You're very welcome! Glad you found this lesson useful! I'll actually be re-filming the entire organic playlist using a whiteboard and releasing them throughout the school year. Happy Studying!
You know I love your videos and teaching style. In addition to the lecture style videos that you have, I wish you also had videos that presented a practice problem, we could pause the video, and then you could walk us through the answer. Just a thought. Thank you very much for your contribution to so many of our educations.
Ive just found this channel 🥴 it was 1hour before the test and I really think ive leant a a lot and I will come back again to this video and same comment when ive finished writing ......
@@ChadsPrep thank you very much for the 1st time in 3 consecutive tests that I've written I finally managed to get 70 % can't thank you enough but thank you😘
Chad, you're such a blessing! I find it hard to sit in the classroom and focus all throughout the 3 hr lecture so looking back at your videos really help🤧🤧 if I get an A in Ochem, its all you
At 34:00, what is stopping the water molecule from attacking the carbocation directly instead of grabbing some random protons? Isn't the positive charge on the carbocation more attractive than some neutral hydrogens? I find it a bit suspicious, because when water grabs that proton, it becomes positively charged itself, as a hydronium ion, so we're producing quite a strong acid (positively -charged) in a reaction involving a base (sure, a weak base, but still a base). Moreover, we have an even stronger base floating around - the bromide ions, which are still negatively-charged after they left the molecule. Wouldn't a bromide ion be a better candidate to take off that proton? :q
Amine leaving group (and amines are moderate bases and so poor leaving groups). I have a video regarding the Hofmann Elimination, the reaction that bears his name, here: www.chadsprep.com/chads-organic-chemistry-videos/hofmann-elimination-cope-elimination/ 😊
I find it incredibly triggering that E Z and not switched... I mean the letters could easily represent what the are with E and Z. the letter Z is clearly trans and E is clearly cis.This is why life is hard right here. Because people do stupid stuff like this... thankfully I'm ALWAYS going to remember it now lol
As someone who enjoys learning chemistry on my own these videos really are a blessing. I'm looking forward to the rest of your content :)
Glad you are enjoying it - Happy Studying!
Chad, Thank you so much!
You really help so many students do well on these difficult courses.
You'r a LEGEND!!!! THANK YOU!!
You're very welcome! Glad you found this lesson useful! I'll actually be re-filming the entire organic playlist using a whiteboard and releasing them throughout the school year. Happy Studying!
got a midterm in 2 days and I haven't practiced anything since I didn't understand the concept but I found chads video and it all makes sense now!!!!
Excellent - I hope you do well!
big test on Tuesday. this video coming in clutch for me!!!
All the best!
love your video, respect from China! You make organic fun and easy to understand.
Glad you like them, Anna!
Great presentation my man. I really appreciate the lecture.
Glad you liked it Peter!
You know I love your videos and teaching style. In addition to the lecture style videos that you have, I wish you also had videos that presented a practice problem, we could pause the video, and then you could walk us through the answer. Just a thought. Thank you very much for your contribution to so many of our educations.
Thanks for the feedback, you can always pause the videos at each example reaction I give here and see if you can figure it out before watching :)
YOU ARE AMAZING! Thanks for saving my O-Chem grade!
Glad the channel is helping you!
Ive just found this channel 🥴 it was 1hour before the test and I really think ive leant a a lot and I will come back again to this video and same comment when ive finished writing ......
Glad you found us - hope you did well on the test.
@@ChadsPrep thank you very much for the 1st time in 3 consecutive tests that I've written I finally managed to get 70 % can't thank you enough but thank you😘
@@ATM_GAMINGTOUR Glad to hear it!
Big thanks from Belgium!
A big you're welcome from the U.S., Maxime - Happy Studying!
Your be still shirt is the best! Thank you for the knowledge!
You're welcome, and thank you!
You're really good at this
Thanks for saying so, Jason!
Chad, you're such a blessing! I find it hard to sit in the classroom and focus all throughout the 3 hr lecture so looking back at your videos really help🤧🤧 if I get an A in Ochem, its all you
Thanks for saying so, Rania - hope you do well in Ochem.
Thank you chad for this video.
Very welcome
@@ChadsPrep About to go to class and learn about E1 and E2 you are the goat hopefully i'll be solving these problems before my prof does :)
@@TommyPeacock-d3b Hope it goes well!
@ 20:08 you redrew the z isomer without a wedge on the benzene ring as the final product why is that? i thought when we rotate we keep the wedge?
At 34:00, what is stopping the water molecule from attacking the carbocation directly instead of grabbing some random protons? Isn't the positive charge on the carbocation more attractive than some neutral hydrogens? I find it a bit suspicious, because when water grabs that proton, it becomes positively charged itself, as a hydronium ion, so we're producing quite a strong acid (positively -charged) in a reaction involving a base (sure, a weak base, but still a base). Moreover, we have an even stronger base floating around - the bromide ions, which are still negatively-charged after they left the molecule. Wouldn't a bromide ion be a better candidate to take off that proton? :q
HBr is a strong acid. Therefore Br(-) is a weak base.
Chad I will be offended if I dont subscribe to you. Thank u for these
You're welcome, Daniel - thanks for subscribing!
What was the bad leaving group that Hofmann worked with ?
Amine leaving group (and amines are moderate bases and so poor leaving groups). I have a video regarding the Hofmann Elimination, the reaction that bears his name, here: www.chadsprep.com/chads-organic-chemistry-videos/hofmann-elimination-cope-elimination/ 😊
Hi at 23:00 why is it hofmann instead of zaistev. In cases of Antiperiplanar would we use Hofmann?
Chad,
Thank you, so much for your awesome videos! They have helped me so much.
You're welcome, Rose - glad to hear it!
I really appreciate your work.
Excellent!
You’re a blessing!!! Thank you
Sir. You look like SAITAMA from One Punch Man
Thank you very much , wonderful explanation.
You are welcome!
Just know, i just subscribed.
Thank you!
Thank you sooooo much 😊
Yoooou're Welcome!
Thank u so much sir.
You are welcome, Alma - thanks for your comment.
you are the BEST! Thank you
Thank you so much, negar - You're welcome!
love ur vid. helps me a lot
Glad to hear it, Irfan - Happy Studying!
I love your videos!
Glad you do, Kubensis -thanks for commenting!
Maybe I'm just dumb , what the hell !!??
ur a hero
Thanks!
can you come and teach at CSUN, our chem department sucks.... "read the book" they say!
Sorry to hear of your challenges, Insha Neupane - glad the videos are helping.
I find it incredibly triggering that E Z and not switched... I mean the letters could easily represent what the are with E and Z. the letter Z is clearly trans and E is clearly cis.This is why life is hard right here. Because people do stupid stuff like this... thankfully I'm ALWAYS going to remember it now lol
Glad to hear the channel is helping you - Happy Studying!
Watching this on 1.5x
That's a great option - whatever helps you to learn, right? Happy Studying!
Can u explain this in hindi 🤣🤣🤣🤣🤣
😝 😝 😝 😝 😝 Not a chance!