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Methane carbon-hydrogen bond

Oxidation of carbon corresponds to an increase in the number of bonds between carbon and oxygen or to a decrease in the number of carbon-hydrogen bonds Conversely reduction corresponds to an increase in the number of carbon-hydrogen bonds or to a decrease in the number of carbon-oxygen bonds From Table 2 4 it can be seen that each successive increase m oxidation state increases the number of bonds between carbon and oxygen and decreases the number of carbon-hydrogen bonds Methane has four C—H bonds and no C—O bonds car bon dioxide has four C—O bonds and no C—H bonds... [Pg.87]

From Table 2.4 it can be seen that each successive increase in oxidation state increases the number of bonds between carbon and oxygen and decreases the number of carbon-hydrogen bonds. Methane has four C—H bonds and no C—O bonds carbon dioxide has four C—O bonds and no C—H bonds. [Pg.84]

Finally, the change in selectivity for the methane/pentane couple for the two different substrates (18% for hexane, 56% for cyclohexane) can be explained as follows in the case of cyclohexane, the Ci to C5 products are formed through the second carbon-carbon bond cleavage via the hexyl surface intermediate D whereas in the case of hexane, the initial carbon-hydrogen bond activation step can lead to any of three alkyl surface intermediates (D, E, and F) before arriving at the key metallacychc intermediates... [Pg.198]

Example In methane (CH4) the four covalent carbon-hydrogen bonds are of different strength ... [Pg.67]

The molecular geometry of methane and of methyl fluoride is tetrahedral. In the case of methane, this symmetrical arrangement of polar covalent carbon-hydrogen bonds leads to a canceling of the bond polarities resulting in a nonpolar molecule. As a nonpolar molecule, the strongest intermolecular force in methane is a London force. In methyl fluoride, a fluorine atom replaces one of the hydrogen... [Pg.166]

This value of the C-H bond enthalpy does not correspond to the enthalpy of dissociation of the carbon-hydrogen bond in methane, as represented in Equation (4.35). [Pg.58]

In this section, we shall examine the results which have been obtained for the exchange of the saturated hydrocarbons methane, ethane, cyclopentane, cyclohexane, cycloheptane, cyclo-octane, and neopentane. The common characteristic of this group is that all the carbon-hydrogen bonds in each individual molecule are similar in nature. An attempt will be made to indicate how the results fit into the classifications outlined in Sec. II. [Pg.239]

Alkanes have only -hybridized carbons. The conformation of alkanes is discussed in Chapter 3 (see Section 3.2.2). Methane (CH4) is a nonpolar molecule, and has four covalent carbon-hydrogen bonds. In methane, aU four C—H bonds have the same length (1.10 A), and all the bond angles (109.5°) are the same. Therefore, all four covalent bonds in methane are identical. Three different ways to represent a methane molecule are shown here. In a perspective formula, bonds in the plane of the paper are drawn as solid hues, bonds sticking out of the plane of the paper towards you are... [Pg.64]

Burger. P. and Bergman, R.G. (1993) Facile intermolecular activation of carbon-hydrogen bonds in methane and other hydrocarbons and silicon-hydrogen bonds in silanes with the iridium(III) complex Cp (PMe3)Ir (CH3)(OTf). J. Am. Chem. Soc., 115 (22). 10462-10463. [Pg.194]

Under pyrolytic conditions at temperatures above 300°C, generally within 500-800°C, the pyrolysis reaction forms alkenes by carbon-hydrogen bond scissions. An early experiment, where propane was heated to 575°C for 4 min in a silica flask, yielded propylene by dehydrogenation [Eqs. (2.19)-(2.21)] at a somewhat slower rate than it yielded methane and ethylene by cracking 54... [Pg.45]

Carbon-hydrogen bonds, such as those in hydrocarbons like methane and ethane, have dissociation energies close to 400 kj-mol whereas single bonds between carbon and fluorine have dissociation energies close to 500 kj-mol-1. The greater strength of a carbon-fluorine bond helps to explain why fluorocarbon polymers are very resistant to chemical attack. They are used to construct valves for corrosive gases and to line the interiors of chemical reactors. [Pg.229]

What is the bond angle between the carbon atom and a hydrogen atom in the methane molecule Is this angle the same for all the carbon-hydrogen bonds in methane ... [Pg.209]

The correct answer is (D). According to electron configuration of carbon, the carbon atom should have two electrons in the 2s orbital and one in each of the two 2p orbitals. The four carbon-hydrogen bonds in methane should be different because of the different orbitals, yet experimental evidence shows them to be the same. The solution is that one... [Pg.499]

Inside a covalent molecule, the covalent bonds are directed in space at specific angles. In the case of the methane molecule the carbon-hydrogen bonds are at 109.5°, in other words towards the comers of a tetrahedron with the carbon atom at its centre (Figure 2.9). [Pg.23]

This established C-H chemistry in molecular coordination compounds should have its formal analog in metal surface chemistry. Carbon-hydrogen bond-cleavage is a common reaction at metal surfaces but it does not comprise mechanistically the simple collision of a hydrocarbon such as methane with a metal surface vide infra). Methane neither reacts with nor is chemisorbed on a metal surface under moderate conditions. However, propylene does chemisorb, and then C-H bonds may be broken, depending upon the nature of the metal surface. Generally, the sequence at the surface comprises first the formation of a coordinate bond between a surface metal atom(s) and some functionality in the... [Pg.274]

Some of the first catalytic model systems for the simulation of the function of methane monooxygenase comprise monomeric as well as dimeric iron-containing model complexes bearing hydro-tris(pyrazolyl)borate ligands [6]. These complexes, e.g. 3, catalyze the oxidation of aromatic and aliphatic carbon-hydrogen bonds in the presence of oxygen (1 atm), acetic acid and zinc powder at room temperature (Scheme 2). [Pg.188]


See other pages where Methane carbon-hydrogen bond is mentioned: [Pg.18]    [Pg.18]    [Pg.66]    [Pg.182]    [Pg.292]    [Pg.654]    [Pg.151]    [Pg.92]    [Pg.93]    [Pg.151]    [Pg.264]    [Pg.913]    [Pg.66]    [Pg.167]    [Pg.5]    [Pg.57]    [Pg.67]    [Pg.244]    [Pg.154]    [Pg.578]    [Pg.212]    [Pg.66]    [Pg.31]    [Pg.2]    [Pg.353]    [Pg.179]    [Pg.143]    [Pg.147]    [Pg.182]    [Pg.69]   


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