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  2. Beryllium bromide - Wikipedia

    en.wikipedia.org/wiki/Beryllium_bromide

    It can be prepared by reacting beryllium metal with elemental bromine at temperatures of 500 °C to 700 °C: [1]. Be + Br 2 → BeBr 2. When the oxidation is conducted on an ether suspension, one obtains colorless dietherate: [4]

  3. 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

  4. Beryllium hydride - Wikipedia

    en.wikipedia.org/wiki/Beryllium_hydride

    Beryllium hydride (systematically named poly[beryllane(2)] and beryllium dihydride) is an inorganic compound with the chemical formula (BeH 2) n (also written ([BeH 2]) n or BeH 2).

  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. Barium bromide - Wikipedia

    en.wikipedia.org/wiki/Barium_bromide

    Barium bromide is a precursor to chemicals used in photography and to other bromides. Historically, barium bromide was used to purify radium in a process of fractional crystallization devised by Marie Curie.

  7. Beryllium chloride - Wikipedia

    en.wikipedia.org/wiki/Beryllium_chloride

    It is a colourless, hygroscopic solid that dissolves well in many polar solvents. Its properties are similar to those of aluminium chloride , due to beryllium 's diagonal relationship with aluminium .

  8. 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 ...

  9. Hydrophobe - Wikipedia

    en.wikipedia.org/wiki/Hydrophobe

    Hydrophobic molecules tend to be nonpolar and, thus, prefer other neutral molecules and nonpolar solvents. Because water molecules are polar, hydrophobes do not dissolve well among them. Hydrophobic molecules in water often cluster together, forming micelles. Water on hydrophobic surfaces will exhibit a high contact angle.