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Reactions hydrogen and

Catalysis by radicals will usually be due to a radical addition or displacement reaction, hydrogen and halogen being the atoms on which the displacement most often occurs. It is usually a chain reaction once the substrate is converted into a radical it carries the reaction to many molecules of substrate. Examples are polymerization and autoxidation. [Pg.248]

Cationic zirconocenes serve as useful reagents in such diverse fields as alkene polymerization, carbohydrate chemistry, asymmetric catalysis, and so on. Reagents that were originally developed for polymerization reactions (MAO, ansa-metallocenes, non-nucleophi-lic borate counterions) have now found use in organic synthesis and are being employed for carbometalation reactions, hydrogenation, and Diels—Alder catalysis. [Pg.315]

In the above reaction, hydrogen and sodium exchange places. This reaction results in the acid and base neutralizing each other. [Pg.56]

There are several lines of evidence that nucleosynthesis takes place in stars. The compositions of the outer envelopes of evolved low- and intermediate-mass stars show enhancements of the products of nuclear reactions (hydrogen and helium burning and s-process nucleosynthesis, as defined below). The ejecta of supemovae (stellar explosions) are highly enriched in short-lived radioactive nuclides that can only have been produced either just before or during the explosion. At the other extreme, low-mass stars in globular clusters, which apparently formed shortly after the universe formed, are deficient in metals (elements heavier than hydrogen and helium) because they formed before heavy elements were synthesized. [Pg.58]

Asymmetric catalysis allows chemicals to be manufactured in their enantiomer-ically pure form and reduces derivatisation and multiple purification steps that would otherwise be required. The 2001 Nobel Prize was awarded for two of the most important asymmetric reactions hydrogenations and oxidations. A variety of ligands suitable for asymmetric reductions are available commercially including BINAP, Figure 3.16. A BINAP Rh complex is used in the commercial production of 1-menthol to enantioselectively hydrogenate an alkene bond (Lancaster, 2002). Ru BINAP complexes can be used in asymmetric reductions of carbonyl groups (Noyori, 2005 Noyori and Hashiguchi, 1997). [Pg.68]

By-products from reaction Hydrogen and oxygen gases)... [Pg.112]

Volmer turned his attention to processes at - nonpo-larizable electrodes [iv], and in 1930 followed the famous publication (together with - Erdey-Gruz) on the theory of hydrogen - overpotential [v], which today forms the background of phenomenological kinetics of electrochemistry, and which resulted in the famous - Butler-Volmer equation that describes the dependence of the electrochemical rate constant on applied overpotential. His major work, Kinetics of Phase Formation , was published in 1939 [v]. See also the Volmer reaction (- hydrogen), and the Volmer biography with selected papers [vi]. [Pg.695]

Esterification/ alkylation, deNOx reaction, hydrogenation, and Zeolite molecular sieve membrane It is found that zeolite membranes, disk, and coating show high performance or potential as catalysts compared with conventional catalysts [160]... [Pg.131]

A more spectacular gaseous titration technique is used for the estimation of the concentrations of various atomic species. This involves the use of a fast flow discharge apparatus and the spectroscopic estimation of the extent of various chemiluminescent reactions. Hydrogen and nitrogen atoms may both be titrated with NO, and oxygen atoms with N02 or the reactions being... [Pg.78]

When you read the equation, the reactants in the forward reaction are on the left. In the reverse reaction, the reactants are on the right. In the forward reaction, hydrogen and nitrogen combine to form the product ammonia. In the reverse... [Pg.560]

In the first reaction, hydrogen and oxygen combine to form water vapor, whereas in the second, water vapor dissociates into hydrogen and oxygen. The equilibrium constants Ki and K2 are clearly the inverse of each other, so their product K1K2 = 1. This is true quite generally The equilibrium constant for a reverse reaction is the reciprocal of the equilibrium constant for the corresponding forward reaction. [Pg.587]

In dehydrohalogenation reactions, hydrogen and halogen are the atoms eliminated from adjacent carbons. Bases such as potassium hydroxide and sodium amide are the reagents. Both alkenes and alkynes can be synthesized by dehydrohalogenation. [Pg.89]

Thus it is the end of the hydrocarbon chain that is first attacked and the end of the aldehyde chain that is attacked in the successive reactions. Hydrogen and methane were not detected in the products. [Pg.316]

The energy that is developed by the process is normally used to heat up houses or to run engines. In a fuel cell the energy may be extracted as electrical energy directly as the transferred electrons may be extracted directly. Similarly, the simple reaction hydrogen and oxygen ... [Pg.174]

There are different types of pure substances. Elements and compounds are both pure substances. An element is a pure substance that cannot be changed into a simpler form of matter by any chemical reaction. Hydrogen and oxygen, for example, are elements. Alternatively, a compound is a substance resulting from the combination of two or more elements in a definite, reproducible way. The elements hydrogen and oxygen, as noted earlier, may combine to form the compound water, H2O. [Pg.13]

ISHIYAMA, S., UGACHI, H., ETO, M., The Performance of High Temperature Chemical Heat Pump System with Metal Hydride Reaction, Hydrogen and Clean Energy (Int. Symp., Tokyo, 1995), NEDO (1995) 337-340. [Pg.95]

The sample containing arsenite is treated with zinc/hydrochloric acid (Zn/ HCl) in a closed vessel. During this reaction, hydrogen and the volatile arsine AsHj are formed. When the hydrogen is ignited and the flame is directed to a cold surface, metallic arsenic is formed on this surface. The metallic arsenic is easily redissolved in an alkaline hydrogen peroxide solution. [Pg.30]

Esterification/alkylation, deNOx reaction, hydrogenation, and dehydrogenation studied... [Pg.207]

Light, mechanical shock, heat, and certain catalysts can be initiators of explosive reactions. Hydrogen and chlorine react explosively in the presence of light. Examples of shock-sensitive materials include acetylides, azides, organic nitrates, nitro compounds, perchlorates, and many peroxides. Acids, bases, and other substances can catalyze the explosive polymerizations. The catalytic effect of metallic contamination can lead to explosive situations. Many metal ions can catalyze the violent decomposition of hydrogen peroxide. [Pg.100]

In this reaction, hydrogen and oxygen form covalent bonds with one another. Recall from Section 10.2 that a single covalent bond is a shared electron pair. [Pg.577]


See other pages where Reactions hydrogen and is mentioned: [Pg.72]    [Pg.293]    [Pg.302]    [Pg.358]    [Pg.11]    [Pg.480]    [Pg.61]    [Pg.224]    [Pg.168]    [Pg.289]    [Pg.270]    [Pg.1281]    [Pg.2921]    [Pg.201]    [Pg.18]    [Pg.9]    [Pg.410]    [Pg.845]    [Pg.27]    [Pg.11]    [Pg.103]    [Pg.1446]    [Pg.322]    [Pg.60]    [Pg.1446]    [Pg.31]    [Pg.344]    [Pg.58]   


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Aldol Reactions in Bronsted Acid and Hydrogen-Bond Catalysis

Catalytic reactions involving CO and hydrogen formation

Catalytic reactions involving CO and hydrogenation using water

Cellobiosides, alkyl and aryl poly-0acetyl-«- , reaction with hydrogen bromide heptaacetate

Dimetallation, Hydrometallation, and Hydrogenation Reactions

Direct Hydrogen Cyanide Synthesis and Water-gas Shift Reaction

Dirhodium(ll) Carboxamidates for Asymmetric Cyclopropanation and Carbon-Hydrogen Insertion Reactions

Exchange reactions between hydrogen and deuterium

Formaldehyde, reaction with ethyl pnitrophenylacetate and hydrogen

General features of the reaction between hydrogen and oxygen

Hydrogen Abstraction and Fragmentation Reactions

Hydrogen Bonds and Proton Abstraction Reactions

Hydrogen Exchange Reaction of Arenium Ions and their Precursors

Hydrogen Oxidation and Evolution Reactions

Hydrogen Transfer in Organic and Organometallic Reactions

Hydrogen-Transfer and Dehydrogenation Reactions

Hydrogenation Reactions and Other Possibilities

Hydrogenation Reactions in Dense Gas Systems Gary Combes, Fariba Dehghani, Raffaella Mammucari, and Neil R. Foster

Hydrogenation and Hydroformylation Reactions in Alternative Solvents

Hydrogenation and Hydrosilylation Reactions

Hydrogenation and Other Reduction Reactions

Hydrogenation and Related Reactions

Hydrogenation and hydroformylation reactions

Hydrogenation, hydrogen transfer and hydrosilylation reactions assisted by boranes

Hydrogenations and Other Catalytic Reactions

Hydrogenolysis and Hydrogenation Reactions

Interference of Hydrogen Peroxide Dissociation and Substrate Oxidation Reactions

Kinetics and thermodynamics of hydrogenation reactions

Modern Alchemy Replacing Precious Metals with Iron in Catalytic Alkene and Carbonyl Hydrogenation Reactions

Palladium-Catalyzed Homogeneous Hydrogenation with Dihydrogen and Related Hydrogen Transfer Reactions

Photo-Induced Hydrogen Abstraction and Addition Reactions of Aromatic Compounds

Preparation of Heterogeneous Catalysts for Chemo- and Enantioselective Hydrogenation Reactions

Quinones in Hydrogen Peroxide Synthesis and Catalytic Aerobic Oxidation Reactions

Reaction Intermediates and the Mechanism of Hydrogen Oxidation

Reaction Involving Hydrogen and Group Translocations

Reaction between Molecular Hydrogen and Chlorine

Reaction between Molecular Hydrogen and Iodine

Reaction of Halogens and Hydrogen Halacids

Reaction of Hydrogen and Oxygen

Reaction of acyl halides with hydrogen sulfide and its derivatives

Reaction with Free Radicals Hydrogen Atom Abstraction and One- or Three-Electron Bonding

Reaction with Oxygen and Hydrogen

Reaction with hydrogen sulfide and its derivatives

Reactions involving Oxygen and Hydrogen Peroxide

Reactions of Halogens and Hydrogen Halides

Reactions of Oxygen and Hydrogen Peroxide

Reactions with Atomic Hydrogen and Nitrogen

Reactions with Water and Hydrogen Peroxide. Alkaline Hydrolysis

Reactions with direct transfer of hydrogen between nicotinamide coenzyme and substrate

Reactions with oxygen and hydrogen peroxide

Rh and Ru Nanoparticles as Catalysts in Hydrogenation Reactions

Sulfur in Hydrogenation, Isomerization, and Related Reactions

The Phenomena of Interference in Chemical and Biochemical Redox Reactions with Hydrogen Peroxide

The Reaction between Hydrogen Peroxide and Cupric Ions

The Reaction between Hydrogen Peroxide and Ferric Ions

Third Example Proton Transfer and Hydrogen Abstraction Reactions

Transition Metal Catalyzed Hydrogenations, Isomerizations, and Other Reactions

WGS Reaction and Water Electrolysis for Hydrogen Production

Water-Gas Shift Reaction for Hydrogen Production and Other Applications

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