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  2. 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 ...

  3. Hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Hyperconjugation

    A portion of Kistiakowsky's work involved a comparison of other unsaturated compounds in the form of CH 2 =CH(CH 2)n-CH=CH 2 (n=0,1,2). These experiments revealed an important result; when n=0, there is an effect of conjugation to the molecule where the ΔH value is lowered by 3.5 kcal. This is likened to the addition of two alkyl groups into ...

  4. Hydrogen–deuterium exchange - Wikipedia

    en.wikipedia.org/wiki/Hydrogen–deuterium_exchange

    Hydrogen–deuterium exchange (also called H–D or H/D exchange) is a chemical reaction in which a covalently bonded hydrogen atom is replaced by a deuterium atom, or vice versa. It can be applied most easily to exchangeable protons and deuterons, where such a transformation occurs in the presence of a suitable deuterium source, without any ...

  5. Deuterium - Wikipedia

    en.wikipedia.org/wiki/Deuterium

    Deuterium (hydrogen-2, symbol 2 H or D, also known as heavy hydrogen) is one of two stable isotopes of hydrogen; the other is protium, or hydrogen-1, 1 H. The deuterium nucleus (deuteron) contains one proton and one neutron, whereas the far more common 1 H has no neutrons. The name deuterium comes from Greek deuteros, meaning "second".

  6. Electrophilic substitution of unsaturated silanes - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_substitution...

    Halogen electrophiles, primarily X 2, react with vinyl- and allylsilanes to give a number of halogenated products. Further reaction of the initial adducts is common, and may lead, for instance, to conjugated dienes. Dienes may react further with X 2 under the reaction conditions or undergo [4+2] cycloadditions in the presence of dienophiles ...

  7. Hydrogen spectral series - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_spectral_series

    The Balmer series includes the lines due to transitions from an outer orbit n > 2 to the orbit n' = 2. Named after Johann Balmer, who discovered the Balmer formula, an empirical equation to predict the Balmer series, in 1885. Balmer lines are historically referred to as "H-alpha", "H-beta", "H-gamma" and so on, where H is the element hydrogen. [10]

  8. Hydrogen-alpha - Wikipedia

    en.wikipedia.org/wiki/Hydrogen-alpha

    Hydrogen-alpha, typically shortened to H-alpha or Hα, is a deep-red visible spectral line of the hydrogen atom with a wavelength of 656.28 nm in air and 656.46 nm in vacuum. It is the first spectral line in the Balmer series and is emitted when an electron falls from a hydrogen atom's third- to second-lowest energy level.

  9. Enolate - Wikipedia

    en.wikipedia.org/wiki/Enolate

    The alpha hydrogen deprotonated to form the kinetic enolate is less hindered, and therefore deprotonated more quickly. In general, tetrasubstituted olefins are more stable than trisubstituted olefins due to hyperconjugative stabilization. The ratio of enolate regioisomers is heavily influenced by the choice of base.