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Carboxyl groups resonance energy

Data for acetic acid and eight other monobasic acids lead to a value of 1.20 v.e. for the resonance energy of the carboxyl group relative to the OH... [Pg.133]

Extra resonance energy, not including that within the benzene ring or the carboxyl group. [Pg.198]

The idea is that resonance is only possible when the proton has been lost, and that the lower energy of the resonating structure provides the driving force for the loss of the proton, and thus is the source of the acidity carboxylic group. [Pg.21]

See other pages where Carboxyl groups resonance energy is mentioned: [Pg.133]    [Pg.133]    [Pg.331]    [Pg.71]    [Pg.141]    [Pg.276]    [Pg.277]    [Pg.910]    [Pg.967]    [Pg.967]    [Pg.239]    [Pg.106]    [Pg.141]    [Pg.11]    [Pg.116]    [Pg.324]    [Pg.15]    [Pg.54]    [Pg.54]    [Pg.219]    [Pg.222]    [Pg.230]    [Pg.33]    [Pg.33]    [Pg.696]    [Pg.175]    [Pg.164]    [Pg.179]    [Pg.182]    [Pg.1701]    [Pg.193]    [Pg.271]    [Pg.274]    [Pg.274]    [Pg.69]    [Pg.341]    [Pg.1241]    [Pg.166]    [Pg.36]    [Pg.18]    [Pg.289]    [Pg.6]    [Pg.297]    [Pg.100]    [Pg.160]    [Pg.754]    [Pg.249]   
See also in sourсe #XX -- [ Pg.299 , Pg.967 ]

See also in sourсe #XX -- [ Pg.299 ]

See also in sourсe #XX -- [ Pg.299 , Pg.967 ]

See also in sourсe #XX -- [ Pg.299 , Pg.967 ]



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Carboxyl groups resonance

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Energy groups

Energy resonant

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