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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.
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 ...
The Taipei 101 building relies on a 660-tonne pendulum (730-short-ton)—a tuned mass damper—to cancel resonance. Furthermore, the structure is designed to resonate at a frequency that does not typically occur. Buildings in seismic zones are often constructed to take into account the oscillating frequencies of expected ground motion.
Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure ...
When one electron is removed from an sp 3 orbital, resonance is invoked between four valence bond structures, each of which has a single one-electron bond and three two-electron bonds. Triply degenerate T 2 and A 1 ionized states (CH 4 +) are produced from different linear combinations of these four structures. The difference in energy between ...
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]
The structure of an amide can be described also as a resonance between two alternative structures: neutral (A) and zwitterionic (B). It is estimated that for acetamide , structure A makes a 62% contribution to the structure, while structure B makes a 28% contribution (these figures do not sum to 100% because there are additional less-important ...
Diazo compounds have two main Lewis structures in resonance: R 2 >C-–N + ≡N and R 2 >CH=N + =N-. In organic chemistry, the diazo group is an organic moiety consisting of two linked nitrogen atoms at the terminal position.