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  2. Cation–π interaction - Wikipedia

    en.wikipedia.org/wiki/Cation–π_interaction

    Benzene, the model π system, has no permanent dipole moment, as the contributions of the weakly polar carbonhydrogen bonds cancel due to molecular symmetry.However, the electron-rich π system above and below the benzene ring hosts a partial negative charge.

  3. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    The value of α is the energy of an electron in a 2p orbital, relative to an unbound electron at infinity. This quantity is negative, since the electron is stabilized by being electrostatically bound to the positively charged nucleus. For carbon this value is known to be approximately –11.4 eV.

  4. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    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 ...

  5. Sigma complex - Wikipedia

    en.wikipedia.org/wiki/Sigma_complex

    In the halogenation of benzene, the sigma complex comprises the six carbon atoms of the benzene ring, each bonded to a hydrogen atom. An additional halogen atom is bonded to one of the carbon atoms, which is sp 3-hybridized, while the other carbons remain sp 2-hybridized.

  6. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    One electron forms a sigma bond with the hydrogen atom, and one is used in covalently bonding to each of the two neighboring carbons. This leaves six electrons, shared equally around the ring in delocalized pi molecular orbitals the size of the ring itself. [5] This represents the equivalent nature of the six carbon-carbon bonds all of bond order 1

  7. Pi-interaction - Wikipedia

    en.wikipedia.org/wiki/Pi-interaction

    In chemistry, π-effects or π-interactions are a type of non-covalent interaction that involves π systems.Just like in an electrostatic interaction where a region of negative charge interacts with a positive charge, the electron-rich π system can interact with a metal (cationic or neutral), an anion, another molecule and even another π system. [1]

  8. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    Many simple aromatic rings have trivial names. They are usually found as substructures of more complex molecules ("substituted aromatics"). Typical simple aromatic compounds are benzene, indole, and pyridine. [1] [2] Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur.

  9. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is an organic chemical compound with the molecular formula C 6 H 6. The benzene molecule is composed of six carbon atoms joined in a planar hexagonal ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon.

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