Search results
Results From The WOW.Com Content Network
Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.
Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.
Alternatively to the use of contributing structures in diagrams, a hybrid structure can be used. In a hybrid structure, pi bonds that are involved in resonance are usually pictured as curves [10] or dashed lines, indicating that these are partial rather than normal complete pi bonds. In benzene and other aromatic rings, the delocalized pi ...
The following other wikis use this file: Usage on de.wikibooks.org Organische Chemie für Schüler/ Aromatische Kohlenwasserstoffe; Organische Chemie für Schüler/ Druckversion
[18] [19] The LDQ structure for benzene is shown below. [16] [24] The LDQ structure of benzene. The carbon nuclei are coloured brown and the hydrogen nuclei are coloured pink, while the electrons are coloured either purple or green to distinguish between the spin sets. Left: The dot-and-cross diagram of the LDQ structure of benzene.
The Simplified Molecular Input Line Entry System (SMILES) is a specification in the form of a line notation for describing the structure of chemical species using short ASCII strings. SMILES strings can be imported by most molecule editors for conversion back into two-dimensional drawings or three-dimensional models of the molecules.
The most common Lewis bases are anions. The strength of Lewis basicity correlates with the pK a of the parent acid: acids with high pK a 's give good Lewis bases. As usual, a weaker acid has a stronger conjugate base. Examples of Lewis bases based on the general definition of electron pair donor include: simple anions, such as H − and F −
Antibonding orbitals are often labelled with an asterisk (*) on molecular orbital diagrams. In homonuclear diatomic molecules, σ* (sigma star) antibonding orbitals have no nodal planes passing through the two nuclei, like sigma bonds, and π* (pi star) orbitals have one nodal plane passing through the two nuclei, like pi bonds.