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  2. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    [1] [3] Dehydrogenation also converts saturated fats to unsaturated fats. One of the largest scale dehydrogenation reactions is the production of styrene by dehydrogenation of ethylbenzene. Typical dehydrogenation catalysts are based on iron(III) oxide, promoted by several percent potassium oxide or potassium carbonate. [4] C 6 H 5 CH 2 CH 3 ...

  3. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The conversion of ethanol to ethylene is a fundamental example: [3] [4] CH 3 CH 2 OH → H 2 C=CH 2 + H 2 O. The reaction is accelerated by acid catalysts such as sulfuric acid and certain zeolites. These reactions often proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. [5] Some alcohols are prone to dehydration.

  4. Anhydrous - Wikipedia

    en.wikipedia.org/wiki/Anhydrous

    Anhydrous solvents are commercially available from chemical suppliers, and are packaged in sealed containers to maintain dryness. [4] Typically anhydrous solvents will contain approximately 10 ppm of water and will increase in wetness if they are not properly stored. Organic solutions can be dried using a range of drying agents.

  5. Dry distillation - Wikipedia

    en.wikipedia.org/wiki/Dry_distillation

    Dry distillation is the heating of solid materials to produce gaseous products (which may condense into liquids or solids). The method may involve pyrolysis or thermolysis, or it may not (for instance, a simple mixture of ice and glass could be separated without breaking any chemical bonds, but organic matter contains a greater diversity of molecules, some of which are likely to break).

  6. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    Dimethylacetamide is commonly used as a solvent for fibers (e.g., polyacrylonitrile, spandex) or in the adhesive industry. [5] It is also employed in the production of pharmaceuticals and plasticizers as a reaction medium. A solution of lithium chloride in DMAc (LiCl/DMAc) can dissolve cellulose. Unlike many other cellulose solvents, LiCl/DMAc ...

  7. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols.

  8. Acid–base extraction - Wikipedia

    en.wikipedia.org/wiki/Acid–base_extraction

    Acid–base extraction is a subclass of liquid–liquid extractions and involves the separation of chemical species from other acidic or basic compounds. [1] It is typically performed during the work-up step following a chemical synthesis to purify crude compounds [2] and results in the product being largely free of acidic or basic impurities.

  9. p-Toluenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluenesulfonic_acid

    p-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH 3 C 6 H 4 SO 3 H. It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6] The CH 3 C 6 H 4 SO 2 group is known as the tosyl group and is often abbreviated as