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  2. Recrystallization (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Recrystallization_(chemistry)

    The solution is then cooled to further induce recrystallization. [6] A solvent is added (white) to a compound (light orange) → Compound is heated to dissolution, providing a saturated solution (light orange) → Second solvent (orange) added to the saturated solution (light orange) to give a mixed solvent system (orange) → Mixed solvent ...

  3. List of purification methods in chemistry - Wikipedia

    en.wikipedia.org/wiki/List_of_purification...

    Recrystallization: In analytical and synthetic chemistry work, purchased reagents of doubtful purity may be recrystallised, e.g. dissolved in a very pure solvent, and then crystallized, and the crystals recovered, in order to improve and/or verify their purity.

  4. Sodium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Sodium_naphthalene

    Sodium naphthalene is an organic salt with the chemical formula Na + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na +. [1]

  5. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    A naphthalene molecule can be viewed as the fusion of a pair of benzene rings. (In organic chemistry, rings are fused if they share two or more atoms.) As such, naphthalene is classified as a benzenoid polycyclic aromatic hydrocarbon (PAH). [19] The eight carbon atoms that are not shared by the two rings carry one hydrogen atom each.

  6. Fractional crystallization (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Fractional_crystallization...

    In chemistry, fractional crystallization is a stage-wise separation technique that relies on the liquid–solid phase change. This technique fractionates via differences in crystallization temperature and enables the purification of multi-component mixtures, as long as none of the constituents can act as solvents to the others.

  7. Thermal rearrangement of aromatic hydrocarbons - Wikipedia

    en.wikipedia.org/wiki/Thermal_rearrangement_of...

    The first proposed mechanism for a thermal rearrangement of an aromatic compound was for the automerization of naphthalene. It was suggested that the rearrangement of naphthalene occurred due to reversibility of the isomerization of azulene to naphthalene. [2] [3] This mechanism would therefore involve an azulene intermediate and is depicted below:

  8. Supersaturation - Wikipedia

    en.wikipedia.org/wiki/Supersaturation

    Carbohydrates are a class of such compounds; The thermodynamic barrier to formation of crystals is rather high because of extensive and irregular hydrogen bonding with the solvent, water. For example, although sucrose can be recrystallised easily, its hydrolysis product, known as " invert sugar " or "golden syrup" is a mixture of glucose and ...

  9. Enthalpy change of solution - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_change_of_solution

    The equilibrium, between the gas as a separate phase and the gas in solution, will by Le Châtelier's principle shift to favour the gas going into solution as the temperature is decreased (decreasing the temperature increases the solubility of a gas). When a saturated solution of a gas is heated, gas comes out of the solution.