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  2. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    Linear alkylbenzenes (sometimes also known as LABs) are a family of organic compounds with the formula C 6 H 5 C n H 2n+1. Typically, n lies between 10 and 16, although generally supplied as a tighter cut, such as C 12 -C 15 , C 12 -C 13 and C 10 -C 13 , for detergent use. [ 1 ]

  3. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    It is the raw material in the production of synthetic sulfonate detergents, which are found in a variety of household products such as soap, shampoo, toothpaste, laundry detergent, etc. Linear alkylbenzenes (LAB) and branched alkylbenzenes (BAB) are families of alkylbenzene used to prepare synthetic sulfonates. However, LABs are more ...

  4. Kipp's apparatus - Wikipedia

    en.wikipedia.org/wiki/Kipp's_apparatus

    Kipp's apparatus, also called a Kipp generator, is an apparatus designed for preparation of small volumes of gases. It was invented around 1844 by the Dutch pharmacist Petrus Jacobus Kipp and widely used in chemical laboratories and for demonstrations in schools into the second half of the 20th century.

  5. Benzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzene_(data_page)

    *** Benzene is a carcinogen (cancer-causing agent). *** Very flammable. The pure material, and any solutions containing it, constitute a fire risk. Safe handling: Benzene should NOT be used at all unless no safer alternatives are available. If benzene must be used in an experiment, it should be handled at all stages in a fume cupboard.

  6. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    Formyl functional group is shown in blue. Formylation refers to any chemical processes in which a compound is functionalized with a formyl group (-CH=O). In organic chemistry, the term is most commonly used with regards to aromatic compounds (for example the conversion of benzene to benzaldehyde in the Gattermann–Koch reaction).

  7. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    Aromatization is a chemical reaction in which an aromatic system is formed from a single nonaromatic precursor. Typically aromatization is achieved by dehydrogenation of existing cyclic compounds, illustrated by the conversion of cyclohexane into benzene.

  8. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    In the laboratory it can be prepared by the dehydration of benzamide or benzaldehyde oxime [2] or by the Rosenmund–von Braun reaction using cuprous cyanide or NaCN/DMSO and bromobenzene. Hydrogenation of benzonitrile in principle gives benzylamine , but owing to transamination, dibenzylamine and tribenzylamine are also produced.

  9. Blanc chloromethylation - Wikipedia

    en.wikipedia.org/wiki/Blanc_chloromethylation

    The Blanc chloromethylation (also called the Blanc reaction) is the chemical reaction of aromatic rings with formaldehyde and hydrogen chloride to form chloromethyl arenes. . The reaction is catalyzed by Lewis acids such as zinc chlorid