at 6:55 when you drew the second resonance structure, I believe you meant to put the double bond formed by the lone pair on the two left most carbons but accidentally put it on the top carbon, making it a carbon with 5 bonds total. Just incase anyone caught that and was confused.
The reaction can occur without the EWG. If there's an EWG at the ortho/para position the reaction proceeds through the "Meisenheimer complex" intermediate. If there's no EWG the reaction can proceed through the "Benzyne" intermediate. May wanna look up these terms.
dan da yes Replaced chloride added OH group than we get Nitro phenol than make a aniline of by reduction than we will get Para hydroxy aniline than diazotise by HCl and NaNO2 at 0-5 C and earn it than I will get Phenol
Yes it does and that’s what he used for the addition elimination reaction where the chlorine is replaced with the amines group.The sodium is more like a catalyst
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at 6:55 when you drew the second resonance structure, I believe you meant to put the double bond formed by the lone pair on the two left most carbons but accidentally put it on the top carbon, making it a carbon with 5 bonds total. Just incase anyone caught that and was confused.
yes thanks so much lol I was so confused
Was bothering the hell out of me
Im on vacation and Im learning so much more watching your videos than I did on the semester, thank youuuuuuuuuuuuuu!
Iam also learning in holidays 🥺
What? You learning this in University level? Here I am facing all these organic chemistry in grade 11,India. Cheers to you mate! Have a nice day
@@MovieMania-pw7uv Bro😢
Meisenheimer? More like “Many thanks because now we’re wiser!” Your videos, and not just those on organic chemistry, are amazing.
haha so funny
@@iwanttwoscoops Hey there’s no substitution for the aroma of good humor…
Really......your vedios are awsome sir.....love from india
Love from Pakistan
Sir please make video of benzyne reactions and formation...your videos have been thirst relievers...huge respect sir!
7:00 the carbon has 5 hands isn't that wrong?
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We love you from ethiopia 🇪🇹🇪🇹
If l had EWG meta to leaving group
Will it react by addition elimination reaction
or elimination addition reaction????
You r always amazing....thank u so much
This is the beauty of Chemistry !!
Organic Chemistry is Satan's mother.
@@ronlund5291 I never knew I’d read that phrase in my life, but I do agree that ochem is really difficult!
@@PunmasterSTP agreed. Although, that is way behind me. I graduated shortly after I posted that 2 years ago 😁
@@ronlund5291 I’m glad it’s behind you! If I might ask, where’d you end up after graduating?
@@ronlund5291 are u a allenite?
Explanation SN1 using benzenedizonium chloride
Thank you...from Iraq
On benzyne intermediate, with no EWD or EDG. How could the benzyne form on the right emaide of the ring where there is no double bond?
hello sir i need help with some organic chemistry problems would you plz help me?
i will show the pdf u might have videos that would be helpful
In the last one could you tell the major product
major product would probably be the first one due to sterics
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How come you dont need an EWG for these reactions? Dont you need it for nucleophilic reaction?
The reaction can occur without the EWG. If there's an EWG at the ortho/para position the reaction proceeds through the "Meisenheimer complex" intermediate. If there's no EWG the reaction can proceed through the "Benzyne" intermediate. May wanna look up these terms.
You won't need if you have a very strong nuceleophile or base
So can you still have nuc sub at the meta position, just very little, or not at all due to the lack of stabilisation via the NO2?
What reaction would occur of the EWG is trifluoromethyl instead of the nitro group?
what exactly determines the "leaving group"
Last question what's the major product?
the para product
@@bbk9625 para to what methyl or isopropyl???
@@ToqaAfsa Isopropyl
@@ToqaAfsa meta to methyl
How i know on aroamtic, elektrophile or nukleophile SUB.
How do you know that sodium is a spectator ion?
we just do. We learnt that in gen chem.
ur mom
4;11 thats a good looking benzene!!!
Is it possible to make phenol instead of aniline?
dan da yes
Replaced chloride added OH group than we get Nitro phenol than make a aniline of by reduction than we will get Para hydroxy aniline than diazotise by HCl and NaNO2 at 0-5 C and earn it than I will get Phenol
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does chlorobenzene react with sodium amide at all ??
Yes it does and that’s what he used for the addition elimination reaction where the chlorine is replaced with the amines group.The sodium is more like a catalyst
Sir this is for benzyne mechanism?..?????
tysm
اشخري يحسنية
ur so cute ily