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Chemical Properties of Aromatic Nitro Compounds - Electrophilic substitution
Because - NO2 group is deactivating and m-directing, electrophilic substitution (halogenation, nitration and sulphonation) in simple aromatic nitro compounds (for example nitrobenzene) is extremely difficult as compared to that in benzene. Therefore vigorous reaction conditions are utilized for such reaction and the new group enters the m-position.
Ethylbenzene Ethylbenzene has a three-proton triplet and, at somewhat greater chemical shift, in the benzylic proton region, a two-proton quartet. p-Xylene has a six-proton si
Most ligands have a nonbonding electron pair that may react as a donor to empty orbitals on the metal atom. In ligands known as π acids or π acceptors a donor-acceptor communic
Trans -Isomer of a substance is more stable than Cis-Isomer.
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Which statement is not correct for n=5, m=3: (1) l=4 (2) l=0, 1.3, s =+1/2 (3) l= 3 (4) All are correct Ans:l=4
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