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Meta deactivators

Classify the substituent—ortho, para activating, ortho, para deactivating, or meta deactivating— and draw the products. [Pg.659]

The 5 on this C makes the group a meta deactivator. This compound reacts more slowiy than benzene. [Pg.659]

Vinyl halides and aryl halides are unreactive. The reaction does not occur on benzene rings substituted by meta deactivating groups or NHg groups (18.1 OB). [Pg.680]

Deactivators make the ring less reactive than benzene. There are two types of deactivators - ortho/para and meta deactivators. [Pg.252]

The answer is D. The nitro group (-NO ) is a strongly electron withdrawing group, and thus a meta deactivating group. So it favors meta substitutions the most. [Pg.434]


See other pages where Meta deactivators is mentioned: [Pg.59]    [Pg.145]    [Pg.108]    [Pg.66]    [Pg.66]    [Pg.66]    [Pg.66]    [Pg.253]    [Pg.253]    [Pg.257]    [Pg.257]    [Pg.435]    [Pg.125]    [Pg.450]    [Pg.266]    [Pg.266]   
See also in sourсe #XX -- [ Pg.659 ]




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