Why methyl benzene/is more reactive than ethyl benzene towars electrophilic aromatic substitution?
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Answered by
11
Hey,
It is because methyl benzene has 3 hyper conjugative hydrogens whereas ethylbenzene has only 2 hyper conjugative hydrogens.
These hyperconjugations make the benzene ring more stable towards ortho-para electrophilic aromatic substitutions.....
From attachment, it is clear from the picture that the electron density is increased in the ortho and para position of benzene ring by hyperconjugation..
=========================M
It is because methyl benzene has 3 hyper conjugative hydrogens whereas ethylbenzene has only 2 hyper conjugative hydrogens.
These hyperconjugations make the benzene ring more stable towards ortho-para electrophilic aromatic substitutions.....
From attachment, it is clear from the picture that the electron density is increased in the ortho and para position of benzene ring by hyperconjugation..
=========================M
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Answered by
0
Answer:
methyl benzene
Explanation:
for electro philic substitution...
more hyperconjugative structure have more electrophilic
in case of nucleophilic.. less hyper conjugative has more nucleophilic substitution..
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