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In chemistry, the carbon–hydrogen bond (C−H bond) is a chemical bond between carbon and hydrogen atoms that can be found in many organic compounds. [1] This bond is a covalent , single bond , meaning that carbon shares its outer valence electrons with up to four hydrogens.
Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.
Compared with β-carbon elimination, oxidative addition of C-C bond is a more direct way of C-C bond activation. However, it is more challenging to do for the following reasons: 1) It forms two weak M-C bonds at the expense of breaking a stable C-C bond, so it is energetically unfavorable; 2) the C-C bond is usually hindered, which makes the ...
An alkane has only C–H and C–C single bonds. The former result from the overlap of an sp 3 orbital of carbon with the 1s orbital of a hydrogen; the latter by the overlap of two sp 3 orbitals on adjacent carbon atoms. The bond lengths amount to 1.09 × 10 −10 m for a C–H bond and 1.54 × 10 −10 m for a C–C bond.
Mellitic acid, which contains no C-H bonds, is considered a possible organic compound in Martian soil. [15] Terrestrially, it, and its anhydride, mellitic anhydride, are associated with the mineral mellite (Al 2 C 6 (COO) 6 ·16H 2 O). A slightly broader definition of the organic compound includes all compounds bearing C-H or C-C bonds.
Transforming C-H bonds into C-B bonds through borylation has been thoroughly investigated due to their utility in synthesis (i.e. for cross-coupling reactions). John F. Hartwig reported a highly regioselective arene and alkane borylation catalyzed by a rhodium complex. In the case of alkanes, exclusive terminal functionalization was observed. [19]
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The π bond between the carbon atoms perpendicular to the molecular plane is formed by 2p–2p overlap. Each carbon atom forms covalent C–H bonds with two hydrogens by s–sp 2 overlap, all with 120° bond angles. The hydrogen–carbon bonds are all of equal strength and length, in agreement with experimental data.