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  2. Negative hyperconjugation in silicon - Wikipedia

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

    The silicon effect also manifests in certain compound properties. Trimethylsilylmethylamine (Me 3 SiCH 2 NH 2) is a stronger base (conjugate pK a 10.96) than neopentylamine (conjugate pK a 10.21); trimethylsilylacetic acid (pKa 5.22) is a poorer acid than trimethylacetic acid (pKa 5.00). [1]

  3. Negative hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Negative_hyperconjugation

    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 ] [ 4 ] In negative hyperconjugation, the electron density flows in the opposite direction (from a π- or p-orbital to an empty σ * -orbital) than it does in the more common ...

  4. Silicone oil - Wikipedia

    en.wikipedia.org/wiki/Silicone_oil

    A silicone oil is any liquid polymerized siloxane with organic side chains. The most important member is polydimethylsiloxane . These polymers are of commercial interest because of their relatively high thermal stability and their lubricating properties.

  5. 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.

  6. Silicon compounds - Wikipedia

    en.wikipedia.org/wiki/Silicon_compounds

    Silicon compounds are compounds containing the element silicon (Si). As a carbon group element, silicon often forms compounds in the +4 oxidation state, though many unusual compounds have been discovered that differ from expectations based on its valence electrons, including the silicides and some silanes. Metal silicides, silicon halides, and ...

  7. Organosilicon chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosilicon_chemistry

    The silicon to hydrogen bond is longer than the C–H bond (148 compared to 105 pm) and weaker (299 compared to 338 kJ/mol). Hydrogen is more electronegative than silicon hence the naming convention of silyl hydrides. Commonly the presence of the hydride is not mentioned in the name of the compound. Triethylsilane has the formula Et 3 SiH.

  8. NTSB: Engine oil warnings sounded moments before jet ... - AOL

    www.aol.com/news/ntsb-engine-oil-warnings...

    Moments before the deadly crash of a charter jet on a Florida highway, three warnings about oil pressure problems in its two engines sounded, the National Transportation Safety Board said in a ...

  9. Sakurai reaction - Wikipedia

    en.wikipedia.org/wiki/Sakurai_reaction

    The silicon plays the key role in stabilizing the carbocation of carbon at the β-position. Hosomi-Sakurai reaction is also applicable for other functional groups such as enones, where conjugate addition is usually seen. In figure 2, the Hosomi- Sakurai reaction has been shown using a cinnamoyl ketone.