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The Geneva Nomenclature of 1892 was created as a result of many other meetings in the past, the first of which was established in 1860 by August Kekulé. Another entity called the International Association of Chemical Societies (IACS) existed, and on 1911, gave vital propositions the new one should address: [ 2 ]
The Americans also wished to name element 106 seaborgium. This naming dispute ran from the 1970s (when the elements were discovered) to the 1990s, when the International Union of Pure and Applied Chemistry (IUPAC) created a tentative list of the element names for elements 104 to 109. The Americans, however, refused to agree with these names ...
Chemical nomenclature however (with IUPAC nomenclature as the best example) is necessarily more restrictive: Its purpose is to standardize communication and practice so that, when a chemical term is used it has a fixed meaning relating to chemical structure, thereby giving insights into chemical properties and derived molecular functions. These ...
To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...
A chemical element, often simply called an element, is a type of atom which has a specific number of protons in its atomic nucleus (i.e., a specific atomic number, or Z). [ 1 ] The definitive visualisation of all 118 elements is the periodic table of the elements , whose history along the principles of the periodic law was one of the founding ...
Superactinides – Hypothetical series of elements 121 to 157, which includes a predicted "g-block" of the periodic table. Transactinide elements – Elements after the actinides (atomic number greater than 103). Transplutonium elements – Elements with atomic number greater than 94. Transuranium elements – Elements with atomic number ...
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E–Z configuration, or the E–Z convention, is the IUPAC preferred method of describing the absolute stereochemistry of double bonds in organic chemistry.It is an extension of cis–trans isomer notation (which only describes relative stereochemistry) that can be used to describe double bonds having two, three or four substituents.