This was better than all the other videos I watched, my professor's lectures, and any website I read through. This is my first youtube comment ever because I was just so moved by this. Thank you, please keep up the amazing work :)
Bro your videos are just over the top 🔥, Chemistry isn't my strong zone ,but your videos clears any topic , it's really helpful brother. It pumps me up with enthusiasm to study it more. Thanks 😊❤️
Thx brother, love from india, i am a senior secondary school student, whe have more compounds in migratory aptitude, i was just having doubt on how these migratory aptitude series is made, and the way you thaught mechanism made it clear, more substituted alkene has more e* density and would want more to leave the - ve charged carbon and migrate, so thats how th decreasing series is made, thx bro again for solving my doubt, love from india❤😊
Hey awesome video, just a quick question: let's alpha to the C=O is a phenyl and a 2° carbon (technically 3°), from the migration priority list, these two are equal, would that reaction result in a mixture of both possible products?
Professor I have a few doubts kindly reply 🙇🏼♂️ 1. Can active methylene undergo this reaction? 2. Is there any effect if there are different functional groups are attached to the carbon attached to the primary carbon other than the ketone carbon?
@natsuuwu9290 check out ruclips.net/video/UE7X0pySAgE/видео.htmlsi=AYAdkEequ2xrai4-&t=1185 Here are the associated worksheet + written solutions: worksheets.joechem.io/worksheets/Predicting%20the%20Product%20of%20Reactions%20of%20Carbonyls.pdf worksheets.joechem.io/worksheets/Answer-%20Carbonyl%20Reaction%20Problems.pdf
Man ur tricks of adding oxygen between 2 carbon was easy but u r speaking really fast that's getting a bit towards a volatile memory be slow have some patience teacher
![I.N "HALLUCINATION" | [Stray Kids : SKZ-PLAYER]](http://i.ytimg.com/vi/n5B5q1Hwt_U/mqdefault.jpg)
![Seungmin "그렇게, 천천히, 우리(As we are)" | [Stray Kids : SKZ-PLAYER]](http://i.ytimg.com/vi/kAzmhLHePqU/mqdefault.jpg)
It seems you switched the stereochemistry of that top Bayer-Villiger Product at 10:15. The stereocenter was switched from S to R.
Ahhh you’re right, good catch
This was better than all the other videos I watched, my professor's lectures, and any website I read through. This is my first youtube comment ever because I was just so moved by this. Thank you, please keep up the amazing work :)
Rajika, thank you for watching and taking the time to leave such an incredibly nice comment :) I'm so pumped you found the video helpful!
I watched almost 10 videos for this topic , now I can say that I am satisfied ,than you so much sir 😊
Bro your videos are just over the top 🔥, Chemistry isn't my strong zone ,but your videos clears any topic , it's really helpful brother. It pumps me up with enthusiasm to study it more. Thanks 😊❤️
what a legend for posting this one
Most amazing Bayer villager video. I love it very much.
BEST EXPLANATION
Thx brother, love from india, i am a senior secondary school student, whe have more compounds in migratory aptitude, i was just having doubt on how these migratory aptitude series is made, and the way you thaught mechanism made it clear, more substituted alkene has more e* density and would want more to leave the - ve charged carbon and migrate, so thats how th decreasing series is made, thx bro again for solving my doubt, love from india❤😊
Best teacher
I hope to see you too
Best Ochem teacher ever ecisted
save me so much thnks bro
u the best
Thank you, I love your way of teaching.
THIS WAS SO AMAZING!! THANK YOU!!
This helped my understanding on my report. Thank you.
lovely man wth lovely lecture
You’re the best!
You are too good
thank you
Thanks man 👍👍👍 Keep it up 😃😃😃😃
Hey awesome video, just a quick question: let's alpha to the C=O is a phenyl and a 2° carbon (technically 3°), from the migration priority list, these two are equal, would that reaction result in a mixture of both possible products?
Thank you.
Professor I have a few doubts kindly reply 🙇🏼♂️
1. Can active methylene undergo this reaction?
2. Is there any effect if there are different functional groups are attached to the carbon attached to the primary carbon other than the ketone carbon?
the oc goat
very well explained. tysm!
You action love🎉
شرحك جميل😔❤
I came for the thumbnail. I want to know how that ring expansions happens.
@natsuuwu9290 check out ruclips.net/video/UE7X0pySAgE/видео.htmlsi=AYAdkEequ2xrai4-&t=1185
Here are the associated worksheet + written solutions:
worksheets.joechem.io/worksheets/Predicting%20the%20Product%20of%20Reactions%20of%20Carbonyls.pdf
worksheets.joechem.io/worksheets/Answer-%20Carbonyl%20Reaction%20Problems.pdf
Sosososososo nice
he's so hot omg
Man ur tricks of adding oxygen between 2 carbon was easy but u r speaking really fast that's getting a bit towards a volatile memory be slow have some patience teacher