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dc.creatorFreedman, H. H.en_US
dc.date.accessioned2006-06-15T12:53:10Z
dc.date.available2006-06-15T12:53:10Z
dc.date.issued1958en_US
dc.identifier1958-I-10en_US
dc.identifier.urihttp://hdl.handle.net/1811/7759
dc.descriptionAuthor Institution: Eastern Research Laboratory, The Dow Chemical Companyen_US
dc.description.abstract“The relative importance of an inductive vs. a resonance mechanism for the high carbonyl absorption frequency of phenyl acetate and acetanilide has been investigated. A study of the C-O frequency shifts in their meta and para-subtituted derivatives clearly shows that the inductive mechanism is responsible for the frequency shift in phenyl acetate, but a resonance mechanism is more appropriate in the acetanilides. This is supported by a study of their respective Stuart-Briegleb molecular models which, on the basis of steric inhibition of resonance due to lack of coplanarity within the molecule, indicates that a resonance mechanism is relatively unimportant in phenyl acetate.”en_US
dc.format.extent69096 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleELECTRONIC INTERACTIONS IN PHENYL ACETATES AND ACETANILIDESen_US
dc.typearticleen_US


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