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Volumn 119, Issue 42, 1997, Pages 10203-10212

The mandelic acid keto-enol system in aqueous solution. Generation of the enol by hydration of phenylhydroxyketene and phenylcarboxycarbene

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE DERIVATIVE; MANDELIC ACID; MANDELIC ACID DERIVATIVE; PHENYLGLYOXYLIC ACID;

EID: 0030697265     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja971774r     Document Type: Article
Times cited : (51)

References (78)
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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
    • This is a concentration dissociation constant, applicable at ionic strength = 0.10 M.
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