Bromo
substituted benzene is preferentially more reactive than Nitro substituted
benzene hence it would preferentially undergo alkylation if il is used as a solvent.On the other hand, in nitrobenzene is so strongly deactivating that nitrobenzene
does not undergo Friedel Craft reaction.
Related Questions:
Is Benzene same as 1,3,5-Cyclohexatriene ?
Which halogen best delocalises electron density to benzene ring?
Nitrobenzene and not benzene, is used as a solvent for Friedel Craft alkylation of bromobenzene. Why ?
Why tetraalkylammonium ion ((CH3)4 N+) is neither an electrophile nor a nucleophile and H3O+ is not nucleophile but electrophile although it contains a lone pair of electrons.
Why does not carbon form C+4 or C-4 ions? Explain.
Which halogen best delocalises electron density to benzene ring ?
What is Lindlar’s catalyst and does Lindlar’s catalyst use ?
Fluorine is more electronegative than chlorine even then, p-flurobenzoic acid is weaker acid than p-chlorobenzoic acid explain ?
Related Questions:
Is Benzene same as 1,3,5-Cyclohexatriene ?
Which halogen best delocalises electron density to benzene ring?
Nitrobenzene and not benzene, is used as a solvent for Friedel Craft alkylation of bromobenzene. Why ?
Why tetraalkylammonium ion ((CH3)4 N+) is neither an electrophile nor a nucleophile and H3O+ is not nucleophile but electrophile although it contains a lone pair of electrons.
Why does not carbon form C+4 or C-4 ions? Explain.
Which halogen best delocalises electron density to benzene ring ?
What is Lindlar’s catalyst and does Lindlar’s catalyst use ?
Fluorine is more electronegative than chlorine even then, p-flurobenzoic acid is weaker acid than p-chlorobenzoic acid explain ?
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