You taught me about chemical bonds, Acids, formal charges etc while studying in my home country. Now I am a 2nd Year Pharmacy student, still here. Thanks a lot. COOL!

Thank you for everything!! I got sick for a couple days and it was enough to make me fall behind during the hardest part of the course. I've been working every day to catch up and it's only possible because of your videos. You're an excellent teacher and thank you for sharing your videos for free. I might end up grabbing your premium course for the rest of the semester... I just wish I had started with your premium course from the beginning of the semester!!

I’m doing my pre medical program and have come across your videos recently. Life changing videos u’ve got. Let’s get through this final stage together!!!!🙌

God bless you. That’s all I can say! You’re my savior!

thanks man, I know you probably hear it alot but these videos are really helpful and I appreciate you making them.

Nice video Please also mention the effect of electron withdrawing grp such as phenyl carbonyl group that increase the rate of reaction As transition state becomes more stable

My fave professor! So happy to have found you! I have purchased the premium bundle and it is AMAZING

You’re better than my professor! Really clear demonstration! Thanks

One of your best videos I've seen, thanks Chad!

Your an awesome teacher.. just saying.

I wish you could be my professor omg! helped me through all my chem classes

Thank you teacher .you are perfect 👌🏻🌸

Thanks so much Chad!! Really appreciate it!

I can't thank you enough, this was so much helpful🙏

You are amazing Sir!

This was great!

Sir we commonly say that a weak acid has a strong conjugate base .....as well as nucleophilic strength of a nucleophile is also decided by how much weak acid is using in the reaction ...... When we use KOH in the presence of water, major product is due to substitution reaction ......while KOH in the presence of Alcohol reaction shifts towards elimination reaction .....it means in water a good nucleophile is produced but in alcohol a good base is produced.....in both cases alcohol is slightly acidic than water ....is it the peculiar behavior or my concept about strength of base and nucleophile is wrong? Looking for your guidance thank u

Hi Chad, thanks for all you do. Quick question, what is the difference between this orgo playlist and the other one (the first video of chapter 7 in this playlist is called "7.1a introduction to sn2 reaction". Thanks!

G.O.A.T.

i love you chad

why isn’t there a SN reaction video?

Why did you not put Br or NaBr as a product?

i became a pharmacist because of you now . How can i thank you

At 7:50 you said "cut their volume in half", but you meant "cut their concentration in half"...

Trigonal planar? I think it’s more trigonal bipyramidal

i love you