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Sulfur oxygen

The organic chemical structural types believed to be characteristic of coals include complex polycyclic aromatic ring systems with connecting bridges and varied oxygen-, sulfur-, and nitrogen-containing functionalities. [Pg.132]

When the 2-hydroxy group of a monosaccharide reacts with (diethylamino)sulfur trifluoride (DAST), quantitative and stereoselective rearrangements are observed (K.C Nico-laou, 1986). This reaction may simultaneously introduce fluorine to C-1 and a new oxygen, sulfur, or nitrogen residue to C-2 with inversion of configuration. [Pg.272]

C. 2-Thio-4-oxoselenazolidines (and their oxygen, sulfur, and nitrogen homologs)... [Pg.274]

Alkyl hydrogen sulfates can be converted to alcohols by heating them with water This IS called hydrolysis, because a bond is cleaved by reaction with water It is the oxygen-sulfur bond that is broken when an alkyl hydrogen sulfate undergoes hydrolysis... [Pg.246]

Temp. Hydrogen sulfide Methane Nitric oxide Nitrogen Oxygen Sulfur dioxide ... [Pg.365]

It is easy to reduce anhydrous rare-earth hatides to the metal by reaction of mote electropositive metals such as calcium, lithium, sodium, potassium, and aluminum. Electrolytic reduction is an alternative in the production of the light lanthanide metals, including didymium, a Nd—Pt mixture. The rare-earth metals have a great affinity for oxygen, sulfur, nitrogen, carbon, silicon, boron, phosphoms, and hydrogen at elevated temperature and remove these elements from most other metals. [Pg.541]

Acid Oxidation. Reactions of lead with acid and alkaUes are varied. Nitric acid, the best solvent for lead, forms lead nitrate acetic acid forms soluble lead acetate in the presence of oxygen sulfuric acid forms insoluble lead sulfate. Sulfuric acid is stored in containers with chemical or acid-grade lead. Lead dissolves slowly in HCl, but in the presence of aqueous alkaUes forms soluble plumbites and plumbates. [Pg.33]

Phosgene reacts with a multitude of nitrogen, oxygen, sulfur, and carbon centers. Reaction with primary alkyl and aryl amines yield carbamoyl chlorides which are readily dehydrohalogenated to isocyanates. Secondary amines also form carbamoyl chlorides. [Pg.312]

Phosphoms shows a range of oxidation states from —3 to +5 by virtue of its electronic configuration. Elemental P is oxidized easily by nonmetals such as oxygen, sulfur, and halides to form compounds such as 2 5 2 5 reduced upon reaction with metals to generate phosphides. The... [Pg.348]

Phosphoms trichloride reacts readily with oxygen, sulfur, chlorine, and water. It serves as an intermediate in the production of phosphoms oxychloride, phosphoms sulfochloride, phosphoms pentachloride, and phosphonic (phosphorous) acids. PCl is also the raw material for the manufacture of dialkyl phosphonates,... [Pg.368]

Oxidizing elements such as oxygen, sulfur, and halides react with zinc at room temperature in the presence of moisture, but do not in its absence. At higher temperature, the reactions can be vigorous even when dry. Eor instance, a powdered mixture of zinc and sulfur explodes if warmed and zinc reacts... [Pg.398]

Type Carbon Hydrogen Oxygen Sulfur Ash Volatile... [Pg.543]

Calculation of group increments for oxygen, sulfur and nitrogen compounds has allowed the estimation of conventional ring-strain energies (CRSE) for saturated heterocycles from enthalpies of formation. For 1,3-dioxolane, CRSE is about 20 kJ mol . In 2,4-dialkyl-l,3-dioxolanes the cis form is always thermodynamically the more stable by approximately 1 kJ mol" . [Pg.32]

Under low-dose conditions, forest ecosystems act as sinks for atmospheric pollutants and in some instances as sources. As indicated in Chapter 7, the atmosphere, lithosphere, and oceans are involved in cycling carbon, nitrogen, oxygen, sulfur, and other elements through each subsystem with different time scales. Under low-dose conditions, forest and other biomass systems have been utilizing chemical compounds present in the atmosphere and releasing others to the atmosphere for thousands of years. Industrialization has increased the concentrations of NO2, SO2, and CO2 in the "clean background" atmosphere, and certain types of interactions with forest systems can be defined. [Pg.116]

High-temperature hot corrosion has been known since the 1950s. It is an extremely rapid form of oxidation that takes place at temperatures between 1500°F/816°C and 1700°F/927°C in the presence of sodium sulfate (Na2S04). Sodium sulfate is generated in the combustion process as a result of the reaction between sodium, sulfur, and oxygen. Sulfur is present as a natural contaminant in the fuel. [Pg.418]

The replacement of a substituent on an aromauc nng by a nucleophile is termed arylaUon. This chapter considers the replacement by nucleophihc oxygen, sulfur, nitrogen, and carbon of aromatic fluonne atoms, which are often activated by electron-withdrawing groups. [Pg.501]

Zinc and cadmium tarnish quickly in moist air and combine with oxygen, sulfur, phosphorus and the halogens on being heated. Mercury also reacts with these elements, except phosphorus and its reaction with oxygen was of considerable practical importance in the early work of J. Priestley and A. L. Lavoisier on oxygen (p. 601). The reaction only becomes appreciable at temperatures of about 350° C, but above about 400°C HgO decomposes back into the elements. [Pg.1205]

The concept of mesohydric tautomerism was advanced by Hunter and his associates in a series of papers which appeared between 1940 and 1950 (e.g., references 15 and 16). This concept was based on the fact that in all cases where the mobile hydrogen atom would be bonded to oxygen, sulfur, or nitrogen atoms in both possible tautomers, the individual forms had not been isolated. It was further established that many of these compounds were associated both in the liquid state and in solution, and it was concluded that the individual tautomers did not exist. The actual molecules were thought to be intermolec-ularly hydrogen-bonded, the mobile hydrogen atom being bonded equally to both of the hetero atoms. This concept has been useful and has led to clarification of the tautomerism which occurs in solids and... [Pg.316]

Solid fuels, unlike gases and liquids, are entirely characterized by their composition. For example, coal can be characterized by its carbon, hydrogen, oxygen, sulfur, and nitrogen content. The water and mineral content of coal are also important means of differentiating coals from various sources. [Pg.273]


See other pages where Sulfur oxygen is mentioned: [Pg.551]    [Pg.378]    [Pg.115]    [Pg.439]    [Pg.379]    [Pg.45]    [Pg.50]    [Pg.380]    [Pg.83]    [Pg.383]    [Pg.383]    [Pg.49]    [Pg.116]    [Pg.406]    [Pg.286]    [Pg.79]    [Pg.2]    [Pg.2]    [Pg.228]    [Pg.620]    [Pg.534]    [Pg.1]    [Pg.340]    [Pg.79]    [Pg.134]    [Pg.12]    [Pg.70]   
See also in sourсe #XX -- [ Pg.277 , Pg.278 , Pg.299 , Pg.413 , Pg.416 , Pg.531 , Pg.532 , Pg.560 , Pg.588 , Pg.600 ]




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1,4-sulfur-oxygen interactions

A 2 Elements Oxygen, Silicon, Sulfur, Chlorine, and Bromine

Addition of Carbon, Oxygen, Nitrogen, and Sulfur Nucleophiles

Atmosphere sulfur dioxide reaction with oxygen

Bidentates Sulfur-oxygen ligands

Carbon, Nitrogen, Oxygen, Phosphorus, and Sulfur

Carbon-boron-sulfur-oxygen rings

Carbon-nitrogen-oxygen-sulfur rings

Carbon-oxygen—sulfur rings

Compounds Containing Sulfur-Oxygen Bonds

Containing Carbon, Sulfur, Fluorine, and Elements other than Oxygen

Containing metal-oxygen bonds sulfur ligands

Diorgano Oxygen Sulfur (or Selenium) Tellurium Compounds

Four-membered Heterocycles containing a Single Nitrogen, Oxygen or Sulfur Atom

Functional groups sulfur-oxygen double bond

Group 16 systems sulfur-oxygen rings

Group 16 systems sulfur/selenium/tellurium-oxygen

Group Oxygen Selenium Sulfur

Group VIA Oxygen and the Sulfur Family

Halogen sulfur—oxygen bonds

Halogenation, Oxygenation and Sulfuration

Heterocycles can have many nitrogens but only one sulfur or oxygen in any ring

Heterocycles containing both oxygen and sulfur in the same ring

Hybridization of Nitrogen, Oxygen, Phosphorus, and Sulfur

Hydrogen carbon-oxygen-sulfur system

Hydrogen oxygen/nitrogen/sulfur content

Hydrogenation of Oxygen- and Sulfur-containing Aromatic Ring Systems

Iron sulfur clusters oxygenates

Lead, sulfur, oxygen system

Metal sulfur—oxygen bonds

Metal-oxygen-sulfur systems

Nitrogen sulfur—oxygen bonds

Nitrogen, sulfur and oxygen

Nitrogen, sulfur and oxygen compounds

Nitrogen—oxygen bonds sulfur halides

Nonmetal Nitrogen Oxygen Phosphorus Sulfur

Of oxygen- and sulfur-containing

Of oxygen- and sulfur-containing heterocycles

Organic Oxygen and Sulfur Radicals

Oxygen Acids of Sulfur, Selenium, and Tellurium

Oxygen Versus Sulfur Stabilization of Carbenium Ions

Oxygen acids of sulfur

Oxygen and Sulfur

Oxygen and Sulfur Derivatives

Oxygen and Sulfur Donor Ligands

Oxygen and Sulfur as Nucleophiles

Oxygen and sulfur as nucleophiles ethers, esters, thioethers, epoxides

Oxygen and sulfur atoms

Oxygen spent sulfuric acid regeneration

Oxygen sulfur burning

Oxygen sulfur burning exit gas

Oxygen sulfur halides

Oxygen sulfuric acid

Oxygen to sulfur

Oxygen with sulfur tetrafluoride

Oxygen, Silicon and Sulfur

Oxygen-sulfur bonds, reductive cleavage

Oxygen-sulfur chelates

Oxygen-sulfur rings

Oxygen—sulfur bonds

Oxygen—sulfur bonds elemental halogens

Oxygen—sulfur bonds hydrogen halides

Phosphorus—oxygen bonds sulfur halides

Photochemistry of oxygen- and sulfur-containing

Photochemistry of oxygen- and sulfur-containing heterocycles

Polymers Containing Oxygen, Nitrogen, Silicon, and Sulfur in the Backbone

Preparation of RMgX, where X is an oxygen, nitrogen or sulfur ligand

Protons on Oxygen, Nitrogen, and Sulfur Atoms

Reaction with Oxygen and Sulfur Nucleophiles

Reactions Involving Oxygen and Sulfur

Reactions with sulfur—oxygen bonds

Replacement of oxygen by sulfur groups

Replacement of sulfur by oxygen

Replacement, benzenesulfonate groups oxide oxygen atom by sulfur

Ring Systems Containing One Oxygen or Sulfur

Selenium sulfur—oxygen bonds

Silicon sulfur—oxygen bonds

Subject sulfur—oxygen bonds

Sulfur arsenic—oxygen bonds

Sulfur atoms, electronic states with oxygen

Sulfur boron-oxygen bonds

Sulfur dioxide by oxygen

Sulfur dioxide equilibrium reaction with oxygen

Sulfur dioxide reaction with oxygen

Sulfur dioxide-oxygen fuel cell

Sulfur oxygen flask combustion determination

Sulfur phosphorus—oxygen bonds

Sulfur polonium—oxygen bonds

Sulfur ratio, oxygen

Sulfur reaction with oxygen

Sulfur tellurium—oxygen bonds

Sulfur, Oxygen and Nitrogen Molar Balances

Sulfur-Nitrogen Rings Containing Exocyclic Oxygen

Sulfur-and oxygen-containing compounds

Sulfur-carbon-oxygen cycle

Sulfur-nitrogen-oxygen compounds

Sulfur-nitrogen-oxygen compounds amides

Sulfur-oxygen bond forming reactions

Sulfur-oxygen compounds

Sulfur-oxygen compounds reaction with, phosgene

Sulfur-oxygen ligands

Sulfur: oxygen oxidoreductase

Tetraorganolead Compounds Containing Oxygen and Sulfur

Thallium—oxygen bonds sulfur

Unsubstituted Triorganotin Carboxylates Derived from Oxygen and Sulfur Containing Acids

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