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  2. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    The benzyl cation or phenylcarbenium ion is the carbocation with formula C 6 H 5 CH + 2; the benzyl anion or phenylmethanide ion is the carbanion with the formula C 6 H 5 CH − 2. None of these species can be formed in significant amounts in the solution phase under normal conditions, but they are useful referents for discussion of reaction ...

  3. Benzyl potassium - Wikipedia

    en.wikipedia.org/wiki/Benzyl_potassium

    Benzylpotassium is an organopotassium compound with the formula C 6 H 5 CH 2 K, an orange powder. Like organo-alkali metal reagents in general, benzyl potassium is highly reactive, so much so that it reacts with most solvents. It is highly air sensitive.

  4. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichloro-5,6-dicyano-1...

    2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (or DDQ) is the chemical reagent with formula C 6 Cl 2 (CN) 2 O 2. This oxidant is useful for the dehydrogenation of alcohols, [3] phenols, [4] and steroid ketones. [5] DDQ decomposes in water, but is stable in aqueous mineral acid. [6]

  5. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol (also known as α-cresol) is an aromatic alcohol with the formula C 6 H 5 CH 2 OH. The benzyl group is often abbreviated "Bn" (not to be confused with "Bz" which is used for benzoyl), thus benzyl alcohol is denoted as BnOH. Benzyl alcohol is a colorless liquid with a mild pleasant aromatic odor.

  6. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl chloride, or α-chlorotoluene, is an organic compound with the formula C 6 H 5 CH 2 Cl. This colorless liquid is a reactive organochlorine compound that is a widely used chemical building block .

  7. Benzal chloride - Wikipedia

    en.wikipedia.org/wiki/Benzal_chloride

    Benzal chloride is an organic compound with the formula C 6 H 5 CHCl 2. [1] This colourless liquid is a lachrymator and is used as a building block in organic synthesis . Preparation and usage

  8. List of benzo compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_benzo_compounds

    Letters and numbers in the parent compound Structural formula of the benzocompound Benzocompound Anthracene: Benzo[a]anthracene: by adding four extra carbon atoms to the parent compound, the leftmost upper ring is formed. Phenanthrene: Benzo[b]fenanthrene: by adding four carbon atoms to the parent compound the right most ring is formed. Clearly ...

  9. Dibenzyl ether - Wikipedia

    en.wikipedia.org/wiki/Dibenzyl_ether

    Dibenzylether is the organic compound with the formula (C 6 H 5 CH 2) 2 O. It is classified as an ether derived from benzyl alcohol. A colorless, nearly odorless oil, the compound's main use is as a plasticizer. It is prepared by treating benzyl chloride with base. [1]