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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. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  5. Negative hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Negative_hyperconjugation

    In organic chemistry, negative hyperconjugation is the donation of electron density from a filled π- or p-orbital to a neighboring σ *-orbital. [1] 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]

  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. 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 ...

  8. Alpha effect - Wikipedia

    en.wikipedia.org/wiki/Alpha_effect

    The alpha effect refers to the increased nucleophilicity of an atom due to the presence of an adjacent (alpha) atom with lone pair electrons. [2] This first atom does not necessarily exhibit increased basicity compared with a similar atom without an adjacent electron-donating atom, resulting in a deviation from the classical Brønsted-type ...

  9. Gas exchange - Wikipedia

    en.wikipedia.org/wiki/Gas_exchange

    Gas exchange is the physical process by which gases move passively by diffusion across a surface. For example, this surface might be the air/water interface of a water body, the surface of a gas bubble in a liquid, a gas-permeable membrane, or a biological membrane that forms the boundary between an organism and its extracellular environment.