On the Unimolecular Decomposition of the tert-Butoxy Radical

Yip, Carol; Pritchard, H. O.

doi:10.1139/v73-321

Cited by 3 publications

(1 citation statement)

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“…This was subsequently demonstrated experimentally by several workers. However, Yip and Pritchard attribute the "apparent" observed pressure dependence to heterogeneous effects [61]. It is perhaps pertinent to point out that the low value of A 3 determined by Birss and coworkers [51] was due to an erroneously low estimation for A , of lO'M-'.s-'.…”

Section: Chs No Formationmentioning

confidence: 99%

ChemInform Abstract: THE GAS PHASE PYROLYSIS OF ALKYL NITRITES. I. T‐BUTYL NITRITE

Batt¹,

Milne²

1976

Chemischer Informationsdienst

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The rate of decomposition of t-butyl nitrite (TBN) has been studied in a static system over the temperature range of 12O-16O0C. For low concentrations of TBN (lo-" 10-4M), but with a high total pressure of CF4 (-0.9 atm) and small extents of reaction (-I%), the first-order homogeneous rates of acetone (M2K) formation are a direct measure of reaction (l), since k3>> k2 (NO): TBN 2 t-BuO + NO, t-BuO -+ MZK + Me. Addition of large amounts of NO in place of CF4 almost completely suppresses M2K formation.This shows that reaction (1) is the only route for this product. The rate of reaction From. &So1 and A,, k2 is calculated to be 1010.4M-1.~-1, implying that combination of t-BuO and NO occurs once every ten collisions. From an independent observation that k2/k2) = 1.7 =k 0.25 independent of tempera,ture, it is concluded that kt' = 101n~2hf-1~s-1 and k,' = 1015.9-40~2/6 s-l; t -B u O N O z q t-BuO + NO2. This study shows that MeNO arises solely as a re+ of the combination of Me and NO. Since NO is such an excellent radical trap for t-BuO, reaction (2) may be used in a competitive study of the decomposition of t-BuO in order to obtain the first absolute value for k3. Preliminary results show that k3 ( a ) = 1015.7-17.0/e s-,. The pressure dependence of k3 is demonstrated over the range of 10-z-l atm (ISOOC). The thermochemistry for reaction (3) implies that the H g 6(3P1) sensitised decomposition of t-BuOH occurs via reaction (m):I n addition to the products accounted for by the TBN radical split, isobutene is formed as a result of the 6-centre elimination of HONO: TBN 4 isobutene + HONO. The rate of formation of isobutene is given by k7 = 1012.9-33.6/8 s-l. t-BuOH, formed at a rate comparable to that of isobutene-at least in the initial stages-is thought to arise as a result of secondary reactions between TBN and HONO. The apparent discrepancy between this and previous studies is reconciled in terms of the above parallel reactions (1) and (7), such that k + 2k7 = 1014.'-36.2/f3 s-l.

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Section: Chs No Formationmentioning

confidence: 99%

ChemInform Abstract: THE GAS PHASE PYROLYSIS OF ALKYL NITRITES. I. T‐BUTYL NITRITE

Batt¹,

Milne²

1976

Chemischer Informationsdienst

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Zur Kinetik unverzweigter Kettenreaktionen

Scherzer

1976

Zeitschrift fuer Chemie

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The gas phase pyrolysis of alkyl nitrites. I. t‐butyl nitrite

Batt

Milne

1976

Int J of Chemical Kinetics

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The rate of decomposition of t‐butyl nitrite (TBN) has been studied in a static system over the temperature range of 120–160°C. For low concentrations of TBN (10−5‐ 10−4M), but with a high total pressure of CF4 (∼0.9 atm) and small extents of reaction (∼1%), the first‐order homogeneous rates of acetone (M2K) formation are a direct measure of reaction (1), since k3» k2 (NO): TBN . Addition of large amounts of NO in place of CF4 almost completely suppresses M2K formation. This shows that reaction (1) is the only route for this product. The rate of reaction (1) is given by k1 = 1016.3–40.3/θ s−1. Since (E1 + RT) and ΔH °1 are identical, both may be equated with D(RO‐NO) = 40.9 ± 0.8 kcal/mole and E2 = O ± 1 kcal/mole. From ΔS °1 and A1, k2 is calculated to be 1010.4M−1 ·s−1, implying that combination of tBuO and NO occurs once every ten collisions. From an independent observation that k2/k2′ = 1.7 ± 0.25 independent of temperature, it is concluded that k2′ = 1010.2M−1 · s−1 and k1′ = 1015.9−40.2/θ s−1; . This study shows that MeNO arises solely as a result of the combination of Me and NO. Since NO is such an excellent radical trap for t‐Bu\documentclass{article}\pagestyle{empty}\begin{document}${\rm Me\dot O}$\end{document}, reaction (2) may be used in a competitive study of the decomposition of tBu\documentclass{article}\pagestyle{empty}\begin{document}${\rm Me\dot O}$\end{document} in order to obtain the first absolute value for k3. Preliminary results show that k3 (∞) = 1015.7–17.0/θ s−1. The pressure dependence of k3 is demonstrated over the range of 10−2−1 atm (160°C). The thermochemistry for reaction (3) implies that the Hg 6(3P1) sensitised decomposition of t‐BuOH occurs via reaction (m): In addition to the products accounted for by the TBN radical split, isobutene is formed as a result of the 6‐centre elimination of HONO: TBN \documentclass{article}\pagestyle{empty}\begin{document}$\mathop \to \limits^7 $\end{document} isobutene + HONO. The rate of formation of isobutene is given by k7 = 1012.9–33.6/θ s−1. t‐BuOH, formed at a rate comparable to that of isobutene–at least in the initial stages–is thought to arise as a result of secondary reactions between TBN and HONO. The apparent discrepancy between this and previous studies is reconciled in terms of the above parallel reactions (1) and (7), such that k + 2k7 = 1014.7–36.2/θ s−1.

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On the Unimolecular Decomposition of the tert-Butoxy Radical

Cited by 3 publications

References 3 publications

ChemInform Abstract: THE GAS PHASE PYROLYSIS OF ALKYL NITRITES. I. T‐BUTYL NITRITE

ChemInform Abstract: THE GAS PHASE PYROLYSIS OF ALKYL NITRITES. I. T‐BUTYL NITRITE

Zur Kinetik unverzweigter Kettenreaktionen

The gas phase pyrolysis of alkyl nitrites. I. t‐butyl nitrite

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