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In organic chemistry, a deactivating group is a functional group attached to a benzene molecule that removes electron density from the benzene ring, making electrophilic aromatic substitution reactions slower and more complex relative to benzene. Depending on their relative strengths, deactivating groups also determine the positions (relative to themselves) on the benzene ring where substitutions must take place; this property is therefore important in processes of organic synthesis.
Additional recommended knowledge
Deactivating groups are generally sorted into three categories. Weakly deactivating groups direct electrophiles to attack the benzene molecule at the ortho- and para- positions, while strongly and moderately deactivating groups direct attacks to the meta- position. This is not a case of favouring the meta- position like para- and ortho- directing functional groups, but rather disfavouring the para- and ortho- positions more than they disfavour the meta- position.
Strongly Deactivating Groups
-NO2, nitro groups
-CF3, CCl3 trihalides
Moderately Deactivating Groups
-CN cyano groups
-CO2H, -CO2R carboxylic acids
-COH, -COR alcohols and ethers
Weakly Deactivating Groups
While steric effects are a consideration not to be ignored the major contribution of deactivating groups is achieved by utilizing the nature of conjugated systems (specifically the ease through which mesomeric effects travel through such systems) to create regions of positive charge within the resonance contributors. Take for example a benzene with a nitro group substituent, the mechanistic explanation of the resulting deactivation is best explained diagrammatically:
The resulting resonance hybrid, now possessing δ+ charges in the ortho- and para- positions repels approaching electrophiles increasing the relative success of attack in the meta position.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Deactivating_groups". A list of authors is available in Wikipedia.|