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Bond graphs are multi-energy domain (e.g. mechanical, electrical, hydraulic, etc.) and domain neutral. This means a bond graph can incorporate multiple domains seamlessly. The bond graph is composed of the "bonds" which link together "single-port", "double-port" and "multi-port" elements (see below for details).
Another shorthand structural diagram is the skeletal formula (also known as a bond-line formula or carbon skeleton diagram). In a skeletal formula, carbon atoms are not signified by the symbol C but by the vertices of the lines. Hydrogen atoms bonded to carbon are not shown—they can be inferred by counting the number of bonds to a particular ...
A chemical graph is a labeled graph whose vertices correspond to the atoms of the compound and edges correspond to chemical bonds. Its vertices are labeled with the kinds of the corresponding atoms and edges are labeled with the types of bonds. [1] For particular purposes any of the labelings may be ignored. A hydrogen-depleted molecular graph ...
A structural formula is a simplified model that cannot represent certain aspects of chemical structures. For example, formalized bonding may not be applicable to dynamic systems such as delocalized bonds. Aromaticity is such a case and relies on convention to represent the bonding. Different styles of structural formulas may represent ...
A bond of higher bond order also exerts greater repulsion since the pi bond electrons contribute. [10] For example in isobutylene, (H 3 C) 2 C=CH 2, the H 3 C−C=C angle (124°) is larger than the H 3 C−C−CH 3 angle (111.5°). However, in the carbonate ion, CO 2− 3, all three C−O bonds are equivalent with angles of 120° due to resonance.
The skeletal formula of the antidepressant drug escitalopram, featuring skeletal representations of heteroatoms, a triple bond, phenyl groups and stereochemistry. The skeletal formula, line-angle formula, bond-line formula or shorthand formula of an organic compound is a type of molecular structural formula that serves as a shorthand representation of a molecule's bonding and some details of ...
An organic example is tetrahedrane (C 4 H 4) with four carbon atoms each bonded to one hydrogen and the other three carbons. In this case the theoretical C−C−C bond angle is just 60° (in practice the angle will be larger due to bent bonds), representing a large degree of strain. [citation needed]
The ionization of alkanes weakens the C-C bond, ultimately resulting in the decomposition. [7] As the bond breaks, a charged, even electron species (R+) and a neutral radical species (R•) are generated. Highly substituted carbocations are more stable than the nonsubstituted ones. An example is depicted below. Sigma bond cleavage of an alkane.