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  2. 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 ...

  3. 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 ...

  4. 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 ...

  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. Negative hyperconjugation in silicon - Wikipedia

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

    Negative hyperconjugation is a theorized phenomenon in organosilicon compounds, in which hyperconjugation stabilizes or destabilizes certain accumulations of positive charge. The phenomenon explains corresponding peculiarities in the stereochemistry and rate of hydrolysis .

  7. Zaytsev's rule - Wikipedia

    en.wikipedia.org/wiki/Zaytsev's_rule

    Based on this trend, Zaytsev proposed that the alkene formed in greatest amount is that which corresponded to removal of the hydrogen from the alpha-carbon having the fewest hydrogen substituents. For example, when 2-iodobutane is treated with alcoholic potassium hydroxide (KOH), but-2-ene is the major product and but-1-ene is the minor product.

  8. Hydrogen atom abstraction - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_atom_abstraction

    The entity removing the hydrogen atom, known as the abstractor (X•), is often a radical itself, though in some instances, it may be a species with a closed electron shell, such as chromyl chloride. Hydrogen atom transfer can occur via a mechanism known as proton-coupled electron transfer.

  9. 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.

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