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  2. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula C H 2 Cl 2. This colorless, volatile liquid with a chloroform-like, sweet odor is widely used as a solvent. Although it is not miscible with water, it is slightly polar, and miscible with many organic solvents. [12]

  3. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Strongly polar compounds like sugars (e.g. sucrose) or ionic compounds, like inorganic salts (e.g. table salt) dissolve only in very polar solvents like water, while strongly non-polar compounds like oils or waxes dissolve only in very non-polar organic solvents like hexane.

  4. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    When comparing a polar and nonpolar molecule with similar molar masses, the polar molecule in general has a higher boiling point, because the dipole–dipole interaction between polar molecules results in stronger intermolecular attractions. One common form of polar interaction is the hydrogen bond, which is also

  5. Polar aprotic solvent - Wikipedia

    en.wikipedia.org/wiki/Polar_aprotic_solvent

    A polar aprotic solvent is a solvent that lacks an acidic proton and is polar. Such solvents lack hydroxyl and amine groups. In contrast to protic solvents, these solvents do not serve as proton donors in hydrogen bonding, although they can be proton acceptors. Many solvents, including chlorocarbons and hydrocarbons, are classifiable as aprotic ...

  6. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  7. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    The most important is dichloromethane, which is mainly used as a solvent. Chloromethane is a precursor to chlorosilanes and silicones. Historically significant (as an anaesthetic), but smaller in scale is chloroform, mainly a precursor to chlorodifluoromethane (CHClF 2) and tetrafluoroethene which is used in the manufacture of Teflon. [2]

  8. Non-coordinating anion - Wikipedia

    en.wikipedia.org/wiki/Non-coordinating_anion

    Another advantage of these anions is that their salts are more soluble in non-polar organic solvents such as dichloromethane, toluene, and, in some cases, even alkanes. [citation needed] Polar solvents, such as acetonitrile, THF, and water, tend to bind to electrophilic centers, in which cases, the use of a non-coordinating anion is pointless.

  9. Multiphasic liquid - Wikipedia

    en.wikipedia.org/wiki/Multiphasic_liquid

    Nonpolar solvent A / solvent B / polymer soluble in solvent B and water / salt / water e.g. 10.9% heptane, 15.5% dichloromethane, 7.1% polyethylene oxide, 66.5% sodium sulfate (> 0.1%) in water; Nonpolar solvent / Polar solvent / salt / water / Fluorinated solvent e.g. Hexane, isopropanol, brine, perfluoromethylcyclohexane