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DC Field | Value | Language |
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dc.contributor.author | Maccoll, Allan | - |
dc.contributor.author | Nagra, Surgit S. | - |
dc.date.accessioned | 2025-02-13T06:15:40Z | - |
dc.date.available | 2025-02-13T06:15:40Z | - |
dc.date.issued | 1973 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17667 | - |
dc.description.abstract | The kinetics of the gas phase pyrolysis of N-t-butylacetamide have been studied in a static system over the temperature range 385–465°C. The decomposition occurs by two simultaneous, homogeneous and unimolecular processes. The major process (1) is the elimination of isobutene and the formation of acetamide; the minor process (2) is the elimination of t-butylamine and the formation of ketene. CH3CONHC(CH3)3[graphic omitted](CH3)2C[double bond, length as m-dash]CH2C + CH3CONH2(1), CH3CONHC(CH3)3[graphic omitted](CH3)3CNH2+ CH2[double bond, length as m-dash]C[double bond, length as m-dash]O. (2) The rate constant for reaction (1) in the Arrhenius form is k1= 1012.42 exp (– 51 540/RT) s–1(R in cal mol–1 K–1). The acetic acid formed by subsequent decomposition of the acetamide catalyses the formation of t-butylamine and the rate constant for this bimolecular process between 400–452°C is given by k3= 1013.56 exp (– 34 950/RT) cm3 mol–1 s–1. The transition state for reaction (1) is believed to be six-centred. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1973, 69 (6) | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Homogeneous Gas Phase Pyrolysis | en_US |
dc.subject | 7V-t-Butylacetamide | en_US |
dc.subject | Journal of the Chemical Society : Faraday Transaction - I | en_US |
dc.title | Homogeneous Gas Phase Pyrolysis of 7V-t-Butylacetamide | en_US |
dc.type | Article | en_US |
Appears in Collections: | Journal Articles (before-1995) |
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