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  2. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    Similar to other phenols, the hydroxyl groups on the aromatic ring of a benzenediol are weakly acidic. Each benzenediol can lose an H + from one of the hydroxyls to form a type of phenolate ion. The Dakin oxidation is an organic redox reaction in which an ortho - or para -hydroxylated phenyl aldehyde ( −CH=O ) or ketone ( >C=O ) reacts with ...

  3. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    Ortho effect is an organic chemistry phenomenon where the presence of a chemical group at the at ortho position or the 1 and 2 position of a phenyl ring, relative to the carboxylic compound changes the chemical properties of the compound.

  4. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    Catechol (/ ˈ k æ t ɪ tʃ ɒ l / or / ˈ k æ t ɪ k ɒ l /), also known as pyrocatechol or 1,2-dihydroxybenzene, is an organic compound with the molecular formula C 6 H 4 (OH) 2. It is the ortho isomer of the three isomeric benzenediols .

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The simplest alkene, ethylene (C 2 H 4) (or "ethene" in the IUPAC nomenclature) is the organic compound produced on the largest scale industrially. [5] Aromatic compounds are often drawn as cyclic alkenes, however their structure and properties are sufficiently distinct that they are not classified as alkenes or olefins. [3]

  6. Hydroxylation - Wikipedia

    en.wikipedia.org/wiki/Hydroxylation

    2R 3 C−H + O 22 R 3 C−OH R 3 C−H + O 2 + 2e − + 2H + → R 3 C−OH + H 2 O. Since O 2 itself is a slow and unselective hydroxylating agent, catalysts are required to accelerate the pace of the process and to introduce selectivity. [1] Hydroxylation is often the first step in the degradation of organic compounds in air.

  7. C2-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C2-Benzenes

    The C 2 benzenes are a class of organic aromatic compounds which contain a benzene ring and two other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers. There are three xylenes and one ethylbenzene .

  8. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...

  9. Hydroxy group - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_group

    The hydroxy group is pervasive in chemistry and biochemistry. Many inorganic compounds contain hydroxyl groups, including sulfuric acid, the chemical compound produced on the largest scale industrially. [2] Hydroxy groups participate in the dehydration reactions that link simple biological molecules into long chains.