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Can anyone tell why methyl chloride does not react with napthalene?
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Can anyone tell why methyl chloride does not react with napthalene?
I think that answer should be like this that naphthalene is aromatic compound and theae doesn't give substitution rxn easily...
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Can anyone tell why methyl chloride does not react with napthalene?
Because nucleophilic substitution of the H of benzene is difficult because
(a) the pi electron cloud will repel the nucleophile
(b) it would be difficult for the ring to accommodate the -ve charge by the nucleophilie.
the presence of a strong electron withdrawing group can overcome this difficulty.
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Can anyone tell why methyl chloride does not react with napthalene?
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