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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
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). [ 1 ]
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 ...
Download as PDF; Printable version; In other projects ... 2,5-Dichlorophenol Names Preferred IUPAC name. 2,5-Dichlorophenol ... is a chlorinated derivative of phenol ...
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)
2,3-Dichloroaniline is an organic compound with the formula C 6 H 3 Cl 2 (NH 2). It is one of several isomers of dichloroaniline . It is a colorless oil although commercial samples often appear colored.
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]