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Oxidation carbon atom

The TCA cycle. In each turn of the cycle, acetyl-CoA from the glycolytic pathway or from /3 oxidation of fatty acids enters and two fully oxidized carbon atoms leave (as C02). ATP is generated at one point in the cycle, and coenzyme molecules are reduced. The two C02 molecules lost in each cycle originate from the oxaloacetate of the previous cycle rather than from incoming acetyl from acetyl-CoA. This point is emphasized by the use of color. [Pg.286]

An entirely different approach to unsaturated acyclic derivatives involves the generation of the multiple bonds by use of Wittig-like processes applied to aldehyde substrates with the oxidized carbon atom at either terminus of the carbon chain. Furthermore, the aldehydic moieties may be masked in... [Pg.105]

DMD is suitable for the oxidation of most substrates with substances that are resistant to oxidation, however, the more reactive but also more expensive methyl (trifluoromethyl)dioxirane (TFD) is necessary. The oxidation is stereoselective for both dioxiranes and proceeds with complete retention of configuration at the oxidized carbon atom (Scheme 1) [20-22]. The reactivity follows the usual order of electrophilic oxidation-primary < secondary < tertiary < benzylic < allylic C-H bonds. Except for tertiary C-H bonds, which produce the oxidatively inert tertiary alcohols, further oxidation of the primary product (an alcohol) to a ketone or aldehyde (the latter is readily further oxidized to the corresponding acid) is possible, because the a-hydrogen of the alcohol is usually more reactive than that of the unactivated alkane, especially for allylic C-H bonds. [Pg.508]

Hie highest with substrates containing two such groups. The reaction of configuration at the oxidized carbon atom, used for a one-pot conversion of a terminal alkene into the anti-ty a hydrosilylation-oxidation sequence (equation II). ... [Pg.243]

Benzoin can be oxidized to the a-diketone, benzii, very efficiently by nitric acid or by copper(II) sulfate in pyridine. On oxidation with sodium dichromate in acetic acid the yield is lower because some material is converted into benzaldehyde by cleavage of the bond between two oxidized carbon atoms and activated by both phenyl groups (a). Similarly, hydrobenzoin on oxidation with dichromate or permanganate yields chiefly benzaldehyde and only a trace of benzii (b). [Pg.471]

Methane interacts with the surface by the di.spersion mechanism. In doing so, it can adsorb in micropores as well as on oxidized carbon atoms and positions of junction of graphene planes. The maximum value of 8 — 8o for methane is —6 ppm, which is by 3 ppm smaller than for water. On the assumption that graphene-plane micropores affect the chemical shifts for any adsorbed molecules in the same way, it is possible to draw a conclusion that the micropores contain about 2/3 of all the adsorbed methane molecules. [Pg.94]

As is seen from the data in Table 4, upon treatment of the carbon surface with hydrogen, the value of its free surface energy sharply decreases. This agrees with the notion that such a treatment results in a decrease in the surface concentration of oxidized carbon atoms that form hydrogen-bonded complexes with water molecules. Besides, a sharp decrease in the concentration of water in the adsorbent micropores is also observed. This effect can be explained by lower accessibility of micropores for water molecules caused by deteriorating hydrophilic properties of the adsorbent surface. When a carbon surface is treated with hydrogen peroxide, we observe an increase in the bound water concentration at the expense of the creation of new oxidized sites that would form hydrogen-bonded complexes with water molecules. [Pg.97]

Further action results in the chlorination of the alpha carbon atom, producing trichloroacetaldehyde, or chloral, CI3C—CHO. This compound, having two partially oxidized carbon atoms, on warming undergoes a rupture of the carbon-to-carbon bond ... [Pg.197]

The mixed-function oxidase system also oxidizes carbon atoms adjacent (i.e.. a) to carbonyl and imino (C = N) func-linnalitics. An important class of drugs undergoing this type of oxidation is the benzodiazepines. For example, diazepam IValiumI, flurazepam (Dalmane), and nimetazepam are oxi-Ji/ed to their corresponding 3-hydroxy metabolites. [Pg.81]

Ans. The d-l nomenclature system applies only for the case of a stereocenter attached to two different carbon substituents R and R, a hydrogen, and a hetero atom substituent X (e.g., OH or NH,)- The molecule is drawn so that the R and R substituents are vertical while the H and hetero atom substituents are horizontal. R, the carbon substituent which has the most highly oxidized carbon atom (the carbon with the least number of hydrogens) attached to the stereocenter, is placed up. The enantiomer with the X substituent on the right-hand side is the D-enantiomer while that with the X substituent on the left-hand side is the L-enantiomer ... [Pg.339]

Of the 18 carbon atoms in a saturated fatty acid, 17 are saturated (as —CH2— groups) and are more reduced than the partially oxidized carbon atoms in glucose. In glucose, five of the six carbons are partially oxidized to the hydroxymethyl level, and the sixth is at the more oxidized aldehyde level. A greater number of electrons per carbon are available in the fatty acid, so more metabolic energy is available from it than from glucose. [Pg.240]

It is convenient in employing the Fischer convention to use projection formulas. These Fischer projections are obtained by orienting the molecule so that the most highly oxidized carbon atom of the main chain is at the top, with the vertical bonds from the asymmetric carbon atom directed back and the horizontal bonds directed forward. The d and l forms of glyceraldehyde then become as shown in the following three-dimensional representations and Fischer projection formulas ... [Pg.42]

The particle surface has the shape of a curved staircase formed by overlapped crystallites. In the case of both of the types of carbon black particles on the boundaries of crystallites, there can be a great number of hydrogen atoms, oxidized carbon atoms, and broken carbon bonds. Atom force microscopy (AFM) images of carbon black (Tanahashi et al. 1990, Donnet 1994) showed that crystallites are presented on the surface and they have the form of rectangles, but their arrangement can be random. It is evident that the differences in the carbon black particle structure observed by various techniques for diverse materials reflect the diversity of synthesized carbonaceous materials... [Pg.458]

On the amorphous carbon surface, such water adsorption sites are oxidized carbon atoms. Their concentration is usually much lower than that of hydroxyl groups on the silica surface, which should diminish the hydrophilic properties of the silica gel surface during carbonization. In contrast to it, however, there is an increase in the adsorbent hydrophilic properties for the CSG-5 and CSG-6 samples, which manifests itself in the increase of the Ys and C"w values. In the case of the CSG-6 sample, Ys is even higher than for the initial silica gel. The regularities of variations in the hydrophilic... [Pg.553]

In this reaction, the four sulfur atoms and the carbon atoms of the thiocarbonyl groups are oxidized. The sulfur atoms of the disulfide bridge may be considered as passing from oxidation state +I to state +VI, the two others passing from state + II to stated-VI, the oxidized carbon atoms having passed from state - II to state -t II. [Pg.372]

The oxidized carbon atom must be place in the catalytic site aligned along the C-O-O- axis. [Pg.873]


See other pages where Oxidation carbon atom is mentioned: [Pg.407]    [Pg.482]    [Pg.10]    [Pg.449]    [Pg.94]    [Pg.307]    [Pg.243]    [Pg.75]    [Pg.79]    [Pg.94]    [Pg.98]    [Pg.104]    [Pg.113]    [Pg.114]    [Pg.118]    [Pg.591]    [Pg.300]    [Pg.241]    [Pg.48]    [Pg.591]    [Pg.15]    [Pg.856]    [Pg.462]    [Pg.468]    [Pg.546]    [Pg.554]    [Pg.44]    [Pg.96]    [Pg.7]    [Pg.908]    [Pg.909]   
See also in sourсe #XX -- [ Pg.521 ]




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Oxidation of Non-functional Carbon Atoms

Oxidation of hydrocarbons containing four carbon atoms

Oxidations at Unfunctionalized Carbon Atoms

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