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  2. Dibenzyl ether - Wikipedia

    en.wikipedia.org/wiki/Dibenzyl_ether

    Dibenzyl ether Names Preferred IUPAC name. ... Melting point: 3.6 °C (38.5 °F; 276.8 K) Boiling point: 298 °C (568 °F; 571 K) Hazards

  3. 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.

  4. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

  5. Melting point - Wikipedia

    en.wikipedia.org/wiki/Melting_point

    The melting point (or, rarely, liquefaction point) of a substance is the temperature at which it changes state from solid to liquid. At the melting point the solid and liquid phase exist in equilibrium. The melting point of a substance depends on pressure and is usually specified at a standard pressure such as 1 atmosphere or 100 kPa.

  6. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    A typical example of the first group is the solvent and anaesthetic diethyl ether, commonly referred to simply as "ether" (CH 3 −CH 2 −O−CH 2 −CH 3). Ethers are common in organic chemistry and even more prevalent in biochemistry , as they are common linkages in carbohydrates and lignin .

  7. Diphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_ether

    Diphenyl ether is the organic compound with the formula (C 6 H 5) 2 O. It is a colorless, low-melting solid. It is a colorless, low-melting solid. This, the simplest diaryl ether , has a variety of niche applications.

  8. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl ethers are often derived from benzyl chloride. Benzyl chloride reacts with aqueous sodium hydroxide to give dibenzyl ether. In organic synthesis, benzyl chloride is used to introduce the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester.

  9. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    For example, occupational exposure to organic solvents has been associated with higher numbers of painters suffering from alcoholism. [35] Ethanol has a synergistic effect when taken in combination with many solvents; for instance, a combination of toluene / benzene and ethanol causes greater nausea / vomiting than either substance alone.