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  2. File:Organic chemistry for advanced students (IA ...

    en.wikipedia.org/wiki/File:Organic_chemistry_for...

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  3. Work-up - Wikipedia

    en.wikipedia.org/wiki/Work-up

    The product is isolated from the mixture by the following work-up: [3] Synthesis of 4-methylcyclohexene with work-up step in red. A concentrated solution of sodium chloride in water, known as a brine solution, is added to the mixture and the layers are allowed to separate. The brine is used to remove any acid or water from the organic layer.

  4. File:Practical work in organic chemistry (IA ...

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  5. File:Organic chemistry for advanced students (IA ...

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  6. One-pot synthesis - Wikipedia

    en.wikipedia.org/wiki/One-pot_synthesis

    In chemistry a one-pot synthesis is a strategy to improve the efficiency of a chemical reaction in which a reactant is subjected to successive chemical reactions in just one reactor. This is much desired by chemists because avoiding a lengthy separation process and purification of the intermediate chemical compounds can save time and resources ...

  7. File:Organic Chemistry.pdf - Wikipedia

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  8. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Organic synthesis is an important chemical process that is integral to many scientific fields. Examples of fields beyond chemistry that require organic synthesis include the medical industry, pharmaceutical industry, and many more. Organic processes allow for the industrial-scale creation of pharmaceutical products.

  9. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).