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  2. Hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Hyperconjugation

    Hyperconjugation can be used to rationalize a variety of chemical phenomena, including the anomeric effect, the gauche effect, the rotational barrier of ethane, the beta-silicon effect, the vibrational frequency of exocyclic carbonyl groups, and the relative stability of substituted carbocations and substituted carbon centred radicals, and the thermodynamic Zaitsev's rule for alkene stability.

  3. Cieplak effect - Wikipedia

    en.wikipedia.org/wiki/Cieplak_Effect

    The Cieplak effect relies on the stabilizing interaction of mixing full and empty orbitals to delocalize electrons, known as hyperconjugation. [2] When the highest occupied molecular orbital of one system and the lowest unoccupied molecular orbital of another system have comparable energies and spatial overlap, the electrons can delocalize and sink into a lower energy level.

  4. Negative hyperconjugation in silicon - Wikipedia

    en.wikipedia.org/wiki/Negative_hyperconjugation...

    The continued presence of second-row type stability in certain organosilicon compounds is known as the silicon α and β effects, after the corresponding locants. These stabilities occur because of a partial overlap between the C–Si σ orbital and the σ* antibonding orbital at the β position, lowering the S N reaction transition state's energy.

  5. Negative hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Negative_hyperconjugation

    This phenomenon, a type of resonance, can stabilize the molecule or transition state. [2] It also causes an elongation of the σ-bond by adding electron density to its antibonding orbital. [1] Negative hyperconjugation is seldom observed, though it can be most commonly observed when the σ *-orbital is located on certain C–F or C–O bonds ...

  6. Anomeric effect - Wikipedia

    en.wikipedia.org/wiki/Anomeric_effect

    The α- and β-anomers of D-glucopyranose.. In organic chemistry, the anomeric effect or Edward-Lemieux effect (after J. T. Edward and Raymond Lemieux) is a stereoelectronic effect that describes the tendency of heteroatomic substituents adjacent to the heteroatom in the ring in, e.g., tetrahydropyran to prefer the axial orientation instead of the less-hindered equatorial orientation that ...

  7. Casimir effect - Wikipedia

    en.wikipedia.org/wiki/Casimir_effect

    The presence of ħ shows that the Casimir force per unit area ⁠ F c / A ⁠ is very small, and that furthermore, the force is inherently of quantum-mechanical origin. By integrating the equation above it is possible to calculate the energy required to separate to infinity the two plates as:

  8. Macroscopic quantum phenomena - Wikipedia

    en.wikipedia.org/wiki/Macroscopic_quantum_phenomena

    Right: a very large number of particles. There is generally a large number of particles in the box. The fluctuations around the average are small compared to the number in the box. The concept of macroscopically occupied quantum states is introduced by Fritz London. [4] [5] In this section it will be explained what it means if a single state is ...

  9. Kinetic isotope effect - Wikipedia

    en.wikipedia.org/wiki/Kinetic_isotope_effect

    A primary kinetic isotope effect (PKIE) may be found when a bond to the isotopically labeled atom is being formed or broken. [3] [4]: 427 Depending on the way a KIE is probed (parallel measurement of rates vs. intermolecular competition vs. intramolecular competition), the observation of a PKIE is indicative of breaking/forming a bond to the isotope at the rate-limiting step, or subsequent ...