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Benzaldehyde, electrostatic potential resonance

One further comparison aromatic aldehydes, such as benzaldehyde, are less reactive in nucleophilic addition reactions than aliphatic aldehydes because the electron-donating resonance effect of the aromatic ring makes the carbonyl group less electrophilic. Comparing electrostatic potential maps of formaldehyde and benzaldehyde, for example, shows that the carbonyl carbon atom is less positive (less blue) in the aromatic aldehyde. [Pg.704]


See other pages where Benzaldehyde, electrostatic potential resonance is mentioned: [Pg.764]    [Pg.784]    [Pg.764]   
See also in sourсe #XX -- [ Pg.44 , Pg.521 ]

See also in sourсe #XX -- [ Pg.44 , Pg.521 ]




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Potential resonances

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