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Other Carbons

This is a relatively rare structure, diamond being probably the best known example. Here, the carbon atoms are not close-packed. Each carbon is surrounded tetrahedrally by four other carbon atoms (Figure 2.1). Clearly, each carbon is exerting a tetrahedrally directed... [Pg.26]

These numbers carry other chemical information. For example, z - h = x gives the oxidation state of a carbon atom. In effect, each carbon atom is classified according to its oxidation state, x, and its attachment to other carbon atoms. [Pg.184]

Carbon can also form multiple bonds with other carbon atoms. This results in unsaturated hydrocarbons such as olefins (alkenes), containing a carbon-carbon double bond, or acetylenes (alkynes), containing a carbon-carbon triple bond. Dienes and polyenes contain two or more unsaturated bonds. [Pg.127]

Formation of ketones. Ketones can be prepared by the carbonylation of halides and pseudo-halides in the presence of various organometallic compounds of Zn, B, Al, Sn, Si, and Hg, and other carbon nucleophiles, which attack acylpalladium intermediates (transmetallation and reductive elimination). [Pg.200]

Carbon atoms are classified according to their degree of substitution by other car bons A primary carbon is directly attached to one other carbon Similarly a secondary carbon is directly attached to two other carbons a tertiary carbon to three and a qua ternary carbon to four Alkyl groups are designated as primary secondary or tertiary according to the degree of substitution of the carbon at the potential point of attachment... [Pg.74]

An isopropyl group is a secondary alkyl group Its point of attachment is to a second ary carbon atom one that is directly bonded to two other carbons... [Pg.74]

In the staggered conformation each C—H bond of one carbon bisects an H—C—H angle of the other carbon... [Pg.105]

FIGURE 7 16 Poly mers of propene The mam chain IS shown in a zigzag conformation Every other carbon bears a methyl sub stituent and is a chirality center (a) All the methyl groups are on the same side of the carbon chain in isotactic polypropylene (b) Methyl groups alternate from one side to the other in syndiotactic polypropy lene (c) The spatial orienta tion of the methyl groups IS random in atactic polypropylene... [Pg.313]

Of the sp hybridized carbons C 1 is the most shielded because it is bonded to only one other carbon The least shielded carbon is the ring carbon to which the side chain is attached It is the only sp hybridized carbon connected to three others... [Pg.550]

Like other carbon-carbon bond forming reactions organocuprate addition to enones is a powerful tool m organic synthesis... [Pg.780]

When the compound shown was heated in refluxing aqueous hydrochlonc acid for 60 hours a product with the molecular formula C5H6O3 was isolated in 97% yield Identify this product Along with this product three other carbon containing substances are formed What are they" ... [Pg.912]

Primary carbon (Section 2 13) A carbon that is directly at tached to only one other carbon Primary structure (Section 27 8) The sequence of ammo acids in a peptide or protein... [Pg.1291]

Quaternary carbon (Section 2 13) A carbon that is directly at tached to four other carbons... [Pg.1292]

As a class of compounds, the two main toxicity concerns for nitriles are acute lethality and osteolathyrsm. A comprehensive review of the toxicity of nitriles, including detailed discussion of biochemical mechanisms of toxicity and stmcture-activity relationships, is available (12). Nitriles vary broadly in their abiUty to cause acute lethaUty and subde differences in stmcture can greatly affect toxic potency. The biochemical basis of their acute toxicity is related to their metaboHsm in the body. Following exposure and absorption, nitriles are metabolized by cytochrome p450 enzymes in the Hver. The metaboHsm involves initial hydrogen abstraction resulting in the formation of a carbon radical, followed by hydroxylation of the carbon radical. MetaboHsm at the carbon atom adjacent (alpha) to the cyano group would yield a cyanohydrin metaboHte, which decomposes readily in the body to produce cyanide. Hydroxylation at other carbon positions in the nitrile does not result in cyanide release. [Pg.218]

Plastics. The fastest-growing use of whiting (microcarbonate fillers) is in the plastics industry where dry, pulverized limestone is used intensively for most types of plastics. Other carbonate fillers, precipitated calcium carbonate, oyster sheU, marble, and wet-ground limestone, are also used. [Pg.178]

Cyclopentadienyltitanium Compounds with Other Carbon Titanium Links. Cyclopentadienyltitanium trichloride and, particularly, CpgTiClg react with RLi or with RAl compounds to form one or more R—Ti bonds. As noted, the Cp groups stabilize the Ti—R bond considerably against thermal decomposition, although the sensitivity to air and moisture remains. Depending on the temperature, mole ratio, and stmcture of R, reduction of Ti(IV) may be a serious side reaction, which often has preparative value for Cp Ti(Ill) compounds (268,274,275). [Pg.158]

Molecular Structure and Monomer Addition Orientation. The addition of vinyl monomer to a growing PVC chain can be considered to add in a head-to-tail fashion, resulting in a chlorine atom on every other carbon atom, ie,... [Pg.500]

Trialkylacetic acids have been produced commercially siace the early 1960s, ia the United States by Exxon and ia Europe by Shell, and have been marketed as neo acids (Exxon) or as Versatic Acids (Shell). The principal commercial products are the acid and the C q acid (neodecanoic acid, or Versatic 10), although smaller quantities of other carbon numbers, such as C, C, and C, are also produced. [Pg.102]

Carbon black from oil is the main competition for the product from coal, which is used in filters. Carbon for electrodes is primarily made from petroleum coke, although pitch coke is used in Germany for this product. The pitch binder used for electrodes and other carbon products is almost always a selected coal tar pitch. [Pg.237]

Other carbon electrophiles which are frequently employed include aldehydes, ketones, esters, nitriles and amides of the type RCONMei. An indirect method of acylation involves the initial reaction of a lithio compound with an aldehyde followed by oxidation of the resulting secondary alcohol to the corresponding acyl derivative. [Pg.80]

AU other carbon steel, low-intermediate, and high-aUoy steels, ferritic steels Base metal Deposited weld metal and heat-affected zone (See Note 1) 2. Except when conchtions conform to Note 2, the material shall be heat-treated to control its microstructure by a method appropriate to the material as outlined in the specification applicable to the product form and then impact-tested. (See Note 1.) Deposited weld metal and heat-affected zone shall be impact-tested. [Pg.1006]


See other pages where Other Carbons is mentioned: [Pg.231]    [Pg.56]    [Pg.236]    [Pg.127]    [Pg.3]    [Pg.12]    [Pg.75]    [Pg.114]    [Pg.194]    [Pg.436]    [Pg.558]    [Pg.4]    [Pg.6]    [Pg.127]    [Pg.449]    [Pg.342]    [Pg.432]    [Pg.495]    [Pg.495]    [Pg.497]    [Pg.498]    [Pg.242]    [Pg.289]    [Pg.260]    [Pg.36]    [Pg.394]    [Pg.1820]   


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Acylation at nucleophilic carbon (other than enols and enolates)

Acylation of Enolates and Other Carbon Nucleophiles

Addition of Other Carbon Radicals

Alkylation of Enolates and Other Carbon Nucleophiles

Avoiding Greenhouse Gases Other than Carbon Dioxide

Beta-eliminations giving multiple bonds between carbon and other ELEMENTS

Biosynthesis from Other Single-Carbon Compounds

Calcium carbonate and other additives

Calcium carbonate and other fillers

Carbon monoxide other catalysts

Carbon monoxide other planes

Catenation elements other than carbon

Chirality Centers Other Than Carbon

Chirality at Atoms Other Than Carbon

Chirality centers compounds other than carbon with

Compounds with stereocentres other than carbon

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

Conversion into Other Forms of Carbon

Cyanides and Other Carbon-Nitrogen Compounds

Electrophilic Centers Other than Carbon

Elements Other Than Carbon, Hydrogen, or Oxygen

Enantioselective Conjugate Additions of Enolates and other Stabilized Carbon Nucleophiles

Enolate and Other Carbon Nucleophiles

Fluorine bonded to an element other than carbon

Formation of metal-carbon bonds by other insertion reactions

Heteroatoms Atoms other than carbon

Heteroatoms Atoms other than carbon hydrogen

Hydrogen Attached to Elements Other than Carbon

Inductive Heating of Graphite and Other Carbon Sources

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

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY PART TWO CARBON-13 SPECTRA, INCLUDING HETERONUCLEAR COUPLING WITH OTHER NUCLEI

Nucleophilic Displacements on Atoms Other than Carbon

Nucleophilic aliphatic at elements other than carbon

OTHER FORMS OF CARBON AND GRAPHITE

Other 1-Carbon Cumulenes

Other Applications of Carbon in Fission Reactors

Other Carbon Compounds

Other Carbon Dihalides

Other Carbon Layered Materials

Other Carbon Materials

Other Carbon Nucleophiles

Other Carbon Products

Other Carbon Rearrangements

Other Carbon-Based Conductive Fillers

Other Carbon-Based Fuel Gases

Other Carbon-Centered Radicals

Other Carbon-Heteroatom Multiple Bonds

Other Carbon-bonded Compounds

Other Carbon-bonded Derivatives

Other Carbonates

Other Cascades Initiated by Michael Reactions Using Stabilized Carbon Nucleophiles

Other Flexible Carbon-Backbone Macromolecules

Other Forms of Carbon

Other Four-Carbon Annulations

Other Group IIA carbonates

Other Molecules with Possibly Pyramidal Carbon

Other Nucleophilic Carbon Species

Other One-Carbon Homologation Reactions

Other One-Carbon Unit Equivalents

Other Polymers with Saturated Carbon Chain Backbone

Other Processing - Molten Carbonate Method

Other Reactions at the Carbonyl Carbon Atom

Other Reactions of Carbon Monoxide

Other Sources of One-Carbon Substituted Folates

Other Types of Carbon-centred Radicals

Other aerospace applications of carbon nanotubes

Other carbon-linked functionality

Other examples of carbon determinations in non-ferrous metals

Other molecular allotropes of carbon

Other perethynylated compounds as potential monomers for carbon networks

Other planar lattices with -hybridized carbon

Other systems with -hybridized carbon atoms

Oxidation of carbon monoxide in flames and other high temperature flow systems

Prediction of Carbon Shifts and their Correlation with Other Physicochemical Parameters

Pyridine and other molecules containing five carbon atoms

Reactions at Other Carbon-linked Groups

Reactions of Carbonyl Compounds with Other Carbon Nucleophiles

Reactions with Other Carbon Nucleophiles

Replacement of Carbon by Other Elements

Satellites from Carbon-13 and Other Nuclides

Stereogenic Centers Other Than Carbon

The effects of elevated carbon dioxide levels on global temperature and other properties

Triosmium Clusters with Group IV Elements Other than Carbon

Use of Activated Carbon in Conjunction with other Separations

Vibrations of Methyl Groups Attached to Elements other than Carbon

Water-to-Air Fluxes of Carbon Dioxide and Other Dissolved Gases in Estuaries

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