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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.
Many other names for sets of elements are in common use; others have been used throughout history. These sets usually do not aim to cover the whole periodic table (as for example period does), and often overlap or have boundaries that differ between authors. Some examples: Metals and nonmetals
The main purpose of chemical nomenclature is to disambiguate the spoken or written names of chemical compounds: each name should refer to one compound. Secondarily, each compound should have only one name, although in some cases some alternative names are accepted. Preferably, the name should also represent the structure or chemistry of a compound.
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.
Like the periodic table, the list below organizes the elements by the number of protons in their atoms; it can also be organized by other properties, such as atomic weight, density, and electronegativity. For more detailed information about the origins of element names, see List of chemical element name etymologies.
The formal list is used. The name of the most electronegative element is modified to end in -ide and the more electropositive elements name is left unchanged. Taking the binary compound of sodium and chlorine: chlorine is found first in the list so therefore comes last in the name. Other examples are PCl 5 phosphorus pentachloride
Although most compounds are referred to by their IUPAC systematic names (following IUPAC nomenclature), traditional names have also been kept where they are in wide use or of significant historical interests.
The main carbon chain is the longest possible continuous chain. The chemical affix denotes what type of molecule it is. For example, the ending ane denotes a single bonded carbon chain, as in "hexane" (C 6 H 14). [30] Another example of IUPAC organic nomenclature is cyclohexanol: Cyclohexanol. The substituent name for a ring compound is cyclo.