7 E1 vs E2

[@chlorophyll1067]

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 :)

[@ChadsPrep]

Glad you are enjoying it - Happy Studying!

[@HZMusic613]

Chad, Thank you so much! You really help so many students do well on these difficult courses. You'r a LEGEND!!!! THANK YOU!!

[@ChadsPrep]

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!

[@peterk.4266]

Great presentation my man. I really appreciate the lecture.

[@ChadsPrep]

Glad you liked it Peter!

[@annayan6124]

love your video, respect from China! You make organic fun and easy to understand.

[@ChadsPrep]

Glad you like them, Anna!

[@demifujino1816]

YOU ARE AMAZING! Thanks for saving my O-Chem grade!

[@ChadsPrep]

Glad the channel is helping you!

[@ATM_GAMINGTOUR]

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]

Glad you found us - hope you did well on the test.

[@ATM_GAMINGTOUR]

@@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😘

[@ChadsPrep]

@@ATM_GAMINGTOUR Glad to hear it!

[@kagamer21]

Your be still shirt is the best! Thank you for the knowledge!

[@ChadsPrep]

You're welcome, and thank you!

[@maximehendrickx6212]

Big thanks from Belgium!

[@ChadsPrep]

A big you're welcome from the U.S., Maxime - Happy Studying!

[@TommyPeacock-d3b]

Thank you chad for this video.

[@ChadsPrep]

Very welcome

[@TommyPeacock-d3b]

@@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 :)

[@ChadsPrep]

@@TommyPeacock-d3b Hope it goes well!

[@trev_rose]

Chad, Thank you, so much for your awesome videos! They have helped me so much.

[@ChadsPrep]

You're welcome, Rose - glad to hear it!

[@danielchuhan6716]

Chad I will be offended if I dont subscribe to you. Thank u for these

[@ChadsPrep]

You're welcome, Daniel - thanks for subscribing!

[@bushraalsulaiman4343]

I really appreciate your work.

[@ChadsPrep]

Excellent!

[@Rania-vh7wg]

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

[@ChadsPrep]

Thanks for saying so, Rania - hope you do well in Ochem.

[@jasonqlwilliams]

You're really good at this

[@ChadsPrep]

Thanks for saying so, Jason!

[@randyoteng9313]

You’re a blessing!!! Thank you

[@elizabethibarra2761]

@ 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?

[@IshratParveen-to1xv]

Thank you sooooo much 😊

[@ChadsPrep]

Yoooou're Welcome!

[@ibnaden]

Hi at 23:00 why is it hofmann instead of zaistev. In cases of Antiperiplanar would we use Hofmann?

[@almacyrenable]

Thank u so much sir.

[@ChadsPrep]

You are welcome, Alma - thanks for your comment.

[@negarrrg]

you are the BEST! Thank you

[@ChadsPrep]

Thank you so much, negar - You're welcome!

[@bonbonpony]

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

[@simoko7076]

HBr is a strong acid. Therefore Br(-) is a weak base.

[@irfankhumaini9910]

love ur vid. helps me a lot

[@ChadsPrep]

Glad to hear it, Irfan - Happy Studying!

[@grantking4032]

Just know, i just subscribed.

[@ChadsPrep]

Thank you!

[@MrStrutxD]

I love your videos!

[@ChadsPrep]

Glad you do, Kubensis -thanks for commenting!

[@dianahasan4194]

What was the bad leaving group that Hofmann worked with ?

[@ChadsPrep]

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/ 😊

[@HomeStudiosGaming]

ur a hero

[@ChadsPrep]

Thanks!

[@inshaneupane5626]

can you come and teach at CSUN, our chem department sucks.... "read the book" they say!

[@ChadsPrep]

Sorry to hear of your challenges, Insha Neupane - glad the videos are helping.

[@ntsoakiphetla6836]

Maybe I'm just dumb , what the hell !!??

[@TheDedloc]

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

[@ChadsPrep]

Glad to hear the channel is helping you - Happy Studying!

[@dorukhanallinson6162]

Watching this on 1.5x

[@ChadsPrep]

That's a great option - whatever helps you to learn, right? Happy Studying!

[@Buchkanbhaiya3288]

Can u explain this in hindi 🤣🤣🤣🤣🤣

[@ChadsPrep]

😝 😝 😝 😝 😝 Not a chance!