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  2. Hydrophobic effect - Wikipedia

    en.wikipedia.org/wiki/Hydrophobic_effect

    The hydrophobic effect was found to be entropy-driven at room temperature because of the reduced mobility of water molecules in the solvation shell of the non-polar solute; however, the enthalpic component of transfer energy was found to be favorable, meaning it strengthened water-water hydrogen bonds in the solvation shell due to the reduced ...

  3. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Solvents can be broadly classified into two categories: polar and non-polar. A special case is elemental mercury, whose solutions are known as amalgams; also, other metal solutions exist which are liquid at room temperature. Generally, the dielectric constant of the solvent provides a rough measure of a solvent's polarity.

  4. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    This arises from the fact that polar solvents stabilize the formation of the carbocation intermediate to a greater extent than the non-polar-solvent conditions. This is apparent in the ΔE a, ΔΔG ‡ activation. On the right is an S N 2 reaction coordinate diagram. Note the decreased ΔG ‡ activation for the non-polar-solvent reaction ...

  5. Hydrophobe - Wikipedia

    en.wikipedia.org/wiki/Hydrophobe

    Examples of hydrophobic molecules include the alkanes, oils, fats, and greasy substances in general. Hydrophobic materials are used for oil removal from water, the management of oil spills, and chemical separation processes to remove non-polar substances from polar compounds. [2] Hydrophobic is often used interchangeably with lipophilic, "fat ...

  6. Glowmatography - Wikipedia

    en.wikipedia.org/wiki/Glowmatography

    Glow stick solutions and chalk sticks - preparation for experiment Glowmatography [ 1 ] is a laboratory technique for the separation of dyes present in solutions contained in glow sticks . The chemical components of such solutions can be chromatographically separated into polar and nonpolar components.

  7. Micelle - Wikipedia

    en.wikipedia.org/wiki/Micelle

    In a non-polar solvent, it is the exposure of the hydrophilic head groups to the surrounding solvent that is energetically unfavourable, giving rise to a water-in-oil system. In this case, the hydrophilic groups are sequestered in the micelle core and the hydrophobic groups extend away from the center.

  8. 1,1,1-Trichloroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,1-Trichloroethane

    1,1,1-Trichloroethane is an excellent solvent for many organic compounds and also one of the least toxic of the chlorinated hydrocarbons.It is generally considered non-polar, but owing to the good polarizability of the chlorine atoms, it is a superior solvent for organic compounds that do not dissolve well in hydrocarbons such as hexane.

  9. Separatory funnel - Wikipedia

    en.wikipedia.org/wiki/Separatory_funnel

    The separating funnel relies on the concept of "like dissolves like", which describes the ability of polar solvents to dissolve polar solutes and non-polar solvents to dissolve non-polar solutes. When the separating funnel is agitated, each solute migrates to the solvent (also referred to as "phase") in which it is more soluble.

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