Diazonium Salt Formation Mechanism
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- Опубликовано: 7 июл 2024
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The best vid about the diazonation reaction ! Thank you have a great day
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Crystal clear explanation about Diazotization rxn
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BEST EXPLANATION
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Thanks very much for explaining diazonium ion
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Doesn't the tertiary amino group at the end is a deactivator since Nitrogen is more electronegative than Carbon making it a meta director ?
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Sir please explain other complicated reactions in the same way while posting any other videos
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from where did base come up there?
why this reaction proceeds at very low temperature?
Fantastic..
What kind of base is used?
What does "N" indicate in N-hydroxy azo compound?
I believe it means the hydroxyl group is bonded to the nitrogen
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From where did the base come? We didn't use it in the reagents.
It's not always listed in the reagents in most textbooks, however, a base is used in this reaction. Many bases can be used.
the base could be water, that has formed and the acid would be H30+
Nice
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Sir,why use excess HCl here??
Why we use excess HCl here??
thanks
You're welcome!
what kind of acid and base is used?
I think acids with high H+ dissociation ex: HCl, H2SO4
Why doesn't NO+ do electrophilic attack on the ring ?
It does. But that's a different reaction. I cover this in another video.
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But it undergoes in 273 k to 278 Kelvin
sir what happens to na+
it leaves as nacl
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How to: Gamma-Amino-Butyric Acid + NaNO2 + HCl ^ -- Gamma Hydroxy-butyric Acid.
Thanks