The Catalytic Isomerization of Butene-1
It has been shown that butene-1 undergoes isomerization to butene-2 on a nickel catalyst in the presence of hydrogen. By using deuterium, this double-bond migration has been examined simultaneously with the exchange and hydrogenation reactions. The kinetics of double-bond migration and hydrogenation...
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Veröffentlicht in: | Proceedings of the Royal Society of London. Series A, Mathematical and physical sciences Mathematical and physical sciences, 1941-05, Vol.178 (972), p.106-117 |
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Zusammenfassung: | It has been shown that butene-1 undergoes isomerization to butene-2 on a nickel catalyst in the presence of hydrogen. By using
deuterium, this double-bond migration has been examined simultaneously with the exchange and hydrogenation reactions. The
kinetics of double-bond migration and hydrogenation at 65$^{\circ} $C were found to be identical, the rate of reaction in
both cases being proportional to the square root of the butene pressure and to the square root of the hydrogen pressure. Energies
of activation for the three reactions were measured over the temperature range 76-126$^{\circ} $C and the following values
found: Exchange 9$\cdot $0 kcal. Hydrogenation 2$\cdot $5 kcal. Double-bond migration 5$\cdot $9 kcal. At the lowest temperatures,
the rate of double-bond migration was about six times that of exchange. These facts are in agreement with the theory that
the catalytic exchange between olefines and deuterium takes place through the formation of an associative complex. The rate-determining
step in the double-bond migration is the second, fast step of the exchange reaction, viz. $ \matrix\format\l \\ \text{CH}_{2}
\chembond{1,0} \text{CH} \chembond{1,0} \text{CH}_{2} \chembond{1,0} \text{CH}_{3}\quad \text{D}\quad \quad \text{CH}_{2}\text{D}
\chembond{1,0} \text{CH} \chembond{1,0} \text{CH}_{2} \chembond{1,0} \text{CH}_{3}\quad \quad \text{CH}_{2}\text{D} \chembond{1,0}
\text{CH} \chembond{1,0} \text{CH} \chembond{1,0} \text{CH}_{3}\quad \text{H} \\ \ \Big|\quad \quad \ \ \Big|\quad \quad \quad
\quad \quad \quad \ \ \ +\Big|\quad \rightleftarrows \quad \quad \quad \quad \Big|\quad \quad \ \ \quad \quad \quad \quad
\quad \rightleftarrows \quad \ \quad \quad \quad \Big|\quad \quad \ \Big|\quad \quad \quad \quad +\Big| \\ \text{Ni}\quad
\quad \text{Ni}\quad \quad \quad \quad \quad \quad \quad \ \ \text{Ni}\ \quad \quad \quad \quad \quad \ \,\text{Ni}\quad \quad
\quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \ \ \text{Ni}\ \,\quad \text{Ni}\quad \quad \quad \ \,\quad \text{Ni}
\\ \ \quad \quad \quad \quad \quad \quad \text{Butene-}1\quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad
\quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \text{Butene-}2 \endmatrix $ |
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ISSN: | 1364-5021 0080-4630 1471-2946 |
DOI: | 10.1098/rspa.1941.0047 |