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Cyclopentane can be fluorinated to give compounds ranging from C 5 H 9 F to perfluorocyclopentane C 5 F 10. Such species are conceivable refrigerants and specialty solvents. [15] [16] The cyclopentane ring is pervasive in natural products including many useful drugs. Examples include most steroids, prostaglandins, and some lipids.
If the acyl groups are different, then they are named in alphabetical order in the same way, with anhydride replacing acid and IUPAC name consists of three words. For example, CH 3 CO−O−OCCH 3 is called ethanoic anhydride and CH 3 CO−O−OCCH 2 CH 3 is called ethanoic propanoic anhydride.
An example of a common name is terpineol, the name of which can tell us only that it is an alcohol (because the suffix "-ol" is in the name) and it should then have a hydroxyl group (–OH) attached to it. The IUPAC naming system for organic compounds can be demonstrated using the example provided in the adjacent image.
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
For example, R-22 has one carbon atom, one hydrogen atom (2−1 = 1), two fluorine atoms, and one chlorine atom (4−2−1 = 1), so it is chlorodifluoromethane, while R-134 has two carbon atoms (2−1 = 1), two hydrogen atoms (3−1 = 2), four fluorine atoms, and no chlorine atoms (6−2−4 = 0), so it is one of the tetrafluoroethanes. This ...
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.
Names Preferred IUPAC name. Cyclobutane. Other names ... Cyclopropane; Cyclopentane: Except where otherwise noted, ... One example is pentacycloanammoxic acid, [3] ...
Examples are borazine (B 3 N 3 ring), hexachlorophosphazenes (P 3 N 3 rings), and tetrasulfur tetranitride S 4 N 4. In comparison with organic heterocycles, which have numerous commercial applications, inorganic ring systems are mainly of theoretical interest. IUPAC recommends the Hantzsch-Widman nomenclature for naming heterocyclic compounds. [5]