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Resonance electron-withdrawing group

Substituents such as NOz, C=N, S02CH3, CONH2, and COOR can donate an electron pair to reaction centers such as OH, NH2, OR, and SH. In the presence of a strong-resonance electron-withdrawing group and a strong-... [Pg.146]

Resonance effects Resonance electron-withdrawing groups make the carbonyl carbon more electrophilic and increase the rate resonance electron donors make the carbonyl carbon less electrophilic and decrease the reaction rate. [Pg.805]

Memorization Task 19.6 Identifying Resonance Electron-withdrawing Groups... [Pg.351]

A group with a % bond next to an aromatic ring will be a resonance electron-withdrawing group... [Pg.351]

No ordinary EAS reactions work with very deactivated rings. As a mle of thumb, a ring is considered very deactivated if it has two resonance electron-withdrawing groups (and no resonance electron-donating groups to counterbalance this). [Pg.373]

Put a box around each resonance electron-withdrawing group on the starting materials in Model 5. [Pg.387]

Explain why NAS works well with one or more resonance electron-withdrawing groups ortho or para to the leaving group, but not when such a group is meta. [Pg.387]

Construct an explanation for why neither of the aromatic rings at right will undergo NAS even though each has two resonance electron-withdrawing groups. [Pg.388]

NMR is a valuable tool for evaluating the electron withdrawing effect of aryl substituents in potential monomers. When a resonance electron withdrawing group is present on a... [Pg.278]


See other pages where Resonance electron-withdrawing group is mentioned: [Pg.562]    [Pg.767]    [Pg.79]    [Pg.562]    [Pg.800]    [Pg.818]    [Pg.800]    [Pg.818]    [Pg.562]    [Pg.965]    [Pg.339]    [Pg.584]    [Pg.353]    [Pg.366]    [Pg.366]   
See also in sourсe #XX -- [ Pg.79 ]




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Electron withdrawers

Electron withdrawing groups

Resonance electron-withdrawing

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