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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.
In chemistry, the mesomeric effect (or resonance effect) is a property of substituents or functional groups in a chemical compound.It is defined as the polarity produced in the molecule by the interaction of two pi bonds or between a pi bond and lone pair of electrons present on an adjacent atom. [1]
Resonance can occur in either. "every bond is connecting adjacent atoms" is not true. The 1-4 bond in Dewar structures of benzene can hardly be called connecting adjacent atoms. Another example is the 1-3 long bond in the singlet diradical structure of ozone where there is a massive literature saying that it is important.
This page shows the electron configurations of the neutral gaseous atoms in their ground states. For each atom the subshells are given first in concise form, then with all subshells written out, followed by the number of electrons per shell.
This bonding scheme is succinctly summarized by the following two resonance structures: I—I···I − ↔ I − ···I—I (where "—" represents a single bond and "···" represents a "dummy bond" with formal bond order 0 whose purpose is only to indicate connectivity), which when averaged reproduces the I—I bond order of 0.5 obtained ...
Given a list of NBOs for an idealized natural Lewis structure, the NRT functional creates a list of Lewis resonance structures and calculates the resonance weights of each contributing resonance structure. [1] Structural and chemical properties, such as bond order, valency, and bond polarity, may be calculated from resonance weights. [2]
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 ...
Mesons named with the letter "f" are scalar mesons (as opposed to a pseudo-scalar meson), and mesons named with the letter "a" are axial-vector mesons (as opposed to an ordinary vector meson) a.k.a. an isoscalar vector meson, while the letters "b" and "h" refer to axial-vector mesons with positive parity, negative C-parity, and quantum numbers I G of 1 + and 0 − respectively.