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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 ...
Pushing a person in a swing is a common example of resonance. The loaded swing, a pendulum, has a natural frequency of oscillation, its resonant frequency, and resists being pushed at a faster or slower rate. A familiar example is a playground swing, which acts as a pendulum. Pushing a person in a swing in time with the natural interval of the ...
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 ...
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]
Example of a dipolar compound, represented by a resonance structure In organic chemistry , a dipolar compound or simply dipole is an electrically neutral molecule carrying a positive and a negative charge in at least one canonical description.
A demonstration that how some well known 1,3-dipoles like ozone, nitro compounds and azides can be shown to have a resonance structure having 1,3 relationship between positive and negative formal charges. Known 1,3-dipoles are: Azides (RN 3) Ozone (O 3) Nitro compounds (RNO 2) Diazo compounds (R 2 CN 2) Some oxides. Azoxide compounds (RN(O)NR)
Resonance Rings exhibit at California Science Center. Various examples of mechanical resonance include: Musical instruments (acoustic resonance). Most clocks keep time by mechanical resonance in a balance wheel, pendulum, or quartz crystal. Tidal resonance of the Bay of Fundy. Orbital resonance, as in some moons of the Solar System's giant planets.