Mixed

Which is the correct order of reactivity most reactive to least reactive toward electrophilic aromatic substitution?

Which is the correct order of reactivity most reactive to least reactive toward electrophilic aromatic substitution?

Therefore, the correct order of reactivity towards electrophilic substitution is Phenol > benzene > chlorobenzene > benzoic acid.

Is anisole or toluene more reactive?

Alkyl (methyl) or hydrocarbyl substitution also lends electron density to the ring. So, tentative order of reactivity in electrophilic substitution: Nitrobenzene, acetophenone, benzene, toluene, anisole; i.e. anisole is the most reactive species under these conditions.

What is the correct order of reactivity most reactive first of pyrrole furan and thiophene towards Electrophiles?

The aromatic five-membered heterocycles all undergo electrophilic substitution, with a general reactivity order: pyrrole >> furan > thiophene > benzene.

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Is nitrobenzene more reactive than toluene?

So, electrophilic nitration is less reactive in benzoic acid than benzene as the nitro group is also an electron withdrawing group. Option D is nitrobenzene. The structure of nitrobenzene is, So, the compound which is more reactive towards electrophilic nitration is toluene.

Is nitrobenzene more reactive than anisole?

Anisole reacts with electrophiles in the electrophilic aromatic substitution reaction more quickly than benzene, which in turn reacts more quickly than nitrobenzene. Rate of reaction: Anisole > Benzene > Nitrobenzene.

Why nitrobenzene is less reactive than benzene towards electrophilic substitution reaction?

Notice that nitrobenzene is less reactive than benzene because the nitro group is a deactivating substituent. Notice also that meta-substitution reactions on nitrobenzene are faster than para-substitution reactions because the nitro group is a meta-directing group.

Which is most reactive towards electrophilic aromatic substitution reaction?

The compound which is most reactive towards the electrophilic substitution is the Methyl group. Activating groups attached to the benzene ring increase the reactivity of benzene towards electrophilic substitution.

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How do you determine reactivity on the periodic table?

Period – reactivity decreases as you go from left to right. Period – reactivity increases as you go from the left to the right. Group – reactivity decreases as you go down the group.