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IUPAC

A Wisdom Archive on IUPAC

IUPAC

A selection of articles related to IUPAC

We recommend this article: IUPAC - 1, and also this: IUPAC - 2.
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iupac, International Union of Pure and Applied Chemistry, IUPAC nomenclature, Chemical element, Element naming controversy, Periodic table group, International Chemical Identifier (InChI)

ARTICLES RELATED TO IUPAC

IUPAC: Encyclopedia II - IUPAC nomenclature - Types of nomenclature

IUPAC nomenclature - Compositional nomenclature. IUPAC nomenclature - Substitutive nomenclature. IUPAC nomenclature - Additive nomenclature. ...

See also:

IUPAC nomenclature, IUPAC nomenclature - Aims of chemical nomenclature, IUPAC nomenclature - History, IUPAC nomenclature - Types of nomenclature, IUPAC nomenclature - Compositional nomenclature, IUPAC nomenclature - Substitutive nomenclature, IUPAC nomenclature - Additive nomenclature

Read more here: » IUPAC nomenclature: Encyclopedia II - IUPAC nomenclature - Types of nomenclature

IUPAC: Encyclopedia II - IUPAC nomenclature - History
The nomenclature of alchemy is rich in description, but does not effectively meet the aims outlined above. Opinions differ as to whether this was deliberate on the part of the practitioners of alchemy or whether it was a consequence of the particular (and often esoteric) theoretical framework in which they worked. While both explanations are probably valid to some extent, it is remarkable that the first "modern" system of chemical nomenclature appeared at the same time as the distinction (by Lavoisier) between elements ...

See also:

IUPAC nomenclature, IUPAC nomenclature - Aims of chemical nomenclature, IUPAC nomenclature - History, IUPAC nomenclature - Types of nomenclature, IUPAC nomenclature - Compositional nomenclature, IUPAC nomenclature - Substitutive nomenclature, IUPAC nomenclature - Additive nomenclature

Read more here: » IUPAC nomenclature: Encyclopedia II - IUPAC nomenclature - History

IUPAC: Encyclopedia II - IUPAC nomenclature - Aims of chemical nomenclature

The primary function of chemical nomenclature is to ensure that the person who hears or reads a chemical name is under no ambiguity as to which chemical compound it refers: each name should refer to a single substance. It is considered less important to ensure that each substance should have a single name, although the number of acceptable names is limited. It is also preferable that the name convey some information about the structure or chemistry of a compound. CAS numbers form an extreme example of names which do not perform this f ...

See also:

IUPAC nomenclature, IUPAC nomenclature - Aims of chemical nomenclature, IUPAC nomenclature - History, IUPAC nomenclature - Types of nomenclature, IUPAC nomenclature - Compositional nomenclature, IUPAC nomenclature - Substitutive nomenclature, IUPAC nomenclature - Additive nomenclature

Read more here: » IUPAC nomenclature: Encyclopedia II - IUPAC nomenclature - Aims of chemical nomenclature

IUPAC: Encyclopedia II - IUPAC nomenclature of organic chemistry - Ions

The IUPAC nomenclature also provides rules for naming ions. IUPAC nomenclature of organic chemistry - Hydron. Hydron is a generic term for hydrogen cation; protons, deuterons and tritons are all hydrons. IUPAC nomenclature of organic chemistry - Parent hydride cations. Simple cations formed by adding a hydron to a hydride of a halogen, chalcogen or nitrogen-family element are named by adding the suffix "-onium" to the element's root: H4N+ is ammoniu ...

See also:

IUPAC nomenclature of organic chemistry, IUPAC nomenclature of organic chemistry - Alkanes, IUPAC nomenclature of organic chemistry - Alkenes and Alkynes, IUPAC nomenclature of organic chemistry - Alcohols, IUPAC nomenclature of organic chemistry - Halogenated compounds, IUPAC nomenclature of organic chemistry - Ketones, IUPAC nomenclature of organic chemistry - Aldehydes, IUPAC nomenclature of organic chemistry - Carboxylic acids, IUPAC nomenclature of organic chemistry - Ethers, IUPAC nomenclature of organic chemistry - Esters, IUPAC nomenclature of organic chemistry - Amines and Amides, IUPAC nomenclature of organic chemistry - Cyclic compounds, IUPAC nomenclature of organic chemistry - Order of precedence of groups, IUPAC nomenclature of organic chemistry - Common nomenclature, IUPAC nomenclature of organic chemistry - Ketones, IUPAC nomenclature of organic chemistry - Aldehydes, IUPAC nomenclature of organic chemistry - Ions, IUPAC nomenclature of organic chemistry - Hydron, IUPAC nomenclature of organic chemistry - Parent hydride cations, IUPAC nomenclature of organic chemistry - Cations and substitution

Read more here: » IUPAC nomenclature of organic chemistry: Encyclopedia II - IUPAC nomenclature of organic chemistry - Ions

IUPAC: Encyclopedia II - IUPAC numerical multiplier - Compound affixes

The affix for a number larger than twelve is constructed is the opposite order to that which the number is written in Hindu-Arabic numerals: units, then tens, then hundreds, then thousands. For example: 548 → octa- (8) + tetraconta- (40) + pentacta- (500) = octatetracontapentacta- 9267 → hepta- (7) + hexaconta- (60) + dicta- (200) + nonalia- (9000) = heptahexacontadictanonalia- ...

See also:

IUPAC numerical multiplier, IUPAC numerical multiplier - Compound affixes, IUPAC numerical multiplier - The numeral one, IUPAC numerical multiplier - The numeral two, IUPAC numerical multiplier - Icosa- v. eicosa-, IUPAC numerical multiplier - Source

Read more here: » IUPAC numerical multiplier: Encyclopedia II - IUPAC numerical multiplier - Compound affixes

IUPAC: Encyclopedia II - IUPAC nomenclature of organic chemistry - Carboxylic acids

In general carboxylic acids are named with the suffix "-anoic acid". As for aldehydes, they take the "1" position on the parent chain, but do not have their position number indicated. For example, CH3CH2CH2CH2COOH (valeric acid) is named pentanoic acid. For common carboxylic acids some traditional names such as acetic acid are in such widespread use they are considered retained IUPAC names, although "systematic" names such as ethanoic acid are also acceptable. For carboxylic acids attached to a benze ...

See also:

IUPAC nomenclature of organic chemistry, IUPAC nomenclature of organic chemistry - Alkanes, IUPAC nomenclature of organic chemistry - Alkenes and Alkynes, IUPAC nomenclature of organic chemistry - Alcohols, IUPAC nomenclature of organic chemistry - Halogenated compounds, IUPAC nomenclature of organic chemistry - Ketones, IUPAC nomenclature of organic chemistry - Aldehydes, IUPAC nomenclature of organic chemistry - Carboxylic acids, IUPAC nomenclature of organic chemistry - Ethers, IUPAC nomenclature of organic chemistry - Esters, IUPAC nomenclature of organic chemistry - Amines and Amides, IUPAC nomenclature of organic chemistry - Cyclic compounds, IUPAC nomenclature of organic chemistry - Order of precedence of groups, IUPAC nomenclature of organic chemistry - Common nomenclature, IUPAC nomenclature of organic chemistry - Ketones, IUPAC nomenclature of organic chemistry - Aldehydes, IUPAC nomenclature of organic chemistry - Ions, IUPAC nomenclature of organic chemistry - Hydron, IUPAC nomenclature of organic chemistry - Parent hydride cations, IUPAC nomenclature of organic chemistry - Cations and substitution

Read more here: » IUPAC nomenclature of organic chemistry: Encyclopedia II - IUPAC nomenclature of organic chemistry - Carboxylic acids

IUPAC: Encyclopedia - Alkene

An alkene in organic chemistry is an unsaturated hydrocarbon containing at least one carbon to carbon double bond. The simplest alkenes, with only one double bond, form a homologous series, the alkenes with general formula CnH2n. The simplest alkene is C2H4, which has the common name "ethylene" and the International Union of Pure and Applied Chemistry (IUPAC) name "ethene". Alkenes are also called olefins and vinyl compounds. Alkene - Structure of AlkenesIncluding:

Read more here: » Alkene: Encyclopedia - Alkene

IUPAC: Encyclopedia II - IUPAC nomenclature of organic chemistry - Alkenes and Alkynes

Alkenes are named for their parent alkane chain with the suffix "-ene" and an infixed number indicating the position of the double-bonded carbon in the chain: CH2=CHCH2CH3 is but-1-ene. Ethene (ethylene) and propene (propylene) do not require infixed numbers, since there is no ambiguity in the structures. As before, the lowest number is used. Multiple double bonds take the form -diene, -triene, etc., with the size prefix of the chain taking an extra "a": CH2=CHCH=CH2 is buta-1,3-d ...

See also:

IUPAC nomenclature of organic chemistry, IUPAC nomenclature of organic chemistry - Alkanes, IUPAC nomenclature of organic chemistry - Alkenes and Alkynes, IUPAC nomenclature of organic chemistry - Alcohols, IUPAC nomenclature of organic chemistry - Halogenated compounds, IUPAC nomenclature of organic chemistry - Ketones, IUPAC nomenclature of organic chemistry - Aldehydes, IUPAC nomenclature of organic chemistry - Carboxylic acids, IUPAC nomenclature of organic chemistry - Ethers, IUPAC nomenclature of organic chemistry - Esters, IUPAC nomenclature of organic chemistry - Amines and Amides, IUPAC nomenclature of organic chemistry - Cyclic compounds, IUPAC nomenclature of organic chemistry - Order of precedence of groups, IUPAC nomenclature of organic chemistry - Common nomenclature, IUPAC nomenclature of organic chemistry - Ketones, IUPAC nomenclature of organic chemistry - Aldehydes, IUPAC nomenclature of organic chemistry - Ions, IUPAC nomenclature of organic chemistry - Hydron, IUPAC nomenclature of organic chemistry - Parent hydride cations, IUPAC nomenclature of organic chemistry - Cations and substitution

Read more here: » IUPAC nomenclature of organic chemistry: Encyclopedia II - IUPAC nomenclature of organic chemistry - Alkenes and Alkynes

IUPAC: Encyclopedia - Xylene

The term xylenes refers to a group of 3 benzene derivatives which encompasses ortho-, meta-, and para- isomers of dimethyl benzene. The o-, m- and p- isomers specify to which carbon atoms (of the main benzene ring) the two methyl groups are attached. Counting the carbon atoms from one of the ring carbons bonded to a methyl group, and counting towards the second ring carbon bonded to a methyl group, the o- isomer has the IUPAC name of 1,2-dimethylbenzene. The m- isomer has the IUPAC name of 1,3-dimethylbenzene. And p- isom ...

Including:

Read more here: » Xylene: Encyclopedia - Xylene

IUPAC: Encyclopedia - Group 11 element

A Group 11 element is the series of elements in group 11 (IUPAC style) in the periodic table, consisting of transition metals which are the traditional coinage metals of copper (Cu), silver (Ag), and gold (Au). They are also known as the "noble metals." The name "coinage metals" is not recognized by the International Union of Pure and Applied Chemistry (IUPAC), and can be somewhat misleading as further elements are added to the table. In addition, various nations have used probably dozens of metals (including stainless steel, lead, and zinc) in coins. The short-lived transactinid ...

Read more here: » Group 11 element: Encyclopedia - Group 11 element

IUPAC: Encyclopedia - Unique identifier

In order to get the full potential of knowledge, some organizations have started the process of sorting and structuring it up in a unique way, as to be able to identify, categorize and use it either for scientific, commercial or social purposes: Unique identifier - See Also. Systematic name Harmonized System WWPN Globally Unique Identifier Organizationally Unique Identifier Universally Unique Identifier Identifier Name Iupac nome ...

Including:

Read more here: » Unique identifier: Encyclopedia - Unique identifier

IUPAC: Encyclopedia - Butyric acid

Butyric acid, IUPAC name n-Butanoic acid, or normal butyric acid, is a carboxylic acid with structural formula CH3CH2CH2-COOH. It is notably found in rancid butter, parmesan cheese, or vomit and has an unpleasant odor and acrid taste, with a sweetish aftertaste (similar to ether). Butyric acid can be detected by mammals with good scent detection abilities (e.g. dogs) at 10 ppb, while h ...

Read more here: » Butyric acid: Encyclopedia - Butyric acid

IUPAC: Encyclopedia - Colistin

Image:Colistin.png polymyxin E IUPAC name ? CAS number ? ATC code A07AA10 / J01XB01 urine Indicated for: bacterial infections Contraindications: hypersensitivity to polymyxins Side effects: Severe: neurotoxic and nephrotoxic tubular necrosis deafness Atypical sensations: sensory disturbances of face and extremit ...

Including:

Read more here: » Colistin: Encyclopedia - Colistin

IUPAC: Encyclopedia - Acetyl

Acetyl (IUPAC name ethanoyl) is the acyl of acetic acid, with chemical formula -COCH3, sometimes abbreviated to Ac (not to be confused with the element actinium). A molecule containing an acetyl group has the chemical structure . (where R denotes the remainder of the molecule.) The acetyl radical contains a methyl group single-bonded to a carbonyl. The carbon of the carbonyl has an lone electron available, with which it forms a ch ...

Read more here: » Acetyl: Encyclopedia - Acetyl

IUPAC: Encyclopedia - Antiaromatic

Antiaromatic (or pseudoaromatic) molecules are cyclic systems containing alternating single and double bonds, where the pi electron energy of antiaromatic compounds is higher than that of its open-chain counterpart. Therefore antiaromatic compounds are unstable and highly reactive; often antiaromatic compounds distort themselves out of planarity to resolve this instability. Antiaromatic compounds usually fail the Hückel's rule of aromaticity. The IUPAC definition of antiaromatic compound: Compounds that contain 4n (n≠0) π-electrons in a cyclic planar, or nearly planar, ...

Including:

Read more here: » Antiaromatic: Encyclopedia - Antiaromatic

IUPAC: Encyclopedia - Carbon-12

Carbon-12 is the more abundant (98.89%) of the two stable isotopes of the element carbon. It contains 6 protons, 6 neutrons and 6 electrons. Carbon-12 is of particular importance as it is used as the standard from which all other isotopes' atomic weight is measured and thus the measurement of Avogadro's number. Carbon-12 - History. Prior to 1959 both the IUPAP and IUPAC tended to use used oxygen to define the mole, the chemists defining the mole as the number of atoms of oxygen which had mass ...

Including:

Read more here: » Carbon-12: Encyclopedia - Carbon-12

IUPAC: Encyclopedia - Haloalkane

The haloalkanes (also known as Halogenoalkanes) are a group of chemical compounds, consisting of alkanes, such as methane or ethane, with one or more halogens linked, such as chlorine or fluorine, making them a type of organic halide. They are known under many chemical and trivial names. As fire extinguishers, propellants, and solvents, they have or had wide use. Some haloalkanes have negative effects on the environment, such as ozone depletion. Haloalkane - General. A haloalkane, also known as al ...

Including:

Read more here: » Haloalkane: Encyclopedia - Haloalkane

IUPAC: Encyclopedia - Alkali metal

The alkali metals are the series of elements in Group 1 (IUPAC style) of the periodic table, excluding hydrogen: that is, lithium (Li), sodium (Na), potassium (K), rubidium (Rb), caesium (Cs), and francium (Fr). They are all highly reactive and are never found in elemental form in nature. The alkali metals are silver-colored, soft, low-density metals, which react readily with halogens to form ionic salts, and with water to form strongly alkaline (basic) hydroxides. These elements all ha ...

Read more here: » Alkali metal: Encyclopedia - Alkali metal

IUPAC: Encyclopedia - Alkaline earth metal

The alkaline earth metals are the series of elements in Group 2 (IUPAC style) of the periodic table: beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), barium (Ba) and radium (Ra) (not always considered due to its radioactivity and very short half-life). The alkaline earth metals are named after their oxides, the alkaline earths, whose old-fashioned names were beryllia, magnesia, lime, strontia and baryta. These were named alkaline earths because of their interm ...

Read more here: » Alkaline earth metal: Encyclopedia - Alkaline earth metal

IUPAC: Encyclopedia - Amine

Amines are organic compounds containing nitrogen as the key atom in the amine functional group. Amines have structures resembling ammonia, where one or more hydrogen atoms are replaced by alkyl groups or other groups where the nitrogen is bonded to a carbon atom in the group (groups symbolized by R below). However, if any of the carbons bonded to the nitrogen that is part of a carbonyl group, then the compound is considered an amide rather than an amine. See the Category:Amines for a list of types of amine and some real examp ...

Including:

Read more here: » Amine: Encyclopedia - Amine

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