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Carbon and compounds

A major difference between alcohols and thiols concerns their oxidation We have seen earlier m this chapter that oxidation of alcohols gives compounds having carbonyl groups Analogous oxidation of thiols to compounds with C=S functions does not occur Only sulfur is oxidized not carbon and compounds containing sulfur m various oxida tion states are possible These include a series of acids classified as sulfemc sulfimc and sulfonic according to the number of oxygens attached to sulfur... [Pg.650]

The chemical name of codeine—methylmorphine—is rather revealing, especially for those who know organic chemistry (the study of carbon and compounds containing carbon, which are referred to as organic compounds). As with mor-... [Pg.27]

Chlorine and bromine react with methane and form products in which a part or all the hydrogen is replaced by halogen. Mixtures of chlorine and methane explode when exposed to direct sunlight. Hydrochloric acid, carbon, and compounds... [Pg.28]

Note that not all carbon compounds are classified as organic compounds. The oxides of carbon and compounds containing carbonate and hydrogencarbonate ions are classed as inorganic compounds. [Pg.199]

Molecules in this category contain atoms other that carbon and hydrogen. The distinction is made between organic and organometallic compounds. [Pg.8]

The element before carbon in Period 2, boron, has one electron less than carbon, and forms many covalent compounds of type BX3 where X is a monovalent atom or group. In these, the boron uses three sp hybrid orbitals to form three trigonal planar bonds, like carbon in ethene, but the unhybridised 2p orbital is vacant, i.e. it contains no electrons. In the nitrogen atom (one more electron than carbon) one orbital must contain two electrons—the lone pair hence sp hybridisation will give four tetrahedral orbitals, one containing this lone pair. Oxygen similarly hybridised will have two orbitals occupied by lone pairs, and fluorine, three. Hence the hydrides of the elements from carbon to fluorine have the structures... [Pg.57]

The concept of oxidation states is best applied only to germanium, tin and lead, for the chemistry of carbon and silicon is almost wholly defined in terms of covalency with the carbon and silicon atoms sharing all their four outer quantum level electrons. These are often tetrahedrally arranged around the central atom. There are compounds of carbon in which the valency appears to be less than... [Pg.162]

This reaction can be reversed by heat and the potassium carbonate and carbon dioxide recovered. (Other compounds which absorb carbon dioxide and evolve it again at a lower temperature are also in common usage" ). [Pg.181]

Fusion of a manganese compound with sodium carbonate and potassium nitrate (on porcelain) gives a green manganate(VI) (p.. 86)... [Pg.390]

The elements of an organic compound are listed in empirical formulas according to the Hill system [8] and the stoichiometry is indicated by index numbers. Hill positioned the carbon and the hydrogen atoms in the first and the second places, with heteroatoms following them in alphabetical order, e.g., C9H11NO2. However, it was recognized that different compounds could have the same empirical formula (see Section 2.8.2, on isomerism). Therefore, fine subdivisions of the empirical... [Pg.20]

Divide the saturated solution of n-butyl alcohol in water into three approximately equal parts. Treat these respectively with about 2-5 g. of sodium chloride, potassium carbonate and sodium hydroxide, and shake each until the soli have dissolved. Observe the effect of these compounds upon the solubility of n-butanol in water. These results illustrate the phenomenon of salting out of organic compounds, t.e., the decrease of solubility of organic compounds in water when the solution is saturated with an inorganic compound. The alcohol layer which separates is actually a saturated solution of water in n-butyl alcohol. [Pg.260]

N-Nitrosodiethylamine. Add 36-5 g. (51-5 ml.) of diethylamine slowly to the calculated quantity of carefully standardised 5A-hydra chloric acid cooled in ice (1). Introduce the solution of the hydi ochloride into a solution of 39 g. of sodium nitrite (assumed to be of 90 per cent, purity) in 45 ml. of water contained in a 250 ml. distilling flask. Distil the mixture rapidly to dryness. Separate the yellow upper layer of the nitrosamine from the distillate saturate the aqueous layer with soUd potassium carbonate and remove the nitroso compound which separates and add it to the main product. Dry over anhydrous potassium carbonate and distil. Collect the diethylnitrosamine at 172-173-5°, The yield is 41 g. [Pg.426]

If it is desired to test directly for the presence of carbon and hydrogen in a compound, mix 01 g. of the substance with 1-2 g. of ignited, fine... [Pg.1038]

This reference work differs from Beilstein in that it is baaed upon structural formulae and compounds are grouped according to the carbon skeleton rather than the functional group the latter system has the advantage that closely related compounds are grouped together. The volumes are not published in numerical order but rather on the basis of fields of current interest. They are a valuable supplement to Beilstein. The volumes which have been published to date (1955) are ... [Pg.1129]

White phosphorus may be made by several methods. By one process, tri-calcium phosphate, the essential ingredient of phosphate rock, is heated in the presence of carbon and silica in an electric furnace or fuel-fired furnace. Elementary phosphorus is liberated as vapor and may be collected under phosphoric acid, an important compound in making super-phosphate fertilizers. [Pg.37]


See other pages where Carbon and compounds is mentioned: [Pg.650]    [Pg.111]    [Pg.147]    [Pg.490]    [Pg.605]    [Pg.490]    [Pg.605]    [Pg.200]    [Pg.490]    [Pg.490]    [Pg.650]    [Pg.111]    [Pg.147]    [Pg.490]    [Pg.605]    [Pg.490]    [Pg.605]    [Pg.200]    [Pg.490]    [Pg.490]    [Pg.80]    [Pg.83]    [Pg.98]    [Pg.167]    [Pg.208]    [Pg.241]    [Pg.89]    [Pg.1063]    [Pg.162]    [Pg.205]    [Pg.411]    [Pg.176]    [Pg.519]    [Pg.326]    [Pg.467]    [Pg.588]    [Pg.695]    [Pg.1044]    [Pg.1144]   
See also in sourсe #XX -- [ Pg.466 ]

See also in sourсe #XX -- [ Pg.63 , Pg.219 ]




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Adsorption of organic compounds onto activated carbon applications in water and air treatments

Biotransformations in the Preparation of Compounds Labeled with Carbon and Hydrogen Isotopes

Carbon Allotropes and Compounds

Carbon and some of its compounds

Carbon compounds and complexes

Centrally chiral compounds of carbon and silicon

Chemistry of Carbon and Its Compounds

Compounds of Carbon and Hydrogen - The Hydrocarbons

Compounds of Metals with Boron, Carbon, and Nitrogen

Cyanides and Other Carbon-Nitrogen Compounds

Ei-ichi Negishi and Pd(II) Compounds without Carbon-Palladium Bonds

Energetic tritium and carbon atoms, reactions of, with organic compounds

Families of Carbon Compounds Functional Groups, Intermolecular Forces, and Infrared (IR) Spectroscopy

Hydrocarbon A compound of carbon and

Hydrocarbon A compound of carbon and hydrogen

Hydrocarbon A compound that contains only carbon and hydrogen

Hydrocarbon An organic compound that contains only carbon and

Hydrocarbons Are Organic Compounds Containing Only Hydrogen and Carbon

Hydrocarbons Compounds Containing Only Carbon and Hydrogen

Hydrocarbons Organic compounds that contain only carbon and hydrogen

Insertion Reactions of Transition Metal-Carbon cr-Bonded Compounds. II. Sulfur Dioxide and Other Molecules

Intercalation Compounds and Endohedral Functionalization of Carbon Nanotubes

Organic Compounds and the Atomic Properties of Carbon

REACTIONS OF HALOGEN COMPOUNDS WITH NITRIC OXIDE AND CARBON MONOXIDE

Reactions at the a Carbon of Carbonyl Compounds Enols and Enolates

Removal of Sulfur Compounds and Carbon Dioxide

Some common acyclic carbon compounds and their uses

Starch and Sucrose Provide the Carbon Skeletons of All Plant Compounds

Synthesis of Alkylamines and Related Compounds through Nitrogen-Carbon(sp3) Bond-Forming Reactions

Synthesis of Ynamides and Related Compounds through Nitrogen-Carbon(sp) Bond-Forming Reactions

What is meant by saturated and unsaturated carbon compounds

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