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All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...
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Don't link carbon markets

Jessica F Green1

  • 1Department of Environmental Studies, New York University, New York City, USA.

Nature
|March 24, 2017
PubMed
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No abstract available in PubMed .

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