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  2. 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.

  3. Alkylated naphthalene - Wikipedia

    en.wikipedia.org/wiki/Alkylated_naphthalene

    Alkylated naphthalenes are chemical compounds made by the alkylation of naphthalene or its derivatives with an olefin. These compounds are used as synthetic base oils , and are claimed to have improved oxidative stability over some conventional base oils.

  4. Alkylation - Wikipedia

    en.wikipedia.org/wiki/Alkylation

    Alkylation is a chemical reaction that entails transfer of an alkyl group. The alkyl group may be transferred as an alkyl carbocation, a free radical, a carbanion, or a carbene (or their equivalents). [1] Alkylating agents are reagents for effecting alkylation. Alkyl groups can also be removed in a process known as dealkylation.

  5. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    Friedel–Crafts alkylations can be reversible. Although this is usually undesirable it can be exploited; for instance by facilitating transalkylation reactions. [10] 1,3-Diisopropylbenzene is produced via transalkylation, a special form of Friedel–Crafts alkylation. It also allows alkyl chains to be added reversibly as protecting groups.

  6. 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]

  7. Naphthalenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Naphthalenesulfonate

    Naphthalenesulfonates are derivatives of sulfonic acid which contain a naphthalene functional unit. A related family of compounds are the aminonaphthalenesulfonic acids.Of commercial importance are the alkylnaphthalene sulfonates, which are used as superplasticizers in concrete.

  8. Weight loss may be helped by drinking this, study suggests - AOL

    www.aol.com/drinking-sparkling-water-could...

    Weight loss can occur when people engage in increased physical activity, decrease their caloric intake and eat a healthier selection of foods, which includes minimizing ultraprocessed, fried and ...

  9. 2,6-Dimethylnaphthalene - Wikipedia

    en.wikipedia.org/wiki/2,6-Dimethylnaphthalene

    2,6-Dimethylnaphthalene is mainly used for the preparation of 2,6-naphthalenedicarboxylic acid by oxidation of 2,6-dimethylnaphthalene in the liquid phase. 2,6-Naphthalenedicarboxylic acid is a monomer for the production of high-performance polymers, in particular poly (ethylene-2,6-naphthalene dicarboxylate) or shorter polyethylene naphthalate (PEN). [4]