Catalysis by hydrogen halides in the gas phase. XVI. Methyl trimethylacetate, isopropanol, and hydrogen bromide

1968 ◽  
Vol 21 (3) ◽  
pp. 713 ◽  
Author(s):  
JTD Cross ◽  
VR Stimson
Keyword(s):  
Carbon Monoxide ◽  
Gas Phase ◽  
Rate Constants ◽  
Hydrogen Bromide ◽  
Hydrogen Halides ◽  
Individual Rate

In the presence of hydrogen bromide at 407�, methyl trimethylacetate decomposes to isobutene, carbon monoxide, and methanol. Isopropanol reacts with an intermediate to form isopropyl trimethylacetate, which decomposes quickly to propene. Methanol competes effectively with isopropanol. Some ratios of individual rate constants are obtained from the rate reductions in the competition reactions.

Catalysis by hydrogen halides in the gas phase. XVII. Isobutyric acid and hydrogen bromide

1968 ◽  
Vol 21 (3) ◽  
pp. 725 ◽  
Author(s):  
JTD Cross ◽  
VR Stimson
Keyword(s):  
Carbon Monoxide ◽  
Gas Phase ◽  
Rate Constants ◽  
Hydrogen Bromide ◽  
Isobutyric Acid ◽  
Kcal Mole ◽  
Hydrogen Halides ◽  
Arrhenius Parameters ◽  
First Order ◽  
Added Water

Hydrogen bromide catalyses the decomposition of isobutyric acid into propene, carbon monoxide, and water at 369-454�. Hydrogen bromide is not lost. Individual runs follow the first-order rate law, and the rate constants are proportional to the hydrogen bromide pressure. The Arrhenius parameters are: E = 33.17 kcal mole-1 and A = 1012.87 sec-1 ml mole-1, and the reaction is homogeneous and molecular. Added water or methanol retards the reaction.

Catalysis by hydrogen halides in the gas phase. XVIII. Methyl formate and hydrogen bromide

1968 ◽  
Vol 21 (7) ◽  
pp. 1711
Author(s):  
DA Kairaitis ◽  
VR Stimson
Keyword(s):  
Carbon Monoxide ◽  
Gas Phase ◽  
Decomposition Product ◽  
Methyl Formate ◽  
Arrhenius Equation ◽  
Hydrogen Bromide ◽  
Radical Chain ◽  
Hydrogen Halides ◽  
Chain Decomposition ◽  
First Order

Hydrogen bromide catalyses the decomposition of methyl formate into carbon monoxide and methanol at 390-460�. The radical chain decomposition product, methane, is formed in only a small amount that is further reduced by the addition of inhibitor. The reaction is homogeneous and molecular, is first order in each reactant, and follows the Arrhenius equation: k2 = 1012.50exp(-32200/RT)sec-1 ml mole-1 It is not reversed by added methanol.

Catalysis by hydrogen halides in the gas phase. XIV. Methyl trimethylacetate and hydrogen bromide and the effects of added alcohols

1968 ◽  
Vol 21 (3) ◽  
pp. 687 ◽  
Author(s):  
JTD Cross ◽  
VR Stimson
Keyword(s):  
Carbon Monoxide ◽  
Methyl Ester ◽  
Gas Phase ◽  
Hydrogen Chloride ◽  
Hydrogen Bromide ◽  
Hydrogen Halides ◽  
Kinetic Form

Hydrogen bromide and hydrogen chloride catalyse the decomposition of methyl trimethylacetate into isobutene, carbon monoxide, and methanol at 370-442� and 450-48O�, respectively. The kinetic form, which is basically 1 : 1, is severely modified by the effect of methanol either produced in the reaction or added initially. Water or alcohols react with an intermediate in the catalysed decomposition of trimethylacetic acid or its methyl ester in esterification-like reactions; some of the resultant esters subsequently decompose to olefin and acid.

Catalysis by hydrogen halides in the gas phase. XIII. Isopropanol and hydrogen iodide

1967 ◽  
Vol 20 (6) ◽  
pp. 1143 ◽  
Author(s):  
RL Failes ◽  
VR Stimson
Keyword(s):  
Gas Phase ◽  
Hydrogen Chloride ◽  
Rate Constants ◽  
Arrhenius Equation ◽  
Hydrogen Bromide ◽  
Hydrogen Iodide ◽  
Initial Reaction ◽  
Hydrogen Halides ◽  
The Individual

Hydrogen iodide catalyses the decomposition of isopropanol into propene and water at 356 to 457�, viz. �������������������������� i-C3H7OH+HI → C3H6+H2O+HI This is followed by the faster reactions �������������������������� C3H6+HI → i-C3H7I ����� ��������������������i-C3H7I+HI → C3H8+I2������������������������ i-C3H7OH+I2 → (CH3)2CO+2HI The rates of the initial reaction fit the Arrhenius equation ����������������� k2 = 1012.24 exp(-31900/RT) sec-1 ml mole-1 and it is believed to be homogeneous and molecular. It is faster than the corresponding reactions with hydrogen chloride and hydrogen bromide in the ratios 100 : 1 and 5 : 1, respectively. For the overall reaction the amounts of the products formed to 70% reaction, computed with the use of rate constants of the individual reactions, agree well with the amounts found by analysis.

Catalysis by hydrogen halides in the gas phase. XIX. 2,3-Dimethylbutan-2-ol and hydrogen bromide

1968 ◽  
Vol 21 (10) ◽  
pp. 2385 ◽  
Author(s):  
RL Johnson ◽  
VR Stimson
Keyword(s):  
Gas Phase ◽  
Arrhenius Equation ◽  
Hydrogen Bromide ◽  
Phase Decomposition ◽  
Hydrogen Halides ◽  
First Order

The gas-phase decomposition of 2,3-dimethylbutan-2-ol into 2,3-dimethylbut-1-ene, 2,3-dimethylbut-2-ene, and water, catalysed by hydrogen bromide at 303-400�, is described. The rate is first-order in each reactant and the Arrhenius equation k2 = 1011.88 exp(-26490/RT) sec-l ml mole-1 is followed. The olefins appear to be in their equilibrium proportions. The effects of substitutions in the alcohol at Cα and Cβ on the rate are discussed.

Catalysis by hydrogen halides in the gas phase. XXIII. 1,1-Dimethoxyethane and hydrogen bromide

1971 ◽  
Vol 24 (5) ◽  
pp. 961 ◽  
Author(s):  
VR Stimson
Keyword(s):  
Gas Phase ◽  
Vinyl Ether ◽  
Arrhenius Equation ◽  
Hydrogen Bromide ◽  
Phase Decomposition ◽  
Hydrogen Halides ◽  
Methyl Vinyl ◽  
First Order ◽  
Methyl Vinyl Ether

Hydrogen bromide catalyses the gas-phase decomposition of 1,1- dimethoxy-ethane at 233-322� into methyl vinyl ether and methanol. The reaction, first-order in each reactant, is believed to be homogeneous and molecular. ��� The Arrhenius equation ������ �����������k2 = 1.3x1013exp(-22160/RT) s-1 cm3 mol-1 is followed. This decomposition is much faster than the analogous reactions of alcohols and ethers. The catalyst is effective when present in only 1% proportion.

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