Kolbe's Reaction | Electrophilic Aromatic Substitution Reactions | Organic Chemistry | Khan Academy
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- เผยแพร่เมื่อ 7 ก.พ. 2025
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Created by
Jitin Nair
Ortho hydroxybenzoic acid, the main product, is salicylic acid itself. Phenoxide ions would more willingly undergo electrophilic aromatic substitution than phenol ions would.
This video increased my interest in chemistry :)
Good job sir....
OMG voice___❤
normal hi toh hai 😭
Completely understood sir
He literally explained two of my questions with 1 video
Hey, I hope you understood the video fully. I have a doubt, at 4:48 he says the aromaticity of the ring is broken. What exactly does that mean? Please do tell me if you know
@@CNo-bx5mq the compound tried to get extra stable and because of that it lost it's aromaticity, so it will regain it by loosing hydrogen
@@CNo-bx5mqa molecule needs to be cyclic, planar, fully conjugated and must have 4n+2 pi electrons in order to be aromatic. with the reaction we break the conjugation (the double single double bond in that order) hence the aromaticity is broken. aromatic molecules are more stable than non-aro or anti-aro so it'll want to regain it's aromaticity
Thank sir
Sir can you plz explain Reiner Riemann reaction
Have you completed the syllabus? Just asking because jee is just weeks away.
Yes bro
My inorganic is little weak , besides that everything is covered
Where does Na+ goes in mechanism after phenoxide reacts with CO2
Third step in acid hydrolysis so NaOH regenerate
Thank you
♥️♥️
I see . Thx