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05:56
Q---
Why these two reaction forms different product(i mean one is replacing H- & other is substituting NO2) ?
CN- is better nucleophile than CH3O- still it isn't able to substitute NO2
Both reaction have same mechanism ArSN2 still different type reaction?? How Why??
@Newton right one is incorrect.
Aniruudha oops wrong fig.
@AniruddhaDeb can you delete that fig.
Q---
Why these two reaction forms different product(i mean one is replacing H- & other is substituting NO2) ?
CN- is better nucleophile than CH3O- still it isn't able to substitute NO2
Both reaction have same mechanism ArSN2 still different type reaction?? How Why??
@Newton I can't; you can though.
the only difference i can see b/w these two reaction is -CN is weaker acid than methoxide but a better nucleophile than methoxide. But still i can't find any reason behind these two different reaction
@YusufHasan
06:09
@Newton I highly doubt the first reaction will take place... ArSN needs -NO2 group at ortho/para position. The second reaction is more probable since all -NO2 groups are ortho/para and CN- is a relatively small nucleophile, so it can 'fit' in between two -NO2 groups meta to each other.
 
2 hours later…
07:52
@YusufHasan bhai ho ske toh first reaction ka mechanism bhi likh dijiye ga
my attempt
iske baad kuch samajh mein hi nii aaya
 
4 hours later…
11:39
@Newton not needed
Stick to syllabus
 
1 hour later…
12:43
In a quora post i read "When CH3 is directly attached to O(e.g. methoxide) then CH3 acts as Electron Withdrawing Group , it's also proven by NMR Spectroscopy"
Is it true ?
Link to that post -
Also one more doubt "we call CH3 an electron releasing group only when attached to an -I group "
Is it true ?
My sir taught us R is always +I (or electron releasing ) , Except in organometallics like (Grignard Reagents) .
Sir aisa kuch toh nii btaya ???
 
3 hours later…
16:10
@Newton Never heard of that

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