A very beautiful and interesting explanation. I am a student at the College of Pharmacy, University of Baghdad. I have been following you for a while, and I was very impressed by your wonderful explanation.
Awesome video, Chad! Will you get a product for the top 4 EAS reactions even if NO2 is present? My understanding is that the only time NO2 will interfere is if it is Cl-R, or R-O-Cl (the bottom 2 reactions) Thanks!
Hey Abby - do you mean will nitrobenzene still react? It does but will direct the addition of the new substituent to the meta position due to ring deactivation - did you check out this video ua-cam.com/video/K05bDJMVgUI/v-deo.html on reactions of substituted benzene?
A very beautiful and interesting explanation. I am a student at the College of Pharmacy, University of Baghdad. I have been following you for a while, and I was very impressed by your wonderful explanation.
Glad to hear and Thank You.
@@ChadsPrep ♥️♥️♥️
Thank you all the way from South Africa. I am doing chemical engineering and you're the best!
You're welcome and Thanks from USA!
THANK YOU ALL THE WAY FROM ZAMBIA.
You're welcome from USA!
thanks alot from Egypt 🇪🇬 ❤
Very welcome from USA.
This is extremely useful! Thank you for such a great explanation!
You're welcome!
Nicely explained
Thank you 🙂
Thank you so much... From Pakistan 🇵🇰
You're welcome from USA.
Thank you so much sir .......🎉🙏🏻
And where are you from
Ty!
Welcome!
Awesome video. Thanks alot
Glad you liked it, Minh - thanks for commenting!
Thank you 🙏🏾
Very welcome.
Great Video!!
Thank you!
I like the way you say Koch
Happy Studying!
Instead of Chorine, could you use Bromine (with FeBr3) to carry out Friedel Craft Alkylation?
You totally could Joe!
@@ChadsPrep Thanks for the quick reply, Chad!
You're welcome Joe! And I will get back to you soon regarding your Biochem post :)
Awesome video, Chad! Will you get a product for the top 4 EAS reactions even if NO2 is present? My understanding is that the only time NO2 will interfere is if it is Cl-R, or R-O-Cl (the bottom 2 reactions) Thanks!
Hey Abby - do you mean will nitrobenzene still react? It does but will direct the addition of the new substituent to the meta position due to ring deactivation - did you check out this video ua-cam.com/video/K05bDJMVgUI/v-deo.html on reactions of substituted benzene?
If I have a akyl chloride, can it react with FeBr3?
Yes since it’s a halogen
I'm not quite grasping this concept at all 😩
What are you struggling with?