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  2. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    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.

  3. Orbital resonance - Wikipedia

    en.wikipedia.org/wiki/Orbital_resonance

    A binary resonance ratio in this article should be interpreted as the ratio of number of orbits completed in the same time interval, rather than as the ratio of orbital periods, which would be the inverse ratio. Thus, the 2:3 ratio above means that Pluto completes two orbits in the time it takes Neptune to complete three.

  4. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    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 ]

  5. Hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Hyperconjugation

    In organic chemistry, hyperconjugation (σ-conjugation or no-bond resonance) refers to the delocalization of electrons with the participation of bonds of primarily σ-character. Usually, hyperconjugation involves the interaction of the electrons in a sigma (σ) orbital (e.g. C–H or C–C) with an adjacent unpopulated non-bonding p or ...

  6. Delocalized electron - Wikipedia

    en.wikipedia.org/wiki/Delocalized_electron

    In chemistry, delocalized electrons are electrons in a molecule, ion or solid metal that are not associated with a single atom or a covalent bond. [1] The term delocalization is general and can have slightly different meanings in different fields: In organic chemistry, it refers to resonance in conjugated systems and aromatic compounds.

  7. Stereoelectronic effect - Wikipedia

    en.wikipedia.org/wiki/Stereoelectronic_effect

    Founded on a few general principles that govern how orbitals interact, the stereoelectronic effect, along with the steric effect, inductive effect, solvent effect, mesomeric effect, and aromaticity, is an important type of explanation for observed patterns of selectivity, reactivity, and stability in organic chemistry. In spite of the ...

  8. Molecular orbital - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital

    In chemistry, a molecular orbital (/ ɒr b ə d l /) is a mathematical function describing the location and wave-like behavior of an electron in a molecule. This function can be used to calculate chemical and physical properties such as the probability of finding an electron in any specific region.

  9. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    This is a weighted sum of the wavefunctions. Now choose a second hybrid orbital s + √ λ j p j, where p j is directed in some way and λ j is the amount of p character in this second orbital. The value of λ j and direction of p j must be determined so that the resulting orbital can be normalized and so that it is orthogonal to the first ...