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The Roman numerals in fact show the oxidation number, but in simple ionic compounds (i.e., not metal complexes) this will always equal the ionic charge on the metal. For a simple overview see [1] Archived 2008-10-16 at the Wayback Machine , for more details see selected pages from IUPAC rules for naming inorganic compounds Archived 2016-03-03 ...
This is a difference from organic compound naming and substitutive naming where chlorine is treated as neutral and it becomes chloro, as in PCl 3, which can be named as either substitutively or additively as trichlorophosphane or trichloridophosphorus respectively. Similarly if the anion names end in -ite, -ate then the ligand names are -ito, -ato.
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.
A mnemonic is a memory aid used to improve long-term memory and make the process of consolidation easier. Many chemistry aspects, rules, names of compounds, sequences of elements, their reactivity, etc., can be easily and efficiently memorized with the help of mnemonics.
Chrome Azurol S: 1667-99-8 C 23 H 19 ClF 3 NO 3: cyhalothrin: C 23 H 24 O 4 S Kadethrin: 58769-20-3 C 23 H 28 N 2 O Iferanserin: 58754-46-4 C 23 H 28 N 2 O 4: Pleiocarpine: C 23 H 38 N 2 OS Laucysteinamide A: 2255376-67-9 C 23 H 41 NO 2: Terminaline: 15112-49-9 C 24 H 17 F 6 NO 3: Tarocin A: C 24 H 29 FN 6: Ralimetinib: 862505-00-8 C 24 H 45 ...
The substituent name for a ring compound is cyclo. The indication (substituent name) for a six carbon chain is hex. The chemical ending for a single bonded carbon chain is ane. The chemical ending for an alcohol is ol. The two chemical endings are combined for an ending of anol indicating a single bonded carbon chain with an alcohol attached to it.
For groups of compounds named after a simple parent compound, articles about the group should be located at the plural of the parent compound name, e.g. hydrazines, silanes, boranes, diphosphenes. Similarly, salts and esters of carboxylic acids should collectively be referred to by the plural of the carboxylate.