Nucleophilic Aromatic Substitution in organic chemistry | IIT JEE & NEET | VK Sir | ATP STAR Kota

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Nucleophilic Aromatic Substitution-Important one

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Reetam Chatterjee 9

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Incredible Explanation

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Nice explanation Sir, thank you

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Extremely helpful video

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Pl give video for reagents

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Loving osm

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Mst ji

[@Anonymous-eu3lb]

Sir, please do reply, Isn't chlorine more deactivating than fluorine actually, so should'nt chlorobenzene give SnAr more ( We have learnt that fluorobenzene is more reactive towards EAS than chlorobenzene, so should'nt the order be the opposite here?)

[@its_anushka_7_]

Due to overlapping of halogens and c like f-c it's 2p-2p but in cl-c it's 3p-2p like so on

[@ankurdudi4632]

Sir iss rxn me polar aprotic solvent use nhi krnge kya or any nucleophile Will show rxn

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Thank u so much Sir 😊

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Bole too jhakass

[@richakumari7480]

If negative charge is stabilised than how again there is -ve charge on the ortho position to regain the aromaticity ?

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Yes

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Its already there bro ..

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Dera sir, pls make a video on SN2 tetrahedral mechansism of grignard

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Best ........

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Thanks sir

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Good, but some more eg. Required in ending..

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धन्यवाद

[@YashaswiChoudhary-mt5zs]

Sir fluorine or chlorine Wale question me +ve jyada stable fluorine ke saath kyu hua?

[@sahilagrawal1522]

Why no2 not leave instead of cl group. Please ans sir

[@Sharma.2023]

NO2 is an electrophile not a neucleophile...

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Ty

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Thnq sir

[@shubhamgandhi5959]

Sir in second question will delta positive charge will be same at eipso pos?

[@diptilulla2895]

is this a possible mechanism of Dow process

[@omyadav9272]

Yes it is

[@nainaramani7383]

Sir ,can halobenzene react with oh- in extreme conditions like high pressure(about 300 atm) and high temperature(about 600K) without the presence of no2 group?

[@omyadav9272]

Yes, it undergoes dow's process

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Make a video on stereochemistry

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When π bond breaks then why positive charges do not appear as You said vallency free hota hein

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thank you sir....the method you use to explain the complete process is superb

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Woo

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Dow’s process?

[@sujaltripathi3830]

Isme sir no2 ka structure nhi samajh me rha hai ...plz btaiye sir

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😂😂😂

[@avnish5352]

Sir why chlorine gone why not OH IN LAST STEP at 5:45

[@AyushSingh-qt2fn]

Avnish Kumar prajapati becoz. Cl is better leaving group than OH

[@generax-zu9jc]

OH ko lgaya hi kyu jb nikalna hi tha !!

[@shrutirathore6000]

sir OH group is electron releasing group not a not a donating in ur video its shown at 5:40 .....sir I m confused .. plss rplyy me

[@kapildeshmukh7878]

Shruti Rathore It's the same thing. EDG and ERG (Donating and Releasing) means the same thing.

[@jyotishrivastva2089]

Kapil Deshmukh how you can say these both r same

[@lalitchaudhary187]

Only one example of snAr............

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not bad

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at least do one tough question in video

[@lordelectron6591]

Sir, I have a doubt regarding a question. What will be the end product when m-bromo nitro benzene reacts with NaNH2 in presence of Toluene?

[@amanbelim0083]

Aromatic compound gives both electrophilic and nucleophilic substitution both or not??

[@geetaraniverma1858]

Yes they both give

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very nice explanation ,thank you

[@vegetaandslaine8722]

Bhai 1:22 wale question mein Cl Ko hi kyun replace Kiya hai NO2 Ko kyun nahi Kiya

[@abhashrivastava8492]

Leaving group order: F > NO2 > Cl ≈ Br > I

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