16.5b Stereoselectivity and Regioselectivity in Diels Alder Reactions
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- Опубліковано 10 лют 2025
- Chad breaks down how to predict the products in Diels-Alder reactions, explaining both the Stereoselctivity and Regioselectivity.
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This whole semester I avoided wasting time searching the endless videos and teaching styles on UA-cam and instead just read my textbook and tried deciphering lecture notes from my professor. I really wish I would have stumbled upon your channel beforehand. Regardless, thank you!!
Glad you found us - Happy Studying!
Perfect explanation. Exactly what I was looking for!
Fantastic!
you are my favorite channel right now
Excellent - glad you found us!
Have an exam tomorrow, and I've been searching for the explanation of the regioselectivity of electron withdrawing groups on the dienophile, and why they would somehow end up on different carbons than what seemed to be intuitive. Thank you so much for this video! I understand it completely after you've explained it. Should've known that if something gets counterintuitive, resonance is involved! Liked and subscribed
Glad you found us, Eric -thanks for the like and subscribe! Glad you were able to get the understanding you were looking for - hope you did well on your exam.
Thank you so much
You are welcome.
you are GOD SEND!! used you for gen chem and orgo 1 I am applying to med school and plan on using your MCAT prep too!!
Excellent, Wislane Noel - glad you found us!
Thanks. Clear and very well explained!
You're welcome and glad you found it helpful!😀
very helpful, Thank you :) greetings from Germany
Once again you're very welcome and greeting back from the U.S. (Arizona)!
thank you so much for the explanations and drawings, they are super helpful
You're welcome!
Saved me hours of headache, wish you were my org teacher lol!
Glad the video/channel is helping you - Happy Studying!
Thank you so much! Your video really helped me understand regioselectivity!
Glad to hear it - you're welcome!
Thanks for the explanation 🙂
You are welcome, Izar - thanks for watching!
Nice lecture! Great Work!!!
Thanks a lot Vasu! Very glad you found it helpful!
Very good sir
Thanks.
According to my theory, ethylene reacts sluggishly meaning the dienophile prefers to attach itself to an electron-withdrawing group which basically lowers the energy of the alkene double-bond electrons so they can react with the dienes. Is that the case?
Thank you Chad
thanks Chad
Thank you
You're welcome, Golcha.