
Do this for alkenes and alkynes!
Andres Vanegas hoping to get around to that! Have you seen my crash course on alkenes?
THANK YOU SO MUCH!!!
My perfect pitch was like “C D E C F E”???? 🤔😅😅
I love your videos can you please make some more
thank u ...it helps a lot....
I love this?
Thank you! If this video was helpful, you may want to check out our month-to-month MOC membership for access to over 1500 quizzes, Flashcards, the Reaction Guide, and more. Check it out here: bit.ly/2YctxPb
Does anyone hear the start of that one miley sirus song with that music haha
Like the woaoaaaoaoaooo caught in a bad romance bit
aaaaaaaaaaaay you talk too fast!!!
Ridiculous. This honorable man takes out from his valuable time to teach us something and you bitch about it! FYI in the settings you can decrease the speed ...