This Thanksgiving I am thankful for Chad and his musical mnemonics.

Chad thank you so much, for having such organized, well-structured videos. These make me feel so confident in organic chemistry and really carry me throughout the units. :) You make hard concepts seem so simple!!

someone get this man an award!!!!!

I used to love organic chemistry so much in high school, but my (real-life) organic chef professor is doing a terrible job. I've been studying organic chemistry with you for almost a month now, and you are making me ENJOY the beauty of organic chemistry all over again. Even sometimes my subconscious thinks that you're my real professor because I follow with you more than I do with the "real one" XD. Thanks a lot prof. Chad!

I ACTUALLY DO GET OUT MUCH!!! THANK U VERY MUCH, CHAD

Chad, a year ago you saved me from failing my General Chemistry course, and this year I hope the same will happen with Organic Chemistry! You are the best in terms of science explanation. Thanks for what you are doing!

when the wizard is also a bard

thank you for making these videos available for everyone

Chad, you are a real God send. thank you

I was recommended your videos by another student and man, I'm impressed! These reactions gave me so much trouble since I missed out on the lectures and my professor is a bit all over the place so her explanations are a bit wonky (she's amazing but a bit inexperienced unfortunately). I'm finally understand what's actually going on! And I do have a final soon and I'm actually confident I'm gonna pass! Thank you for doing these!

Thank you for the great content! I have my exam tomorrow and your videos have been really helpful! If I get an A its because of you. 😆😊

You are amazing teacher! Thank you so much for making this it helps me a lot!

Simply masterful! Thanks Chad

I love the song it's a hit

Super sir excellent explanation, iam from India ❤

Sn2 backside attack, sn1 carbocation! 🤩I will always remember them.🤩

Excellent video. Congrats.

05:55 Wouldn't it be better for the bromide ion to deprotonate that oxonium? It is negatively charged, while the solvent (methanol) has no charge. Taking the proton would give it a positive charge, which I don't think it's willing to have. I mean, sure, the solvent may intermediate in carrying that proton from one molecule to another, but eventually, shouldn't it end up on the negatively-charged bromide and stick there to neutralize all the charges?

Thank you so much 😻❤️you really are a life saver

i'm literally only passing thanks to you lol thanks

why fluoride is a good nucleophile in polar aprotic solvent? as we know the negative charge is stable on highly electronegativeatom.shouldnot iodine be good nucleophile due to high polarazibity.

Thank you! you are amazing!

I thought more substituted carbocations would be more stable and therefore lower in energy (also more substituted is favored). Why is it at 15:27 you mention that the carbocation is higher in energy and less stable?

At 20:05 does the product have an internal plane of symmetry therefore its achiral? Or just bc its the same around the ring

omg your song is stuck on my mind loll

in 19:52 , isn't the product of proton transfer produce CH2? Not CH3?

i wish i had u as a professor

Best song ever

21:09 For this part do we need to show the substituents as a wedge or dash? Or is it okay to write them in a flat position?

Why does the nitrate ion of the AgNO3 not perform as a nucleophil?

why in the major product do we add a OCH3 instead of just OH?

that vacation joke really feels hurt

I will never forget the song🫡