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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. Polydimethylsiloxane - Wikipedia

    en.wikipedia.org/wiki/Polydimethylsiloxane

    It is one of several types of silicone oil (polymerized siloxane). The applications of PDMS range from contact lenses and medical devices to elastomers ; it is also present in shampoos (as it makes hair shiny and slippery ), food ( antifoaming agent ), caulk , lubricants and heat-resistant tiles .

  5. Silicone oil - Wikipedia

    en.wikipedia.org/wiki/Silicone_oil

    Silicone oil serves as an effective gun lubricant, suitable for use with the rubber, plastic, and metal components commonly found in firearms. Its high surface adhesion allows it to create a long-lasting protective film, which is beneficial for preserving guns during prolonged storage.

  6. 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.

  7. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    The group must have one of two things: a lone pair of electrons, or a negative charge. In the +M effect, the pi electrons are transferred from the group towards the conjugate system, increasing the density of the system. Due to the increase in electron density, the conjugate system will develop a more negative charge.

  8. Brain study shows Conrad Dobler, once regarded as NFL's ... - AOL

    www.aol.com/brain-study-shows-conrad-dobler...

    The family of Conrad Dobler, once regarded as the dirtiest player in the NFL, said he had CTE based on a study of his brain after his death in 2023.

  9. Deprotonation - Wikipedia

    en.wikipedia.org/wiki/Deprotonation

    The pK a of a compound is determined by many aspects, but the most significant is the stability of the conjugate base. This is primarily determined by the ability (or inability) of the conjugated base to stabilize negative charge. One of the most important ways of assessing a conjugate base's ability to distribute negative charge is using ...