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In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1] [2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]
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 key article setting out the CIP sequence rules was published in 1966, [5] and was followed by further refinements, [6] before it was incorporated into the rules of the International Union of Pure and Applied Chemistry (IUPAC), the official body that defines organic nomenclature, in 1974.
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 ...
The 2005 IUPAC Red Book excludes hydrogen from the main-group elements, but this exclusion is often not followed in practice, and the 2011 IUPAC Principles of Chemical Nomenclature does not exclude hydrogen. The codification of those names is in the 2005 Red Book, when elements past Rg had not yet been approved.
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 ...
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 ...
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.