Substituent effects on the dehydration of arene hydrates in aqueous solution

O'Mahony, Michelle J.; O’Ferrall, Rory A. More; Boyd, Derek R.; Lam, Casey M.; O’Donoghue, AnnMarie C.

doi:10.1002/poc.3174

Cited by 7 publications

(1 citation statement)

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“…The acid-catalyzed dehydration of arene dihydrodiols − and arene hydrates has been extensively studied experimentally and is generally thought to proceed through a carbocation intermediate. Recently, More-O’Ferrall provided the first evidence that, for benzene cis -1,2-dihydrodiols, this reaction also occurs under base catalysis at room temperature with aqueous sodium hydroxide .…”

Section: Introductionmentioning

confidence: 99%

Concerted or Stepwise: How Much Do Free-Energy Landscapes Tell Us about the Mechanisms of Elimination Reactions?

2014

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The base-catalyzed dehydration of benzene cis-1,2-dihydrodiols is driven by formation of an aromatic product as well as intermediates potentially stabilized by hyperaromaticity. Experiments exhibit surprising shifts in isotope effects, indicating an unusual mechanistic balance on the E2-E1cB continuum. In this study, both 1- and 2-dimensional free energy surfaces are generated for these compounds with various substituents, using density functional theory and a mixed implicit/explicit solvation model. The computational data help unravel hidden intermediates along the reaction coordinate and provide a novel conceptual framework for distinguishing between competing pathways in this and any other system with borderline reaction mechanisms.

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