## Abstract The addition of propene to cyclohexa‐1,3‐diene has been studied between 512 and 638°K at pressures between 70 and 640 torr. The products are endo‐ and exo‐5‐methylbicyclo [2.2.2] oct‐2‐ene, and their formations are second order. The rate constants (in 1./mole‐sec) are given by The resu
Kinetics and mechanism of the addition of 1,3-butadiene to cyclohexa-1,3-diene in the gas phase
✍ Scribed by G. Huybrechts; Y. Hubin; M. Narmon; B. Van Mele
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 333 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
The thermal reactions of 1,3‐butadiene (BD) with cyclohexa‐1,3‐diene (CHD) have been studied in a static system between 437 and 526 K. The pressures of BD and CHD were varied from 61 to 397 torr and from 50 to 93 torr, respectively. The percentages of consumed BD and CHD were always kept lower than 14%. The reactions—in the order of importance—are
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All the reactions are homogeneous and of the first order with respect to the reagents. Their rate constants (in L/mol·s) are given by
A thermochemical analysis of a biradical mechanism is in agreement with these results.
📜 SIMILAR VOLUMES
## Abstract The Diels–Alder addition of acrolein to cyclohexa‐1,3‐diene has been studied between 486 and 571°K at pressures ranging from 55 to 240 torr. The products are endo‐ and exo‐5‐formylbicyclo[2.2.2]oct‐2‐ene (endo‐ and exo‐FBO), and their formations are second order. The rate constants (in
## Abstract The addition of ethene to cyclohexa‐1,3‐diene has been studied between 466 and 591 K at pressures ranging from 27 to 119 torr for ethene and 10 to 74 torr for cyclohexa‐1,3‐diene. The reaction is of the “Diels–Alder” type and leads to the formation of bicyclo[2.2.2]oct‐2‐ene. It is homo
The reactions k N n m endo-5-Ybicyclo[2.2.2loct-2-ene (NYBO) eno-5-Ybicyclo[2.2.2loct-2-ene (XYBO) O + < , < (YE) KXYBO (CHD) where Y = CH, (MI, C,H, (E), i-C,H, (I), and t-C,H, (TI have been studied between 488 and 606 K. The pressures of CHD ranged from 16 to 124 torr and those of YE from 57 to 62
The kinetics of the Diels-Alder additions of C H 2 = CHCN, CH, = C(CH3) CN, and cisand trans-CH,CH = CHCN to cyclohexa-l,3-diene have been studied in the gas phase. The stereochemistry of these reactions is discussed. In terms of a biradical mechanism, a minimum value of 4.1 5 0.8 kcal mol-' for the
The kinetics of the Diels-Alder additions of CH,= CHCHO, CH2= C(CHdCH0, and CH2= CHC(CH,)O to cyclohexa-1,3-diene (CHD) have been studied in the gas phase. The stereochemistry and the mechanism of these reactions are discussed. In contrast with other Diels-Alder additions involving CHD as diene, a b