Concerning in 2-methylphenol and its derivatives. A proximate coupling
Author(s) -
Ted Schaefer,
Timothy A. Wildman,
Rudy Sebastian
Publication year - 1985
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/v85-127
Subject(s) - chemistry , coupling (piping) , phenol , orientation (vector space) , group (periodic table) , spin (aerodynamics) , computation , stereochemistry , computational chemistry , medicinal chemistry , organic chemistry , geometry , thermodynamics , physics , mechanical engineering , mathematics , engineering , algorithm , computer science
In 2-chloro-6-methylphenol in CCl 4 solution, [Formula: see text] the spin–spin coupling between the hydroxyl and methyl protons, is + 68(3) mHz. In this compound, the hydroxyl group lies trans to the methyl group. If the coupling becomes −120 ± 60 mHz in a cis orientation of these two groups, then the apparent vanishing of [Formula: see text] in some derivatives of 2-methylphenol is understandable, as well as its presence in other derivatives. Computations of this coupling imply its proximate mechanism and can rationalize its value of −220 ± 20 mHz in 2-tert-butyl-6-methylphenol. Analogies are noted with [Formula: see text] in 2-trifluoromethyl phenol and with a coupling in styrene, which also appears to vanish in certain orientations of the vinyl group.
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