BRO, you're the ONLY guy who goes over the REVERSE reaction. What a beast. What a man. What a champion of the downtrodden fools and beggars. You, sir, are elite. Love you, in the most brotherly way possible. What a guy. MashaAllah. May Allah bless this guy and increase him in EVERYTHING! lol

This helped me sooo much, especially because you are one of the only people actually showing the reverse reaction! Thank you!!

@jOeCHEM

4 жыл бұрын

someonelolxD thank you for watching 🙂 make sure to checkout the videos on my actual website joechem.io because I have worksheets with solutions posted for each video! Also, if you’d subscribe to my channel, I’d massively appreciate it 🤘🏻

I just wanna say that, even though it might have seemed insignificant to you, you speaking about how the partial positive charge being next to an ACTUAL positive charge is not good FINALLY MADE ME UNDERSTAND the basic concept that makes me realize how/why so many of these organic chemistry reactions are just ways the molecule avoids having 2 positive charges next to each other!!!! It finally made everything I have ever learned click and it really has to do with your patient method of teaching where you explained it step by step in order to have the concept make sense to ANYONE. You're the best.

You are seriously the best! I'm so glad I stumbled across your channel because I was literally dying over this chapter and you are breaking everything down so well and thank you for doing the reactions in reverse! Sooooooooo, sooooo helpful !

Thanks for rescuing me on acetal formation, you really do a great job. .

thank you!! i was confused on the reverse reaction and this video really helped me out :D

Thank you jOeCHEM.

Thank you for this.

I had a quiz today and you came in clutch.

@jOeCHEM

3 жыл бұрын

Dave! Thanks for watching, and I'm glad the video was helpful.

Thank you for simply discussion

I didn’t know Dave Franco taught chemistry

Great vid

question: What happens if the carbonyl in the ketone is attached to another carbon that is double bonded, like an alkene? Would we get the same reaction here, or would it try to attach itself to the beta carbon (1,4 conj. add. instead of 1,2 add.) and not interfere with the O = bond?

@jOeCHEM

3 жыл бұрын

Hi Junk Account (and thanks for watching)! Yeah, I think to actually get an idea of what would happen, you would have to do the experiment in real life. I imagine you would have both acetal formation (assuming you have the acidic environment necessary) as well as some 1,4 addition product.

life saver ❤

@jOeCHEM

3 жыл бұрын

Mystic Cocoa, glad you found it helpful! Thanks for watching :)

bruh ur channel underrated

@jOeCHEM

3 жыл бұрын

bruh, thank you for the kind words

question: some people online say that there is an SN1 reaction during the acetal formation after the hemiacetal was formed, where the water leaves on its own. Or is your method the right way?

@jOeCHEM

5 ай бұрын

Hi there! So I would say that me showing the double bond swing down and eject the water can also be explained as the water leaving, creating the carbocation, and then the double bond swinging down to create a resonance form. So I wouldn't even say the method I showed in this video is different than what you've explained, because whether the double bond "ejects" the water and gets formed as the water leaves, or you have the Sn1 way where water leaves and forms the carbocation, you just have 2 different resonance forms of the same molecule (hopefully that made sense, i know that was a big run on sentence).

@711Slurpies

5 ай бұрын

@@jOeCHEM no it makes A LOT of sense! So both are correct and show the concept similarly! //Quick follow up: so DOES water leave on its own as a leaving group in any other case? Or is that just a way to understand the concept?

@amanitaocreata4401

Ай бұрын

​@@jOeCHEMgreat! Thank you!

ily

🔥🔥🔥🔥🔥🔥

crazy