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dc.contributor.authorBaldwin, Roy R.-
dc.contributor.authorEvans, Geoffrey A.-
dc.contributor.authorWalker, Raymond W.-
dc.date.accessioned2025-04-09T10:54:29Z-
dc.date.available2025-04-09T10:54:29Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18599-
dc.description.abstractIn the presence of O2, the decomposition of 2,2,3,3-tetramethylbutane (TMB) gives 98 % of isobutene in the temperature range 420–540°C through reactions (4) and (5). (CH3)3 CC(CH3)3= 2(CH3)3C (4). (CH3)3C + O2=(CH3)2C[double bond, length as m-dash]CH2+ HO2(5). Approximately 1 % of isobutane is also obtained, and the rate of isobutane formation at a given temperature is directly proportional to [TMB], and is independent of [O2], N2 addition, and vessel diameter. It is shown that these results require the molecular reaction (3). (CH3)3 CC(CH3)3=(CH3)3 CH +(CH3)2 C[double bond, length as m-dash]CH2(3). Studies over the range 420–540°C give log10(A3/s– 1)= 13.89 ± 0.10, E3= 275 ± 1.4 kJ mol– 1. The A factor is consistent with a four-centre transition state.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (05)en_US
dc.subjectChemistryen_US
dc.subjectMolecular Decompositionen_US
dc.subjectTetramethylbutaneen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleMolecular Decomposition of 2,2,3,3-Tetramethylbutaneen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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