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dc.contributor.authorFrey, Henry M.-
dc.contributor.authorMautner, Gillian N.-
dc.date.accessioned2025-06-25T07:00:07Z-
dc.date.available2025-06-25T07:00:07Z-
dc.date.issued1974-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19005-
dc.description.abstractThe photochemical decomposition of cyclohcptanonc lias been studied in the gas phase as a function of pressure, temperature and wavelength. The major products arc carbon monoxide, hcx-l-cnc, cyclohexane and hcpt-6-enal. Quantum yields of the hydrocarbons and aldehyde were determined at 313 nm and 100'C over a range of ketone pressures. The results indicate that the hydrocarbons have a common precursor and that they arc produced by a higher energy pathway than the aldehyde. A mechanism involving a triplet state intermediate is suggested.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (07)en_US
dc.subjectChemistryen_US
dc.subjectPhotolysisen_US
dc.subjectCycloheptanonen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titlePhotolysis of Cycloheptanonen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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