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Hydrocarbon Compounds
Hydrocarbon Compounds

View/Open
View/Open

Changing counterion can switch the preference for selective 1,2
Changing counterion can switch the preference for selective 1,2

... Many reactions take advantage of the coordinating ability of the functional groups on the arene to direct functionalization of adjacent positions. This is especially common for Pd-catalyzed reactions, where the directing group also helps stabilize high oxidation state intermediates. In the example b ...
14. The Direct and Enantioselective Organocatalytic -Oxidation of Aldehydes
14. The Direct and Enantioselective Organocatalytic -Oxidation of Aldehydes

Optical basicity - Archives ouvertes HAL Artois
Optical basicity - Archives ouvertes HAL Artois

UNSATURATED HYDROCARBONS
UNSATURATED HYDROCARBONS

Elucidation of Mechanisms and Selectivities of Metal
Elucidation of Mechanisms and Selectivities of Metal

Ion Exchange Resins: Catalyst Recovery and Recycle
Ion Exchange Resins: Catalyst Recovery and Recycle

... Due to the easier workup and integration in reactor equipments, the chemical industry has a strong preference for solid catalysts, which, however, usually do not provide selectivities (chemo, regio, or stereo) comparable to those observed in the homogeneous phase.17,18 There is therefore a clear nee ...
Answers - Final Exam 2013
Answers - Final Exam 2013

Section 2 Hydrocarbons Chapter 22
Section 2 Hydrocarbons Chapter 22

... amount of hydrogen are referred to as unsaturated. • Unsaturated hydrocarbons are hydrocarbons in which not all carbon atoms have four single covalent bonds. • An unsaturated hydrocarbon has one or more double bonds or triple bonds between carbon atoms. • Carbon atoms can easily form multiple bonds ...
Document
Document

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07_chapter 1

CROSS-COUPLING REACTIONS OF ORGANOBORANES: AN EASY WAY FOR C-C BONDING
CROSS-COUPLING REACTIONS OF ORGANOBORANES: AN EASY WAY FOR C-C BONDING

Reaction of niobium and tantalum neutral clusters with low pressure
Reaction of niobium and tantalum neutral clusters with low pressure

Exam 2
Exam 2

Copper-Catalyzed Hydroalkylation of Terminal Alkynes
Copper-Catalyzed Hydroalkylation of Terminal Alkynes

Copper di-imine complexes: Structures and catalytic activity
Copper di-imine complexes: Structures and catalytic activity

nucleophile (亲核试剂)
nucleophile (亲核试剂)

Separation of alcohol/ether/hydrocarbon mixtures in
Separation of alcohol/ether/hydrocarbon mixtures in

INTRODUCTION - Open Access Repository of Indian Theses
INTRODUCTION - Open Access Repository of Indian Theses

Molecular Water Oxidation Catalysts for
Molecular Water Oxidation Catalysts for

... Molecular catalysts Molecular catalysts offer the prospect of specific tailoring of the atomic structure and composition without the constraints imposed by an extended solid lattice. Such catalysts could potentially lead to more efficient water oxidation as the O–H bond cleavage and O–O bond forming r ...
Syntheses of Variations of Stereogenic-at
Syntheses of Variations of Stereogenic-at

... Mo(NAd)(CHCMe2Ph)(ORF6)(HMT) (8) as a crystalline yellow solid. 4. Testing of the novel catalysts in ROMP ROMP polymerization of 2,3-dicarbomethoxynorbornadiene (DCMNBD) has been used as a test to determine whether a given catalyst can produce a polymer with a single structure. Among the tested cata ...
Design of Nanostructured Catalysts for H2 Production
Design of Nanostructured Catalysts for H2 Production

... catalysts has a profound effect on the catalytic activity. A heterogeneous catalytic reaction begins with the adsorption of the reacting gases or liquids on the surface of the catalyst, where intramolecular bonds are broken or weakened. Next, the adsorbed species react on the surface, often in sever ...
as a PDF
as a PDF

9851a doc..9851a chapter .. Page97
9851a doc..9851a chapter .. Page97

... moisture level required, in this case by heating in vacuo at 70 °C for 24 h. TPAP catalysed oxidations with NMO as co-oxidant Investigations were initially conducted in the ionic liquid [bmim][BF4]. This ionic liquid was chosen because it is stable to air and moisture, as well as being simple and in ...
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Fischer–Tropsch process

The Fischer–Tropsch process is a collection of chemical reactions that converts a mixture of carbon monoxide and hydrogen into liquid hydrocarbons. It was first developed by Franz Fischer and Hans Tropsch at the Kaiser-Wilhelm-Institut für Kohlenforschung in Mülheim an der Ruhr, Germany, in 1925. The process, a key component of gas to liquids technology, produces a synthetic lubrication oil and synthetic fuel, typically from coal, natural gas, or biomass. The Fischer–Tropsch process has received intermittent attention as a source of low-sulfur diesel fuel and to address the supply or cost of petroleum-derived hydrocarbons. A Fischer–Tropsch-type process has also been suggested to have produced a few of the building blocks of DNA and RNA within asteroids.
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