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Groups, Olefins, and Aromatic Hydrocarbons

Similar synergism is observed for other Br0nsted acids (FL4) in the presence of unsaturated carbon centers  [Pg.456]

For aromatic hydrocarbons, the more extensive the conjugation, the less negative the potential for direct electron transfer  [Pg.456]

The hydrolysis of carbonyl centers yields acidic hydrogens that can be reduced at platinum electrodes, for instance [Pg.456]

Likewise, the enolized form of ketones is a Br0nsted acid that can be reduced at a platinum electrode  [Pg.456]

In both cases, the reduction potential is directly related to the Br0nsted acidity, which depends on the basicity of the solvent [e.g, phenol (PhOH) has a pjfa of 16 in MeCN and 21 in Me2SO see Chapter 8]. [Pg.456]


See other pages where Groups, Olefins, and Aromatic Hydrocarbons is mentioned: [Pg.455]    [Pg.112]   


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