00:02
Around the compounds in each group in order of their reactivity to electrotheric substitution.
00:12
A, nitrobenzym, phenol, toureen, and benzene.
00:39
So the most reactive will be phenol.
00:44
It has a strong resonance donor.
00:47
Second in reactivity would be tourine.
00:50
It's a hyperconjugative donor.
00:54
Then, benzene.
00:59
And the least reactive would be nitrobenzyme with the nitro group, which is the electron acceptor, a very strong one.
01:10
B, phenyl, chlorobenzine, and benzoic acid.
01:39
The most active will be phenol.
01:46
Chlorobenzene, it's an acceptor, inductive acceptor, resonance acceptor because of empty 3d orbital and also resonance donor because of those electrons.
02:01
But overall, it's an acceptor and it deactivates the ring.
02:08
So second in reactivity will be benzene...