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  2. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    In commercial applications, the alkylating agents are generally alkenes, some of the largest scale reactions practiced in industry.Such alkylations are of major industrial importance, e.g. for the production of ethylbenzene, the precursor to polystyrene, from benzene and ethylene and for the production of cumene from benzene and propene in cumene process:

  3. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol is used effectively for treating lice infestations as the active ingredient in lotion shampoo with 5% benzyl alcohol. [13] Benzyl alcohol is an ingredient used in the manufacture of soaps, topical creams, skin lotions, shampoos, and facial cleansers and is popular due to its anti-bacterial and anti-fungal properties.

  4. Phase-transfer catalyst - Wikipedia

    en.wikipedia.org/wiki/Phase-transfer_catalyst

    In chemistry, a phase-transfer catalyst or PTC is a catalyst that facilitates the transition of a reactant from one phase into another phase where reaction occurs. Phase-transfer catalysis is a special form of catalysis and can act through homogeneous catalysis or heterogeneous catalysis methods depending on the catalyst used.

  5. Transalkylation - Wikipedia

    en.wikipedia.org/wiki/Transalkylation

    Transalkylation reactions of six to ten carbon methylated aromatics are often performed with the cofeed of hydrogen gas, over a zeolite based solid catalyst. Industrial processes operate the transalkylation reactor at elevated temperature and pressure to achieve desired process economics.

  6. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It is a colourless liquid with a pleasant floral odor.

  7. Carbonyl reduction - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_reduction

    In organic chemistry, carbonyl reduction is the conversion of any carbonyl group, usually to an alcohol. It is a common transformation that is practiced in many ways. [ 1 ] Ketones , aldehydes , carboxylic acids , esters , amides , and acid halides - some of the most pervasive functional groups , -comprise carbonyl compounds.

  8. Photolabile protecting group - Wikipedia

    en.wikipedia.org/wiki/Photolabile_protecting_group

    Figure 5: Benzyl-based PPGs with polycyclic aromatic cores: A) benzene; B) naphthalene; C) anthracene; D) phenanthrene; E) phyene and; F) perylene. Barltrop and Schofield first demonstrated the use of a benzyl-based PPG, [ 4 ] structural variations have focused on substitution to the benzene ring, as well as extension of the aromatic core.

  9. Benzilic acid rearrangement - Wikipedia

    en.wikipedia.org/wiki/Benzilic_acid_rearrangement

    The carboxylic acid in intermediate 4 is less basic than the alkoxide and therefore reversible proton transfer takes place favoring intermediate 5 which is protonated on acidic workup to the final α-hydroxy–carboxylic acid 6. Calculations show that an accurate description of the reaction sequence is possible with the participation of 4 water ...