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The C−H bond in general is very strong, so it is relatively unreactive. In several compound classes, collectively called carbon acids, the C−H bond can be sufficiently acidic for proton removal. Unactivated C−H bonds are found in alkanes and are not adjacent to a heteroatom (O, N, Si, etc.).
Solids with purely metallic bonding are characteristically ductile and, in their pure forms, have low strength; melting points can [inconsistent] be very low (e.g., Mercury melts at 234 K (−39 °C). These properties are consequences of the non-directional and non-polar nature of metallic bonding, which allows atoms (and planes of atoms in a ...
However, C–C bond activation is challenging mainly for the following reasons: (1) C-H bond activation is a competitive process of C-C activation, which is both energetically and kinetically more favorable; (2) the accessibility of the transition metal center to C–C bonds is generally difficult due to its 'hidden' nature; (3) relatively high ...
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.
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.
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.
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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]