Hello Joe! My professor says that if you let a carboxylic acid react with an amine it will form an ammoniumsalt (RCOO-NH4) it’s only when heated that you get the RCOO-NH2, but I find this odd because why wouldn’t your technique work?
Hey, you're the coolest for watching! Also, make sure to check out my actual website joechem.io (all the videos are there) and FREE worksheets + solutions. And if you’d subscribe to my TH-cam channel, I’d be forever grateful :)
Love your videos man they are always so informative! I'm trying to make anandamide for a presentation I'm preparing for my channel. I'm trying amide formation from arachidonic acid and ethanolamine and then heating. Is there any reason this should not work?
Alex Betolaza thanks Alex! Make sure to check out joechem.io for more videos and FREE worksheets + solutions. And if you’d subscribe to my TH-cam channel I’d massively appreciate it :)
revising my entire Org 2 Course from the top to see and learn things from your perspective cos wow I never thought I'd actually understand org chem (I still won't take any more chem course after org chem 2 tho cos I've had enough of chemistry lmao)
finally someone who does mechanisms clearly with many scenarios
Man you are really awesome......your teaching technique is just lit.....you deserve a lot more subscribers than you have now
This is the first time I understand this kind of reaction mechanism explanation. Great job, sir!
That is on point. In practice, we also use DCC to get H2O out of the solution and shift the reaction to right.
Interesting and thanks. Water is usually a good leaving group. And can be removed as the azeotrope with toluene.
شكرا ايها الرائع انك ممتاز لقد فهمت منك❤
In my book it says amines + cooh make salts in room temp , what does it mean can you help me with it?
You're perfect, thank you
Briee, I'm so late on this but thank you--that is so incredibly nice of you to say!
Hello Joe! My professor says that if you let a carboxylic acid react with an amine it will form an ammoniumsalt (RCOO-NH4) it’s only when heated that you get the RCOO-NH2, but I find this odd because why wouldn’t your technique
work?
Can we do this in basic conditions?
How about under acidic conditions?
Cool video bro!
Hey, you're the coolest for watching! Also, make sure to check out my actual website joechem.io (all the videos are there) and FREE worksheets + solutions. And if you’d subscribe to my TH-cam channel, I’d be forever grateful :)
i want to be in this guys gang
Love your videos man they are always so informative! I'm trying to make anandamide for a presentation I'm preparing for my channel. I'm trying amide formation from arachidonic acid and ethanolamine and then heating. Is there any reason this should not work?
thanks bro!
Alex Betolaza thanks Alex! Make sure to check out joechem.io for more videos and FREE worksheets + solutions. And if you’d subscribe to my TH-cam channel I’d massively appreciate it :)
Your speak is not understand
revising my entire Org 2 Course from the top to see and learn things from your perspective cos wow I never thought I'd actually understand org chem
(I still won't take any more chem course after org chem 2 tho cos I've had enough of chemistry lmao)