Which of the above compound is most reactive
towards an electrophile (E+)?
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Answered by
0
Answer:
1
Explanation:
It is most acidic.If its conjugated base is formed resonance provides stability to the compound.
Answered by
0
Answer:
1
Explanation:
For an electrophile to attack on any target molecule...that molecule must have a good electron density.
So in all four options, benzene ring of first option has conjugated bond pair from upper side chain...and also alkyl chain from lower side having +I efect on benzene...
all these two factors are increasing -ve density on benzene.
Hence 1 should be correct answer.
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