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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
Chemical structure of 2,4-dichlorophenol. Dichlorophenols (DCPs) are any of several chemical compounds which are derivatives of phenol containing two chlorine atoms. There are six isomers:
The main structure of chemical names according to IUPAC nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry (Red Book) IUPAC nomenclature of organic chemistry (Blue Book)
CH 3 (CH 2) n C(=O)N(CH 2 CH 2 OH) 2, where n is from 8 to 18 foaming and/or emulsifying agent cyclohexasiloxane: Dodecamethylcyclohexasiloxane (D6) solvent cyclopentasiloxane (a type of silicone) [citation needed] Decamethylcyclopentasiloxane (D5) solvent cetyl alcohol: CH 3 (CH 2) 15 OH various calcium sodium borosilicate: glass (flakes ...
English. Read; Edit; View history ... 2,5-Dichlorophenol Names Preferred IUPAC name ... is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 ...
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]
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.