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To oxygen

In practice, for motors, turbines or furnaces, the conditions of combustion are frequently far from those corresponding to stoichiometry and are characterized either by an excess or by an insufficiency of fuel with respect to oxygen. The composition of the fuel-air mixture is expressed by the equivalence ratio, (p, defined by the relation / 5 r)... [Pg.179]

The development of catalytic converters for combustion of unburned hydrocarbons prohibits a return to lead compounds and henceforth refiners are turning to oxygenated compounds that must be used as a gasoline component therefore, in amounts much greater than those of lead compounds. [Pg.346]

When investigating time parameters it was shown, that a storage time in Xe of spectral purity was 10 mcs, while a restoring time was 10 ms with subsequent decrease in the case of addition of small amounts of air (less than 1%). As basic processes influencing time parameters, both dissociative recombination and three-particle adhesion of electrons to oxygen molecules have been considered. [Pg.539]

An example of the fomiation of a new reconstmction is given by certain fee (110) metal surfaces. The clean surfaces have (1x1) synunetry, but become (2x1) upon adsorption of oxygen [16, 38]. The (2x1) synuiietry is not just due to oxygen being adsorbed into a (2 x 1) surface unit cell, but also because the substrate atoms rearrange themselves... [Pg.299]

The effects of TIP also appear in figure B 1,11.3 and figure B 1.11.4. In the NMR spectrum, all the resonances of the sp carbons lie above 100 ppm (a usefiil general rule of thumb) because A is smaller for multiple bonds. The highest shifts are for the carbonyl C at 169 ppm and the ring C attached to oxygen at 155... [Pg.1447]

It decomposes exothermically to oxygen, a reaction which can be explosive. Even dilute ozone decomposes slowly at room temperature the decomposition is catalysed by various substances (for example manganese(IV) oxide and soda-lime) and occurs more rapidly on heating. [Pg.264]

Hydrogen peroxide has both oxidising properties (when it is converted to water) and reducing properties (when it is converted to oxygen) the half-reactions are (acid solution) ... [Pg.280]

Once the atoms arc defined, the bonds between them arc specified in a bond block. Each line of this block specifies which two atoms are bonded, the multiplicity of the bond (the bond type entry) and the stereo configuration of the bond (there arc also three additional fields that arc unused in Molfiles and usually set to 0). The indices of the atoms reflect the order of their appearance in the atom block. In the example analyzed, V relates to the first carbon atom (see also Figure 2-24). "2" to the second one, 3" to oxygen atom, etc. Then the two first lines of the bond block of the analyzed file (Figure 2-29) describe the single bond between the two carbon atoms C1-C2 and the double bond C2=0-5, respectively. [Pg.50]

A wider variety of reaction types involving reactions at bonds to oxygen atom bearing functional groups was investigated by the same kind of methodology [30]. Reaction classification is an essential step in knowledge extraction from reaction databases. This topic is discussed in Section 10.3.1 of this book. [Pg.196]

As special cases lo these ratlii, belter values are used for the elements boron to oxygen (br particular bybrifli/alion stales. [Pg.210]

When hydrogen is burned up in the nuclear furnace of a star, helium burning takes over, forming carbon, which in turn leads to oxygen, etc. Subsequent emission processes releasing a-particles, equilibrium processes, neutron absorption, proton capture, etc. lead to heavier elements. [Pg.35]

In their reactions with suitable nucleophiles, such as tt-aromatics or heteroatom donor nucleophiles, the readily polarizable linear acylium ions shift a Tt-electron pair to oxygen, bending the ions and developing an empty p-orbital at the carbocationic center. This enables the reaction with aromatics. The acetylation of benzene can be depicted as... [Pg.193]

Note 1. The product is very sensitive to oxygen. All operations during the work--up must therefore be carried out under nitrogen. [Pg.43]

Note 2. In view of the sensitivity of cumulenic ethers to oxygen the work up was carried out under nitrogen with water that had been saturated with ni trogen. [Pg.46]

Acetoxybenzene is prepared by the reaction of benzene with Pd(OAc)2[325,342-345], This reaction is regarded as a potentially useful method for phenol production from benzene, if carried out with only a catalytic amount of Pd(OAc)2. Extensive studies have been carried out on this reaction in order to achieve a high catalytic turnover. In addition to oxygen and Cu(II) salts, other oxidants, such as HNOi, nitrate[346,347], potassium peroxodisulfate[348], and heteropoly acids[349,3S0], are used. HNO is said to... [Pg.76]

In many acids the acidic proton is bonded to oxygen Such compounds can be con sidered as derivatives of water Among organic compounds the ones most closely related to water are alcohols Most alcohols are somewhat weaker acids than water methanol IS slightly stronger... [Pg.40]

Step 3 Carbon migrates from boron to oxygen displacing hydroxide ion Carbon migrates with the pair of electrons m the carbon-boron bond these become the electrons m the carbon-oxygen bond... [Pg.255]

Representation of transition state for migration of carbon from boron to oxygen... [Pg.255]

Ethers are described as symmetrical or unsymmetrical depending on whether the two groups bonded to oxygen are the same or different Unsymmetrical ethers are also called... [Pg.665]

The mechanism of enolization involves two separate proton transfer steps rather than a one step process m which a proton jumps from carbon to oxygen It is relatively slow m neutral media The rate of enolization is catalyzed by acids as shown by the mechanism m Figure 18 1 In aqueous acid a hydronium ion transfers a proton to the carbonyl oxygen m step 1 and a water molecule acts as a Brpnsted base to remove a proton from the a car bon atom m step 2 The second step is slower than the first The first step involves proton transfer between oxygens and the second is a proton transfer from carbon to oxygen... [Pg.759]

NMR Similarly carbons that are bonded to nitrogen are more shielded than those bonded to oxygen as revealed by comparing the chemical shifts of methylamme and methanol... [Pg.953]

Although a hydroxyl group strongly activates an aromatic ring toward electrophilic attack an oxyanion substituent is an even more powerful activator Electron delocaliza tion m phenoxide anion leads to increased electron density at the positions ortho and para to oxygen... [Pg.1007]

The ready reversibility of this reaction is essential to the role that qumones play in cellular respiration the process by which an organism uses molecular oxygen to convert Its food to carbon dioxide water and energy Electrons are not transferred directly from the substrate molecule to oxygen but instead are transferred by way of an electron trans port chain involving a succession of oxidation-reduction reactions A key component of this electron transport chain is the substance known as ubiquinone or coenzyme Q... [Pg.1013]

FIGURE 27 19 Proposed mechanism of hydrolysis of a peptide catalyzed by carboxypeptidase A The peptide is bound at the active site by an ionic bond between its C terminal ammo acid and the positively charged side chain of arginine 145 Coordination of Zn to oxygen makes the carbon of the carbonyl group more positive and increases the rate of nucleophilic attack by water... [Pg.1147]

Because 2 chloroethanol has a proton bonded to oxygen it is not an appropnate substrate for con version to a stable Gngnard reagent... [Pg.1234]

Rotation about the carbon-nitrogen bond is slow in amides The methyl groups of NJ dimethylformamide are nonequivalent because one is cis to oxygen the other cis to hydrogen... [Pg.1236]

Protic solvent (Section 8 12) A solvent that has easily ex changeable protons especially protons bonded to oxygen as in hydroxyl groups... [Pg.1292]


See other pages where To oxygen is mentioned: [Pg.211]    [Pg.405]    [Pg.176]    [Pg.178]    [Pg.259]    [Pg.401]    [Pg.645]    [Pg.998]    [Pg.219]    [Pg.1]    [Pg.14]    [Pg.18]    [Pg.21]    [Pg.147]    [Pg.254]    [Pg.666]    [Pg.708]    [Pg.737]    [Pg.737]    [Pg.842]    [Pg.847]    [Pg.1012]    [Pg.1077]    [Pg.1268]   
See also in sourсe #XX -- [ Pg.152 ]




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Acetyl hypofluonte oxygen to double bond

Addition of Radicals to Molecular Oxygen

Addition of oxygen atoms to double and triple bonds

Addition of oxygen to ethylenic bonds

Addition to Oxygen-containing Multiple Bonds

Addition to carbon-oxygen double

Addition to carbon-oxygene double bonds

Addition to carbon/oxygen double bonds

Addition to nitrogen-oxygen double bonds

Additions of Achiral and Racemic Oxygenated Allylic Stannanes to Aldehydes

Alpha to Oxygenated Carbon

Binding of oxygen to myoglobin and hemoglobin

Bonds to Oxygen

Boron-to-oxygen migration

Carbon Bonded to Nitrogen or Oxygen

Cascade Reactions Initiated by Addition of O-Centered Radicals to Alkynes (Self-Terminating Radical Oxygenations)

Copper to Oxygen Bond Distances—Ionic Radii

Copper(II) catalyzed oxidation of primary alcohols to aldehydes with atmospheric oxygen

Correction to 7% oxygen

Corrosion due to oxygen

Coupling of Oxygen and Nitrate to other Redox Pathways

Currents due to oxygen

Effect of Oxygen-to-Vacuum Residue Ratio

Effects of Exposure to Hydrogen Peroxide Bubbled Air, Oxygen and Nitrogen

Electron attachment to oxygen

Electron coupling to oxygen vibrations

Eliminations to Form Carbon-Oxygen Double Bonds Oxidation Reactions

Energy to molecular oxygen

Generation of a Carbanion y to the Carbon-Oxygen Bond

Heterogeneous Processes in the Partial Oxidation of Methane to Oxygenates

How to Light a Gas-Oxygen Torch

Hydrocarbon gases to oxygenates

Hydrogen attached to oxygen

Langmuir-Hinshelwood approach to oxygen

Langmuir-Hinshelwood approach to oxygen quenching

Lithiation a to oxygen

Manganese-catalysed oxidation of water to oxygen

Migration of silicon, from carbon to oxygen

Naphthalenes addition to singlet oxygen

Natural gas to oxygenates

Negative conjugation - donation from oxygen lone pairs to breaking bonds

Nucleophilic Addition to the Carbon-Oxygen Double Bond

Oxygen Balance to CO . See

Oxygen Balance to CO and

Oxygen Bonded to Activated Tetrahedral Carbon Atoms

Oxygen Bonded to Trigonal Carbon Atoms

Oxygen added to acid plant gas

Oxygen addition to free radicals

Oxygen atom transfer to olefins

Oxygen binding of, to heme proteins

Oxygen binding to hemoglobin

Oxygen binding to myoglobin

Oxygen isotope zoning in subvolcanic, intrusion-centered submarine hydrothermal systems as a guide to VMS exploration

Oxygen migration to electron-deficient

Oxygen reduction to superoxide

Oxygen to carbon ratio

Oxygen to hemocyanin

Oxygen to sulfur

Oxygen to water

Oxygen transport to tissue

Oxygen transport to tissue and the Krogh-Erlang model

Oxygen-to-Carbon migration

Oxygen-to-fuel ratio

Oxygen-to-hydrocarbon ratio

Oxygen-to-metal ratio

Ozone Conversion to Oxygen in Presence of Chlorine

Permeability to oxygen

Polarization Curves for Small to Medium Oxygen Transport Loss

Proton bonded to oxygen and nitrogen

Protons Attached to Oxygen and Nitrogen

Rearrangement to Electron-Deficient Nitrogen and Oxygen

Rearrangements to Electron-Deficient Nitrogen and Oxygen Centers

Relations to Oxygen

Resistance to oxygen

Singlet oxygen addition to cyclohexadiene

Stability to oxygen

Steam-to-oxygen ratio

The Link to Oxygen

The Oxygen of an Ether Croup Is Bonded to Two Carbon Atoms

The Relation of Mononuclear Surface Oxygen Species to Electron Spectroscopic and Catalysis Studies

The aldehyde region unsaturated carbon bonded to oxygen

Transition metal clusters oxygen bonding to aluminum bromide

Use of Fluorocarbons to Carry Oxygen

Vitamin susceptibility to light, oxygen, heat and trace

Water oxidation to oxygen

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