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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 ...
Hückel's rule can also be applied to molecules containing other atoms such as nitrogen or oxygen. For example pyridine (C 5 H 5 N) has a ring structure similar to benzene, except that one -CH- group is replaced by a nitrogen atom with no hydrogen. There are still six π electrons and the pyridine molecule is also aromatic and known for its ...
Two hydrogen atoms bonded to one carbon lie in a plane perpendicular to the benzene ring. [4] The arenium ion is no longer an aromatic species; however it is relatively stable due to delocalization: the positive charge is delocalized over 3 carbon atoms by the pi system, as depicted on the following resonance structures:
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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.
Printable version; In other projects Wikidata item; Appearance. move to sidebar hide. Resonance structures of benzene 1,2,3-Cyclohexatriene. Cyclohexatriene may refer ...
Similar to these other non-covalent bonds, cation–π interactions play an important role in nature, particularly in protein structure, molecular recognition and enzyme catalysis. The effect has also been observed and put to use in synthetic systems. [1] [2] The π system above and below the benzene ring leads to a quadrupole charge distribution.
For instance, it is argued that the resonance energy measured experimentally via heats of hydrogenation is diminished by the distortions in bond lengths that must take place going from the single and double bonds of "non-aromatic 1,3,5-cyclohexatriene" to the delocalized bonds of benzene.