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Addition hydrogenation

It is a typically aromatic compound and gives addition and substitution reactions more readily than benzene. Can be reduced to a series of compounds containing 2-10 additional hydrogen atoms (e.g. tetralin, decalin), which are liquids of value as solvents. Exhaustive chlorination gives rise to wax-like compounds. It gives rise to two series of monosubstitution products depending upon... [Pg.269]

Steam reforming is, along with catalytic reforming, a process that can produce the additional hydrogen needed for upgrading and converting the heavy fractions of crude oil. [Pg.391]

Step 4 The second hydrogen atom is transferred forming the alkane The sites on the catalyst surface at which the reaction occurred are free to accept additional hydrogen and alkene molecules... [Pg.232]

In the presence of catalysts, the CO reacts with steam through the shift reaction to produce additional hydrogen and CO2 as represented by... [Pg.174]

Immobile hydrocarbon sources requite refining processes involving hydrogenation. Additional hydrogen is also requited to eliminate sources of sulfur and nitrogen oxides that would be emitted to the environment. Resources can be classified as mostiy consumed, proven but stiU in the ground, and yet to be discovered. A reasonable estimate for the proven reserves for cmde oil is estimated at 140 x 10 t (1.0 x 10 bbl) (4). In 1950 the United States proven reserves were 32% of the world s reserve. In 1975 this percentage had decreased to 5%, and by 1993 it was down to 2.5%. Since 1950 the dominance of... [Pg.364]

Reactions of Synthesis Gas. The main hydrogen manufacturing processes produce synthesis gas, a mixture of H2 and CO. Synthesis gas can have a variety of H2-to-CO ratios, and the water gas shift reaction is used to reduce the CO level and produce additional hydrogen, or to adjust the H2 to-CO ratio to one more beneficial to subsequent processing (69) ... [Pg.415]

Synthetic jet fuel derived from coal is even more difficult and expensive, since the best of the conversion processes produces a fuel very high in aromatics. With hydrogenation, overall thermal efficiency is only 50%. Without additional hydrogenation, the gas turbine fuels would contain 60—70% aromatics. [Pg.417]

Caution Because tellurium compounds have toxic effects similar to those of arsenic compounds care should be taken not to bring tellurium tetrachloride and its reaction products into contact with the skin. Avoid breathing fumes and dust of tellurium compounds. In addition, hydrogen chloride is evolved in Step A, and pyrophoric Raney nickel is used in Step B. Therefore all manipulations described in this procedure must be carried out in an efficient fume hood. [Pg.18]

The reaction produces additional hydrogen for ammonia synthesis. The shift reactor effluent is cooled and tlie condensed water is separated. The gas is purified by removing carbon dioxide from the synthesis gas by absorption with hot carbonate, Selexol, or methyl ethyl amine (MEA). After purification, the remaining traces of carbon monoxide and carbon dioxide are removed in the methanation reactions. [Pg.1126]

Ethylene is another molecule that is similar to formaldehyde. The two compounds are isoelectronic. In the case of ethylene, the oxygen in formaldehyde is replaced by a carbon with two additional hydrogens attached to it. [Pg.27]

Additionally, hydrogen atoms diffuse through metals and coalesce to form hydrogen molecules at certain preferred locations such as inclusions. [Pg.895]

B. Characteristic Fragment Ions The most characteristic cleavage is the loss of carbons 15,16, and 17, together with the side chain and one additional hydrogen. It is possible to determine the elemental composition of the side chains of steroids by the difference in the mass between the molecular ion and an intense ion more than 15... [Pg.119]

The relative amounts of double bond addition, hydrogen abstraction and 13-scission observed are dependent on the reactivity and concentration of the particular monomer(s) employed and the reaction conditions. Higher reaction temperatures are reported to favor abstraction over addition in the reaction of t-butoxy radicals with AMS413 and cyclopentadiene 417 However, the opposite trend is seen with isobutylene.2 1 24... [Pg.123]

FIGURE 9.10 These graphs show the changes in composition that can be expected when additional hydrogen and then ammonia are added to an equilibrium mixture of nitrogen, hydrogen, and ammonia. Note that the addition of hydrogen results in the formation of ammonia, whereas the addition of ammonia results in the decomposition of some of the added ammonia as reactants are formed. In each case, the mixture settles into a composition in accord with the equilibrium constant of the reaction. [Pg.498]

In addition, hydrogen bonding was still observed at 3,583 cm (Fig.l A). IR peaks in VC.O region (Fig.l B) shifted to lower frequency after adsorption due to precursor-support interaction and differed from that of cluster solution implying that precursor was not intact after adsorption on support but still in the form of metal carbonyl species. [Pg.211]

The steam reforming of natural gas process is the most economic near-term process among the conventional processes. On the other hand, the steam reforming natural gas process consists of reacting methane with steam to produce CO and H2. The CO is further reacted or shifted with steam to form additional hydrogen and CO2. The CO2 is then removed from the gas mixture to produce a clean stream of hydrogen. Normally the CO2 is vented into the atmosphere. For decarbonization, the CO2 must be sequestered[l,2]. The alternative method for hydrogen production with sequestration of carbon is the thermal decomposition of methane. [Pg.421]


See other pages where Addition hydrogenation is mentioned: [Pg.12]    [Pg.65]    [Pg.165]    [Pg.88]    [Pg.89]    [Pg.329]    [Pg.456]    [Pg.278]    [Pg.481]    [Pg.493]    [Pg.506]    [Pg.341]    [Pg.342]    [Pg.201]    [Pg.224]    [Pg.2371]    [Pg.254]    [Pg.259]    [Pg.49]    [Pg.394]    [Pg.273]    [Pg.293]    [Pg.173]    [Pg.251]    [Pg.613]    [Pg.427]    [Pg.349]    [Pg.92]    [Pg.101]    [Pg.382]    [Pg.38]    [Pg.78]    [Pg.92]    [Pg.204]   
See also in sourсe #XX -- [ Pg.11 ]

See also in sourсe #XX -- [ Pg.11 ]




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1,2-Addition proton-type hydrogen transfer

1,3-Butadiene, 1,2-addition reactions heat of hydrogenation

1.3- Butadiene hydrogen bromide addition

1.3- Butadiene hydrogen chloride addition

1.3- dienes addition of hydrogen halides

2.3- Dimethyl-2-butene hydrogen chloride addition

A Addition of hydrogen fluoride

Addition of Hydrogen Bromide to 1-Hexene

Addition of Hydrogen Chloride

Addition of Hydrogen Chloride to 1,3 Cyclopentadiene

Addition of Hydrogen Cyanide

Addition of Hydrogen Cyanide Cyanohydrins

Addition of Hydrogen Cyanide to Give Cyanohydrins

Addition of Hydrogen Cyanide to Osones Followed by Hydrolysis

Addition of Hydrogen Hahdes

Addition of Hydrogen Halides to Alkenes

Addition of Hydrogen Halides to Alkynes

Addition of Hydrogen Halides to Conjugated Dienes

Addition of Hydrogen Halides to Nitriles and Isonitriles

Addition of Hydrogen Halides to the Pyrrole Ring

Addition of a Hydrogen Halide to an Alkene

Addition of active hydrogen

Addition of hydrogen

Addition of hydrogen (reduction)

Addition of hydrogen atoms to alkenes

Addition of hydrogen bromide to ethyl acrylate

Addition of hydrogen cyanide derivatives

Addition of hydrogen cyanide to an aldehyde. Mandelic acid from benzaldehyde

Addition of hydrogen fluonde

Addition of hydrogen fluonde to alkenes

Addition of hydrogen fluoride

Addition of hydrogen fluoride to double

Addition of hydrogen fluoride to double bonds

Addition of hydrogen halide to simple unsaturated hydrocarbons

Addition of hydrogen halide to unsaturated alcohols, ethers, carbonyl compounds, and nitriles

Addition of hydrogen halides

Addition of hydrogen halides (HX)

Addition of hydrogen halides or halogens to alkenes

Addition of hydrogen peroxide

Addition of hydrogen sulfide and its derivatives

Addition of hydrogen to alkenes and alkynes catalytic hydrogenation

Addition polymers hydrogen halides

Addition processes, hydrogen

Addition reactions catalytic hydrogenation

Addition reactions hydrogen

Addition reactions hydrogen halides

Addition reactions hydrogenation

Addition reactions, of hydrogen

Addition reactions, of hydrogen halides

Additional States of Hydrogen

Additive compounds, heterogeneous hydrogenation

Additives in slowly reacting mixtures of hydrogen and oxygen

Additives, hydrogenated

Additives, hydrogenated

Alkenes addition of hydrogen

Alkenes addition of hydrogen halides

Alkenes addition reactions with hydrogen halides

Alkenes hydrogen bromide addition

Alkenes radical addition of hydrogen bromid

Alkenes, addition reactions Hydrogenation

Alkynes addition of hydrogen halides

Alkynes hydrogen halide addition

Alkynes, addition reactions hydrogenation

Anti addition of hydrogen

Anti-Markovnikov addition of hydrogen

Anti-Markovnikov addition of hydrogen bromide

Antimony fluoride catalysts addition of hydrogen

Barium chloride, catalysts addition of hydrogen

Butadiene hydrogen cyanide addition

By addition of hydrogen

Cadmium nitrate, catalysts addition of hydrogen

Carbocation Rearrangements in Hydrogen Halide Addition to Alkenes

Carbocations addition of hydrogen halides

Carbocations addition of hydrogen halides to conjugated

Carbon-hydrogen bonds oxidative addition

Carbonyl addition-elimination-hydrogenation

Carbonyl addition-elimination-hydrogenation reagent

Catalyst for additions of hydrogen

Cis-addition of hydrogen

Combination of Both Hydrogen Addition and Carbon Rejection Technologies

Conjugate addition hydrogen chloride

Conjugate addition of hydrogen cyanide

Conjugate addition reactions hydrogen bonding

Cycloalkenes addition of hydrogen halides

Cyclohexenes stereochemistry of hydrogen halide addition

Dihydro Addition - Cycloalkene Hydrogenation

Double bonds s. a. Addition Hydrogenation, Migration

Electrophilic Addition of Hydrogen Bromide to 2-Methylpropene

Electrophilic Addition of a Hydrogen Halide to an Alkene

Electrophilic addition hydrogen halides

Electrophilic addition hydrogenation

Electrophilic addition of hydrogen halides to alkenes

Electrophilic addition reactions, alkynes hydrogen halides

Elimination/addition reactions hydrogenation reaction

Enantioselective Conjugate Addition Reactions via Hydrogen-bonding Activation

For additions of hydrogen

For additions of hydrogen fluonde to alkenes

Free radical addition of hydrogen bromide to alkene

Free-Radical Addition of Hydrogen Bromide to 1-Butene

Free-radical addition of hydrogen bromide

Hahdes hydrogen, additions

Hydrogen Addition Technologies

Hydrogen addition

Hydrogen addition reactions with

Hydrogen addition reactions with behavior

Hydrogen addition reactions with cluster size-dependent

Hydrogen addition reactions with clusters

Hydrogen addition reactions with constants

Hydrogen addition, stepwise 11/11 transfer

Hydrogen addition, thymine hydroperoxides

Hydrogen anti addition

Hydrogen atoms, addition

Hydrogen bonding in addition

Hydrogen bonding, conjugate addition

Hydrogen bonding, conjugate addition determination

Hydrogen bromide electrophilic addition

Hydrogen bromide free radical addition

Hydrogen bromide free-radical addition, alkenes

Hydrogen bromide, addition

Hydrogen bromide, addition mechanism

Hydrogen bromide, addition to alkenes

Hydrogen bromide, anti-Markovnikov addition

Hydrogen bromide, anti-Markovnikov addition alkenes

Hydrogen chloride addition

Hydrogen cyanide addition

Hydrogen cyanide addition reactions

Hydrogen cyanide conjugate addition

Hydrogen cyanide conjugate vs. direct addition

Hydrogen cyanide, addition to ethyl

Hydrogen cyanide, addition to ethyl crotonate

Hydrogen fluoride addition to alkynes

Hydrogen halide addition Markovnikov’s rule

Hydrogen halides addition

Hydrogen halides addition to alkenes

Hydrogen halides addition to alkynes

Hydrogen halides electrophilic addition, alkynes

Hydrogen halides, addition fluoroalkenes

Hydrogen oxidative addition

Hydrogen oxidative addition, </8 species

Hydrogen peroxide, addition

Hydrogen peroxide, addition platinum complexes

Hydrogen photochemical addition

Hydrogen scavenger, addition

Hydrogen sulfide, addition

Hydrogen sulfide, addition alkenes

Hydrogen sulfide, addition with carbonyl compounds

Hydrogen, polymerisation additions

Hydrogen-bonding additives

Hydrogen-bonding additives in conjugated dienes

Hydrogen-bonding additives in conjugated trienes

Hydrogen-bonding additives in prismanes

Hydrogen-bonding additives trienes

Hydrogenation Addition of hydrogen

Hydrogenation The addition of hydrogen

Hydrogenation anti addition

Hydrogenation apparent anti addition

Hydrogenation heat addition

Hydrogenation hydrogen halides, additions

Hydrogenation or Other Addition to the Double Bond of Unsaturated 1,3-Oxazines

Hydrogenation syn addition

Hydrogenative addition

Hydrogenative addition

In additions hydrogen fluonde to double

In additions of hydrogen

In additions of hydrogen fluondes

Inorganic additives hydrogen sulfates

Ionic addition of hydrogen

Isocyanates, addition catalytic hydrogenation

Mechanism hydrogen halide addition

Mercuric nitrate, catalysts addition of hydrogen

Mercuric oxide catalyst addition of hydrogen

Nitriles addition of hydrogen fluonde

Nitrosyl hydrogen sulfate addition to alkenes

Norbomene addition of hydrogen halides

Nucleophilic addition hydrogen cyanide

Nucleophilic addition of hydrogen fluoride

Nucleophilic addition reactions hydrogen nucleophiles

Nucleophilic addition reactions with hydrogen nucleophiles

Olefin hydrogenation Michael addition

Oxidative addition heterogeneous hydrogenation

Oxidative addition hydrogen molecule

Oxidative addition of hydrogen

Oxidative addition of molecular hydrogen to low valent

Pairwise additive interactions, hydrogen

Photo-Induced Hydrogen Abstraction and Addition Reactions of Aromatic Compounds

Polar addition hydrogen halides

Potential energy addition of hydrogen bromide

Primary hydrogen addition

Propiolic acid addition of hydrogen halides

Radical addition hydrogen bromide

Radical mechanism, addition hydrogen

Radical-chain addition, of hydrogen bromide

Reaction L.—(a) Addition of Hydrogen Cyanide to Aldehydes or Ketones

Rearrangements in hydrogen halide addition to alkenes

Reduction by addition of hydrogen

Regioselectivity addition of hydrogen halides

Regioselectivity of Hydrogen Halide Addition Markovnikovs Rule

Regiospecificity of Hydrogen Halide Addition

Reversible Hydrogen Additions to Reduced Porphyrins

Self-Ignition of Hydrogenous Mixtures with Hydrocarbon Fuel Additives

Stereoselectivity addition of hydrogen halides to alkenes

Styrene addition of hydrogen bromide

Syn and Apparent Anti Addition of Hydrogen

Syn-addition of hydrogen

The ADDITION OF ACIDS TO OLEFINS THROUGH ELECTROPHILIC HYDROGEN

The Addition of Hydrogen Cyanide Cyanohydrins

The Addition of Hydrogen to an Alkene

The Addition of Hydrogen to an Alkyne

Thermodynamic control addition of hydrogen bromide

Thioureas, as hydrogen-bonding additives

Topside addition of hydrogen

Trans-addition during hydrogenation

Trans-addition of hydrogen

Ureas as hydrogen-bonding additives

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