16.4 Addition Reactions to Conjugated Dienes
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- Опубликовано: 26 авг 2024
- Chad breaks down Addition reactions to Conjugated Dienes differentiating between Kinetic and Thermodynamic Products and the conditions that favor them.
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Happy Studying!
What a great video. Im in o chem 2 and this video made the concept a lot less confusing, thanks!!
Glad you found it helpful Anthony!
this video is amazing. it helped understand the concept in 11 minutes!
Awesome Diana! So glad you found it helpful and efficient!
I love this part of ochem: conjugated systems and aromatics. All the background information is over with (ochem 1, lol) and you start learning applicable chemistry especially in nature.
Totally agree Zach! Glad you're enjoying it
Best as always!!
Thank you!
Thank you, Chad!
You're welcome Anthony!!!😊
excellent explanation!
Glad it was helpful, Sarah - thanks for letting us know.
awesome video !
Thanks for the visit, Alexis - and thanks for saying so!
everyone else is saying they're studying this for ochem2. Then WHY THE HECK am I learning it for ochem 1 🤧🤧🤧 ty for your help!
You're welcome!
I have a disagreement with you sir at the time 7.55 min.
Firstly, the tertiary carbocation does not bear a greater positive charge density than the primary carbocation. The tertiary carbonium ion has more alkyl groups which donate more electron density to the tertiary carbonium ion, leading to lower positive charge density.
Secondly, the 1,2 addition product (kinetic product) is a major product due to the higher concentration of tertiary carbocation ions (being more stable) in the reaction solution, since the kinetic product is not reversible.
Finally, at a high temperature (thermodynamic product), the tertiary carbocation ion would also be in a higher concentration, and initially, 1,2 addition (kinetic product) would be formed quickly but due to its less EA and instability it is reversible at a high temperature and ultimately a 1,4 addition product would be formed.
Last but not least, you are an amazing teacher! keep up the good work.