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We have written the ionization of mande He acid enol as involving the hydroxyl groups trans to phenyl because the trans enol of phenylacetaldehyde is a stronger acid than the cis isomer.32 Ionization of the hydroxyl group geminai to phenyl can be ruled out because ketonization would then produce pnenylglyoxal, which is not found as a reaction product.
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This is a concentration dissociation constant, applicable at ionic strength = 0.10 M
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This is a concentration dissociation constant, applicable at ionic strength = 0.10 M.
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The slopes of buffer dilution plots for some acetic acid and biphosphate ion buffers were adjusted to compensate for the fact that the enol existed in both ionized and un-ionized forms in these solutions.
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