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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 ]
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.
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 formula Na 2 SO 3 denotes that the cation is sodium, or Na +, and that the anion is the sulfite ion (SO 2− 3). Therefore, this compound is named sodium sulfite. If the given formula is Ca(OH) 2, it can be seen that OH − is the hydroxide ion. Since the charge on the calcium ion is 2+, it makes sense there must be two OH − ions
If it applies but no heteroatom is found in a chain, it is preferred over multiplicative nomenclature. Example: 3-phospha-2,5,7-trisilaoctane refers to CH 3-SiH 2-PH-CH 2-SiH 2-CH 2-SiH 2-CH 3. Skeletal replacement mainly replaces carbon with other atoms, or in the case of phane nomenclature, whole "superatom" rings.
The names "caffeine" and "3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione" both signify the same chemical compound.The systematic name encodes the structure and composition of the caffeine molecule in some detail, and provides an unambiguous reference to this compound, whereas the name "caffeine" simply names it.
substitutive naming based on parent hydrides (GeCl 2 Me 2 dichlorodimethylgermane) additive naming ([MnFO 3] fluoridotrioxidomanganese) Additionally there are recommendations for the following: naming of cluster compounds; allowed names for inorganic acids and derivatives; naming of solid phases e.g. non-stoichiometric phases
A full edition was published in 1979, [1] an abridged and updated version of which was published in 1993 as A Guide to IUPAC Nomenclature of Organic Compounds. [2] Both of these are now out-of-print in their paper versions, but are available free of charge in electronic versions.