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Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.
Bonding in the cyano radical can be described as a combination of two resonance structures: the structure with the unpaired electron on the carbon is the minor contributor, while the structure with the unpaired electron on the nitrogen (the isocyano radical) is the major contributor.
Operationally, there are three ways in which alternative resonance structures may be generated: (1) from the LEWIS option, considering the Wiberg bond indices; (2) from the delocalization list; (3) specified by the user. [1] Below is an example of how NRT may generate a list of resonance structures.
Clar's rule states that for a benzenoid polycyclic aromatic hydrocarbon (i.e. one with only hexagonal rings), the resonance structure with the largest number of disjoint aromatic π-sextets is the most important to characterize its chemical and physical properties. Such a resonance structure is called a Clar structure. In other words, a ...
One of the simplest member is C(CN) 4 (tetracyanomethane, also known as carbon tetracyanide). Organic chemists often refer to cyanides as nitriles. In general, cyanide is an electronegative substituent. Thus, for example, cyanide-substituted carboxylic acids tend to be stronger than the parents.
According to the Washington Research Council, the latest update on the 2025-2027 budget shortfall puts the figure at $4.8 billion. If Inslee’s $16 billion figure were accurate, it would leave ...
A blast of Arctic air taking over much of the U.S. this weekend is bringing powerful lake-effect snow to several states, including Pennsylvania and New York, and shivering temperatures to parts of ...
4-Cyano-4'-pentylbiphenyl is a commonly used nematic liquid crystal with the chemical formula C 18 H 19 N. It frequently goes by the common name 5CB. 5CB was first synthesized by George William Gray, Ken Harrison, and J.A. Nash at the University of Hull in 1972 and at the time it was the first member of the cyanobiphenyls.