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  2. 2,3-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichlorophenol

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  3. Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenol

    3,4-Dichlorophenol 3,5-Dichlorophenol Dichlorophenols are used as intermediates in the manufacture of more complex chemical compounds, including the common herbicide 2,4-dichlorophenoxyacetic acid (2,4-D).

  4. Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Trichlorophenol

    2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position. There are six different isomers: 2,3,4-Trichlorophenol

  5. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC nomenclature is used for the naming of chemical compounds, based on their chemical composition and their structure. [1] For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain.

  6. 3,4-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/3,4-Dichlorophenol

    Download as PDF; Printable version; In other projects ... 3,4-Dichlorophenol Names Preferred IUPAC name. 3,4-Dichlorophenol ... with the molecular formula Cl 2 C 6 H ...

  7. 2,6-Dichlorophenol - Wikipedia

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

    2,6-Dichlorophenol is a compound with formula C 6 H 3 Cl 2 OH. It is one of the six isomers of dichlorophenol. It is a colorless solid. Its pK a is 6.78, which is about 100x more acidic than 2-chlorophenol (8.52) and 1000x more acidic than phenol itself (9.95). [3]

  8. 2,5-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,5-dichlorophenol

    Download as PDF; Printable version; In other projects ... 2,5-Dichlorophenol Names Preferred IUPAC name. 2,5-Dichlorophenol ... is a chlorinated derivative of phenol ...

  9. Polyphenol - Wikipedia

    en.wikipedia.org/wiki/Polyphenol

    The name derives from the Ancient Greek word πολύς (polus, meaning "many, much") and the word ‘phenol’ which refers to a chemical structure formed by attachment of an aromatic benzenoid ring to a hydroxyl (-OH) group (hence the -ol suffix). The term "polyphenol" has been in use at least since 1894.