I've learned that AlCl3 is not regenerated anf forms some sort of bond with the end product and is not regenerated. So it's can't be just in catalytic quantities. Which is different from the alkylation. Why is noone talking about that?
I bet there's a lot of substitution at every position. But it's possible there is slightly more substitution at the positions that are meta to one methyl and para to the other, due to sterics.
Professor Dave´s videos have the most annoying intro, but he really knows what he´s talking about! As one of many students struggling with organic chemistry during the corona self-study approach, I highly appreciate this. Thank you!
My god Professor Dave you posted this exactly when I covered this in lecture. U are some sort of Patron Saint of Organic Chem Students.
I don't think I can ever thank this guy enough
I have an olympiad this week prof dave and your chem videos helped a lot! I feel i can tackle it much better now! Thx so much!!
Just curious how did it go 5yrs back
Do you even understand how useful this stuff is, it is amazing.
Thanks for my most awaiting Chemistry Tutorial , Professor!
Give this man a prize. Thank you chem Jesus
The chemistry videos are the best. Thank you!
Your saving a whole semester of german chemistry students
thank you
Chemistry King
I've learned that AlCl3 is not regenerated anf forms some sort of bond with the end product and is not regenerated. So it's can't be just in catalytic quantities. Which is different from the alkylation. Why is noone talking about that?
Thanks
I like videos that i will watch before watch.
If you have o-Xylene for example where does the acyl get directed? And what stops all the carbons on the ring to react instead of just 1?
I bet there's a lot of substitution at every position. But it's possible there is slightly more substitution at the positions that are meta to one methyl and para to the other, due to sterics.
How can I determine if a structure is electron withdrawing/donating by inductive or resonance effect?
Good
Sir, what will be the reaction to hexane when chloroform and anhydrous aluminum chloride are added?
Thank you Jesus
Sir i a have a question. Why Al is partially - an Cl is partially +? Isn't Cl atom more electronegative?
aluminum is partial + but then when chlorine coordinates it gets a formal negative charge because it gains an electron domain
when phenol is treated with alkyl halides in presence of anhydrous alcl3 undergo alkylation to form alkyl substituted phenol
Sir please tell the mechanism when acid anhydride react with 2 eq of alcl3 with benzene.sir please reply...
Superb
Grazie.
Beautifulllll
Could the Al be replaced with any other element?
No it's quite specific to aluminum catalysts.
I hear your loud mouth in my head during exam. Basically that's how i pass. You make i lot of noise and i keep hearing your voice in exam hall, lol
Sir can activation energy be zero?
nope!
Sir do atoms react only with atoms and ions with only ions in a chemical reaction?
well ions are atoms, but no, ions and neutral atoms can react with one another.
Could you please give me an example sir
check out my clip on oxidation-reduction reactions in the general chemistry playlist
I saw it just now sir thanks a lot
Professor Dave´s videos have the most annoying intro, but he really knows what he´s talking about! As one of many students struggling with organic chemistry during the corona self-study approach, I highly appreciate this. Thank you!
Blasphemy! The intro is the best there is!^^
Thanks from algeria
ily bye
شرحك كتير حلو بس مش كلشي بفهم لانك مش حاطط ترجمة عربي لو سمحت لو بتقدر تترجمو عربي عشان نفهم
how to know its a meta director?
check out my tutorial on o/m/p directing groups it is very thorough!
@@ProfessorDaveExplains thanks prof
Hi Jesus
Kai pan kadat nahi
You seem like a pretty sick guy!
uh... thanks?
@@ProfessorDaveExplains I mean sick in a good way!
ah! well then yes, thanks :)
👍👍👍😊😊
Hello
Sir please speak in Hind
@Professor Dave Explains .. Please do a live stream suiting IST(Indian Standard Time) for your audience in India..We are awaiting it very much...
the second one i do i will make sure it's a good time for you guys, don't worry!
@@ProfessorDaveExplains Thank you so much Professor!