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In chemical nomenclature, the IUPAC nomenclature of inorganic chemistry is a systematic method of naming inorganicchemical compounds, as recommended by the International Union of Pure and Applied Chemistry (IUPAC). It is published in Nomenclature of Inorganic Chemistry (which is informally called the Red Book).^[1] Ideally, every inorganic compound should have a name from which an unambiguous formula can be determined. There is also an IUPAC nomenclature of organic chemistry.

Iupac Nomenclature Rules With Examples Pdf

Vide basic rules and examples for naming monofunctional compounds. However, students of more advanced organic chemistry courses and graduate students dealing with more complex molecules need a set of additional rules and guide-lines to identify polyfunctional compounds. The following summary of general principles may also be useful to instruc-tors. Aug 12, 2019  Nomenclature of Alcohols Alcohols with one to four carbon atoms are frequently called by common names, in which the name of the alkyl group is followed by the word alcohol: According to the International Union of Pure and Applied Chemistry (IUPAC), alcohols are named by changing the ending of the parent alkane name to - ol.

Iupac Nomenclature Rules Pdf Download

• 2Traditional naming
  • 2.1Naming simple ionic compounds
  • 2.3Naming molecular compounds

System[edit]

The names 'caffeine' and '3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione' both signify the same chemical. 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' just names it. These advantages make the systematic name far superior to the common name when absolute clarity and precision are required. However, for the sake of brevity, even professional chemists will use the non-systematic name almost all of the time, because caffeine is a well-known common chemical with a unique structure. Similarly, H₂O is most often simply called water in English, though other chemical names do exist.

1. Single atom anions are named with an -ide suffix: for example, H⁻ is hydride.
2. Compounds with a positive ion (cation): The name of the compound is simply the cation's name (usually the same as the element's), followed by the anion. For example, NaCl is sodium chloride, and CaF₂ is calcium fluoride.
3. Cations which have taken on more than one positive charge are labeled with Roman numerals in parentheses. For example, Cu⁺ is copper(I), Cu²⁺ is copper(II). An older, deprecated notation is to append -ous or -ic to the root of the Latin name to name ions with a lesser or greater charge. Under this naming convention, Cu⁺ is cuprous and Cu²⁺ is cupric. For naming metal complexes see the page on complex (chemistry).
4. Oxyanions (polyatomic anions containing oxygen) are named with -ite or -ate, for a lesser or greater quantity of oxygen, respectively. For example, NO⁻
   ₂ is nitrite, while NO⁻
   ₃ is nitrate. If four oxyanions are possible, the prefixes hypo- and per- are used: hypochlorite is ClO⁻, perchlorate is ClO⁻
   ₄.
5. The prefix bi- is a deprecated way of indicating the presence of a single hydrogen ion, as in 'sodium bicarbonate' (NaHCO₃). The modern method specifically names the hydrogen atom. Thus, NaHCO₃ would be pronounced sodium hydrogen carbonate.

Positively charged ions are called cations and negatively charged ions are called anions. The cation is always named first. Ions can be metals, non-metals or polyatomic ions. Therefore, the name of the metal or positive polyatomic ion is followed by the name of the non-metal or negative polyatomic ion. The positive ion retains its element name whereas for a single non-metal anion the ending is changed to -ide.

Example: sodium chloride, potassium oxide, or calcium carbonate.

When the metal has more than one possible ionic charge or oxidation number the name becomes ambiguous. In these cases the oxidation number (the same as the charge) of the metal ion is represented by a Roman numeral in parentheses immediately following the metal ion name. For example, in uranium(VI) fluoride the oxidation number of uranium is 6. Another example is the iron oxides. FeO is iron(II) oxide and Fe₂O₃ is iron(III) oxide.

An older system used prefixes and suffixes to indicate the oxidation number, according to the following scheme:

Thus the four oxyacids of chlorine are called hypochlorous acid (HOCl), chlorous acid (HOClO), chloric acid (HOClO₂) and perchloric acid (HOClO₃), and their respective conjugate bases are the hypochlorite, chlorite, chlorate and perchlorate ions. This system has partially fallen out of use, but survives in the common names of many chemical compounds: the modern literature contains few references to 'ferric chloride' (instead calling it 'iron(III) chloride'), but names like 'potassium permanganate' (instead of 'potassium manganate(VII)') and 'sulfuric acid' abound.

Traditional naming[edit]

Naming simple ionic compounds[edit]

An ionic compound is named by its cation followed by its anion. See polyatomic ion for a list of possible ions.

For cations that take on multiple charges, the charge is written using Roman numerals in parentheses immediately following the element name. For example, Cu(NO₃)₂ is copper(II) nitrate, because the charge of two nitrate ions (NO⁻
₃) is 2 × −1 = −2, and since the net charge of the ionic compound must be zero, the Cu ion has a 2+ charge. This compound is therefore copper(II) nitrate. In the case of cations with a +4 oxidation state, the only acceptable format for the Roman numeral 4 is IV and not IIII.

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], for more details see selected pages from IUPAC rules for naming inorganic compounds.

List of common ion names[edit]

Monatomic anions:

Cl⁻
chloride

S²⁻
sulfide

P³⁻
phosphide

Polyatomic ions:

NH⁺
₄ammonium

H
₃O⁺
hydronium

NO⁻
₃nitrate

NO⁻
₂nitrite

ClO⁻
hypochlorite

ClO⁻
₂chlorite

ClO⁻
₃chlorate

ClO⁻
₄perchlorate

SO²⁻
₃sulfite

SO²⁻
₄sulfate

HSO⁻
₃hydrogen sulfite (or bisulfite)

HCO⁻
₃hydrogen carbonate (or bicarbonate)

CO²⁻
₃carbonate

PO³⁻
₄phosphate

HPO²⁻
₄hydrogen phosphate

H
₂PO⁻
₄dihydrogen phosphate

CrO²⁻
₄chromate

Cr
₂O²⁻
₇dichromate

BO³⁻
₃borate

AsO³⁻
₄arsenate

C
₂O²⁻
₄oxalate

CN⁻
cyanide

SCN⁻
thiocyanate

MnO⁻
₄permanganate

Naming hydrates[edit]

Hydrates are ionic compounds that have absorbed water. They are named as the ionic compound followed by a numerical prefix and -hydrate. The numerical prefixes used are listed below (see IUPAC numerical multiplier):

For example, CuSO₄·5H₂O is 'copper(II) sulfate pentahydrate'.

Naming molecular compounds[edit]

Inorganic molecular compounds are named with a prefix (see list above) before each element. The more electronegative element is written last and with an -ide suffix. For example, H₂O (water) can be called dihydrogen monoxide. Organic molecules do not follow this rule. In addition, the prefix mono- is not used with the first element; for example, SO₂ is sulfur dioxide, not 'monosulfur dioxide'. Sometimes prefixes are shortened when the ending vowel of the prefix 'conflicts' with a starting vowel in the compound. This makes the name easier to pronounce; for example, CO is 'carbon monoxide' (as opposed to 'monooxide').

Common exceptions[edit]

There are a number of exceptions and special cases that violate the above rules. Sometimes the prefix is left off of the initial atom: I₂O₅ is known as iodine pentoxide, but it should be called diiodine pentoxide. N₂O₃ is called nitrogen sesquioxide (sesqui- means ​1¹⁄₂).

The main oxide of phosphorus is called phosphorus pentoxide. It should actually be diphosphorus pentoxide, but it is assumed that there are two phosphorus atoms (P₂O₅), as they are needed in order to balance the oxidation numbers of the five oxygen atoms. However, people have known for years that the real form of the molecule is P₄O₁₀, not P₂O₅, yet it is not normally called tetraphosphorus decaoxide.

In writing formulas, ammonia is NH₃ even though nitrogen is more electronegative (in line with the convention used by IUPAC as detailed in Table VI of the red book). Likewise, methane is written as CH₄ even though carbon is more electronegative (Hill system).

Nomenclature of Inorganic Chemistry[edit]

Nomenclature of Inorganic Chemistry, commonly referred to by chemists as the Red Book, is a collection of recommendations on IUPAC nomenclature, published at irregular intervals by the IUPAC. The last full edition was published in 2005,^[2] in both paper and electronic versions.

See also[edit]

• IUPAC nomenclature of inorganic chemistry 2005 (the Red Book)
• Nomenclature of Organic Chemistry (the Blue Book)
• Quantities, Units and Symbols in Physical Chemistry (the Green Book)
• Compendium of Chemical Terminology (the Gold Book)
• Compendium of Analytical Nomenclature (the Orange Book)

References[edit]

1. ^Nomenclature of Inorganic Chemistry IUPAC Recommendations 2005 - Full text (PDF)
   2004 version with separate chapters as pdf: IUPAC Provisional Recommendations for the Nomenclature of Inorganic Chemistry (2004)Archived 2008-02-19 at the Wayback Machine
2. ^International Union of Pure and Applied Chemistry (2005). Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005). Cambridge (UK): RSC–IUPAC. ISBN0-85404-438-8. Electronic version.

External links[edit]

• Bibliography of IUPAC Recommendations on Inorganic Nomenclature (last updated 17 February 2004)
• IUPAC Nomenclature Books Series (commonly known as the 'Colour Books')

In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a systematic method of naming organic chemical compounds as recommended^[1] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). Ideally, every possible organic compound should have a name from which an unambiguous structural formula can be created. There is also an IUPAC nomenclature of inorganic chemistry.

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 molecules they can be more easily understood than non-systematic names, which must be learnt or looked up. However, the common or trivial name is often substantially shorter and clearer, and so preferred. These non-systematic names are often derived from an original source of the compound. In addition, very long names may be less clear than structural formulae.

• 2Hydrocarbons
• 3Functional groups
• 5Common nomenclature – trivial names
• 6Ions
• 8References

Basic principles[edit]

In chemistry, a number of prefixes, suffixes and infixes are used to describe the type and position of functional groups in the compound.

The steps for naming an organic compound are:

1. Identification of the parent hydrocarbon chain. This chain must obey the following rules, in order of precedence:
   1. It should have the maximum number of substituents of the suffix functional group. By suffix, it is meant that the parent functional group should have a suffix, unlike halogen substituents. If more than one functional group is present, the one with highest precedence should be used.
   2. It should have the maximum number of multiple bonds.
   3. It should have the maximum number of single bonds.
   4. It should have the maximum length.
2. Identification of the parent functional group, if any, with the highest order of precedence.
3. Identification of the side-chains. Side chains are the carbon chains that are not in the parent chain, but are branched off from it.
4. Identification of the remaining functional groups, if any, and naming them by their ionic prefixes (such as hydroxy for -OH, oxy for =O, oxyalkane for O-R, etc.).
   Different side-chains and functional groups will be grouped together in alphabetical order. (The prefixes di-, tri-, etc. are not taken into consideration for grouping alphabetically. For example, ethyl comes before dihydroxy or dimethyl, as the 'e' in 'ethyl' precedes the 'h' in 'dihydroxy' and the 'm' in 'dimethyl' alphabetically. The 'di' is not considered in either case). When both side chains and secondary functional groups are present, they should be written mixed together in one group rather than in two separate groups.
5. Identification of double/triple bonds.
6. Numbering of the chain. This is done by first numbering the chain in both directions (left to right and right to left), and then choosing the numbering which follows these rules, in order of precedence
   1. Has the lowest-numbered locant (or locants) for the suffix functional group. Locants are the numbers on the carbons to which the substituent is directly attached.
   2. Has the lowest-numbered locants for multiple bonds (The locant of a multiple bond is the number of the adjacent carbon with a lower number).
   3. Has the lowest-numbered locants for prefixes.
7. Numbering of the various substituents and bonds with their locants. If there is more than one of the same type of substituent/double bond, a prefix is added showing how many there are ( di – 2 tri – 3 tetra – 4 then as for the number of carbons below with 'a' added)

The numbers for that type of side chain will be grouped in ascending order and written before the name of the side-chain. If there are two side-chains with the same alpha carbon, the number will be written twice. Example: 2,2,3-trimethyl- . If there are both double bonds and triple bonds, 'en' (double bond) is written before 'yne' (triple bond). When the main functional group is a terminal functional group (a group which can exist only at the end of a chain, like formyl and carboxyl groups), there is no need to number it.

1. Arrangement in this form: Group of side chains and secondary functional groups with numbers made in step 3 + prefix of parent hydrocarbon chain (eth, meth) + double/triple bonds with numbers (or 'ane') + primary functional group suffix with numbers.
   Wherever it says 'with numbers', it is understood that between the word and the numbers, the prefix(di-, tri-) is used.
2. Adding of punctuation:
   1. Commas are put between numbers (2 5 5 becomes 2,5,5)
   2. Hyphens are put between a number and a letter (2 5 5 trimethylheptane becomes 2,5,5-trimethylheptane)
   3. Successive words are merged into one word (trimethyl heptane becomes trimethylheptane)
      Note: IUPAC uses one-word names throughout. This is why all parts are connected.

The finalized name should look like this:
#,#-di<side chain>-#-<secondary functional group>-#-<side chain>-#,#,#-tri<secondary functional group><parent chain prefix><If all bonds are single bonds, use 'ane'>-#,#-di<double bonds>-#-<triple bonds>-#-<primary functional group>
Note: # is used for a number. The group secondary functional groups and side chains may not look the same as shown here, as the side chains and secondary functional groups are arranged alphabetically. The di- and tri- have been used just to show their usage. (di- after #,#, tri- after #,#,#, etc.)

Example

Here is a sample molecule with the parent carbons numbered:

For simplicity, here is an image of the same molecule, where the hydrogens in the parent chain are removed and the carbons are shown by their numbers:

Now, following the above steps:

1. The parent hydrocarbon chain has 23 carbons. It is called tricosa-.
2. The functional groups with the highest precedence are the two ketone groups.
   1. The groups are on carbon atoms 3 and 9. As there are two, we write 3,9-dione.
   2. The numbering of the molecule is based on the ketone groups. When numbering from left to right, the ketone groups are numbered 3 and 9. When numbering from right to left, the ketone groups are numbered 15 and 21. 3 is less than 15, therefore the ketones are numbered 3 and 9. The smaller number is always used, not the sum of the constituents numbers.
3. The side chains are: an ethyl- at carbon 4, an ethyl- at carbon 8, and a butyl- at carbon 12.
   Note:The -O-CH₃ at carbon atom 15 is not a side chain, but it is a methoxy functional group.
   • There are two ethyl- groups. They are combined to create, 4,8-diethyl.
   • The side chains are grouped like this: 12-butyl-4,8-diethyl. (But this is not necessarily the final grouping, as functional groups may be added in between to ensure all groups are listed alphabetically.)
4. The secondary functional groups are: a hydroxy- at carbon 5, a chloro- at carbon 11, a methoxy- at carbon 15, and a bromo- at carbon 18. Grouped with the side chains, this gives 18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxy.
5. There are two double bonds: one between carbons 6 and 7, and one between carbons 13 and 14. They would be called '6,13-diene', but the presence of alkynes switches it to 6,13-dien. There is one triple bond between carbon atoms 19 and 20. It will be called 19-yne.
6. The arrangement (with punctuation) is: 18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxytricosa-6,13-dien-19-yne-3,9-dione
7. Finally, due to cis-trans isomerism, we have to specify the relative orientation of functional groups around each double bond. For this example, we have (6E,13E)

The final name is (6E,13E)-18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxytricosa-6,13-dien-19-yne-3,9-dione.

Hydrocarbons[edit]

Alkanes[edit]

Straight-chain alkanes take the suffix '-ane' and are prefixed depending on the number of carbon atoms in the chain, following standard rules. The first few are:

For example, the simplest alkane is CH₄ methane, and the nine-carbon alkane CH₃(CH₂)₇CH₃ is named nonane. The names of the first four alkanes were derived from methanol, ether, propionic acid and butyric acid, respectively. The rest are named with a Greek numeric prefix, with the exceptions of nonane which has a Latin prefix, and undecane and tridecane which have mixed-language prefixes.

Cyclic alkanes are simply prefixed with 'cyclo-': for example, C₄H₈ is cyclobutane (not to be confused with butene) and C₆H₁₂ is cyclohexane (not to be confused with hexene).

Branched alkanes are named as a straight-chain alkane with attached alkyl groups. They are prefixed with a number indicating the carbon the group is attached to, counting from the end of the alkane chain. For example, (CH₃)₂CHCH₃, commonly known as isobutane, is treated as a propane chain with a methyl group bonded to the middle (2) carbon, and given the systematic name 2-methylpropane. However, although the name 2-methylpropane could be used, it is easier and more logical to call it simply methylpropane – the methyl group could not possibly occur on any of the other carbon atoms (that would lengthen the chain and result in butane, not propane) and therefore the use of the number '2' is unnecessary.

If there is ambiguity in the position of the substituent, depending on which end of the alkane chain is counted as '1', then numbering is chosen so that the smaller number is used. For example, (CH₃)₂CHCH₂CH₃ (isopentane) is named 2-methylbutane, not 3-methylbutane.

If there are multiple side-branches of the same size alkyl group, their positions are separated by commas and the group prefixed with di-, tri-, tetra-, etc., depending on the number of branches. For example, C(CH₃)₄ (neopentane) is named 2,2-dimethylpropane. If there are different groups, they are added in alphabetical order, separated by commas or hyphens: . The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).

Alkenes[edit]

Alkenes are named for their parent alkane chain with the suffix '-ene' and an infixed number indicating the position of the carbon with the lower number for each double bond in the chain: CH₂=CHCH₂CH₃ is but-1-ene.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-diene. Simple cis and transisomers may be indicated with a prefixed cis- or trans-: cis-but-2-ene, trans-but-2-ene. However, cis- and trans- are relative descriptors. It is IUPAC convention to describe all alkenes using absolute descriptors of Z- (same side) and E- (opposite) with the Cahn–Ingold–Prelog priority rules.

Alkynes[edit]

Alkynes are named using the same system, with the suffix '-yne' indicating a triple bond: ethyne (acetylene), propyne (methylacetylene).

Functional groups[edit]

Haloalkanes and Haloarenes[edit]

In Haloalkanes and Haloarenes (R-X), Halogen functional groups are prefixed with the bonding position and take the form of fluoro-, chloro-, bromo-, iodo-, etc., depending on the halogen. Multiple groups are dichloro-, trichloro-, etc., and dissimilar groups are ordered alphabetically as before. For example, CHCl₃ (chloroform) is trichloromethane. The anesthetic Halothane (CF₃CHBrCl) is 2-bromo-2-chloro-1,1,1-trifluoroethane.

Alcohols[edit]

Alcohols (R-OH) take the suffix '-ol' with an infix numerical bonding position: CH₃CH₂CH₂OH is propan-1-ol. The suffixes -diol, -triol, -tetraol, etc., are used for multiple -OH groups: Ethylene glycol CH₂OHCH₂OH is ethane-1,2-diol.

If higher precedence functional groups are present (see order of precedence, below), the prefix 'hydroxy' is used with the bonding position: CH₃CHOHCOOH is 2-hydroxypropanoic acid.

Ethers[edit]

Ethers (R-O-R) consist of an oxygen atom between the two attached carbon chains. The shorter of the two chains becomes the first part of the name with the -ane suffix changed to -oxy, and the longer alkane chain becomes the suffix of the name of the ether. Thus, CH₃OCH₃ is methoxymethane, and CH₃OCH₂CH₃ is methoxyethane (not ethoxymethane). If the oxygen is not attached to the end of the main alkane chain, then the whole shorter alkyl-plus-ether group is treated as a side-chain and prefixed with its bonding position on the main chain. Thus CH₃OCH(CH₃)₂ is 2-methoxypropane.

Alternatively, an ether chain can be named as an alkane in which one carbon is replaced by an oxygen, a replacement denoted by the prefix 'oxa'. For example, CH₃OCH₂CH₃ could also be called 2-oxabutane, and an epoxide could be called oxacyclopropane. This method is especially useful when both groups attached to the oxygen atom are complex.^[2]

Aldehydes[edit]

Aldehydes (R-CHO) take the suffix '-al'. If other functional groups are present, the chain is numbered such that the aldehyde carbon is in the '1' position, unless functional groups of higher precedence are present.

If a prefix form is required, 'oxo-' is used (as for ketones), with the position number indicating the end of a chain: CHOCH₂COOH is 3-oxopropanoic acid. If the carbon in the carbonyl group cannot be included in the attached chain (for instance in the case of cyclic aldehydes), the prefix 'formyl-' or the suffix '-carbaldehyde' is used: C₆H₁₁CHO is cyclohexanecarbaldehyde. If an aldehyde is attached to a benzene and is the main functional group, the suffix becomes benzaldehyde.

Ketones[edit]

In general ketones (R-CO-R) take the suffix '-one' (pronounced own, not won) with an infix position number: CH₃CH₂CH₂COCH₃ is pentan-2-one. If a higher precedence suffix is in use, the prefix 'oxo-' is used: CH₃CH₂CH₂COCH₂CHO is 3-oxohexanal.

Carboxylic acids[edit]

In general, carboxylic acids are named with the suffix -oic acid (etymologically a back-formation from benzoic acid). As with aldehydes, the carboxyl functional group must take the '1' position on the main chain and so the locant need not be stated. For example, CH₃-CH(OH)-COOH (lactic acid) is named 2-hydroxypropanoic acid with no '1' stated. Some traditional names for common carboxylic acids (such as acetic acid) are in such widespread use that they are retained in IUPAC nomenclature,^[3] though systematic names like ethanoic acid are also used. Carboxylic acids attached to a benzene ring are structural analogs of benzoic acid (Ph-COOH) and are named as one of its derivatives.

If there are multiple carboxyl groups on the same parent chain, multiplying prefixes are used: Malonic acid, CH
₂(COOH)
₂, is systematically named propanedioic acid. Alternatively, the suffix '-carboxylic acid' can be used, combined with a multiplying prefix if necessary – mellitic acid is benzenehexacarboxylic acid, for example. In the latter case, the carbon atom(s) in the carboxyl group(s) do not count as being part of the main chain, a rule that also applies to the prefix form 'carboxy-'. Citric acid serves as an example: it is formally named 2-hydroxypropane-1,2,3-tricarboxylic acid rather than 3-carboxy-3-hydroxypentanedioic acid.

Iupac Naming Chart

Carboxylates[edit]

Salts of carboxylic acids are named following the usual cation-then-anion conventions used for ionic compounds in both IUPAC and common nomenclature systems. The name of the carboxylate anion is derived from that of the parent acid by replacing the '–oic acid' ending with '–oate.' For example, C
₆H
₅CO
₂Na, the sodium salt of benzoic acid (C
₆H
₅COOH), is called sodium benzoate. Where an acid has both a systematic and a common name (like CH
₃COOH, for example, which is known as both acetic acid and as ethanoic acid), its salts can be named from either parent name. Thus, CH
₃CO
₂K can be named as potassium acetate or as potassium ethanoate.

Esters[edit]

Esters (R-CO-O-R') are named as alkyl derivatives of carboxylic acids. The alkyl (R') group is named first. The R-CO-O part is then named as a separate word based on the carboxylic acid name, with the ending changed from -oic acid to -oate. For example, CH₃CH₂CH₂CH₂COOCH₃ is methyl pentanoate, and (CH₃)₂CHCH₂CH₂COOCH₂CH₃ is ethyl 4-methylpentanoate. For esters such as ethyl acetate (CH₃COOCH₂CH₃), ethyl formate (HCOOCH₂CH₃) or dimethyl phthalate that are based on common acids, IUPAC recommends use of these established names, called retained names. The -oate changes to -ate. Some simple examples, named both ways, are shown in the figure above.

If the alkyl group is not attached at the end of the chain, the bond position to the ester group is infixed before '-yl': CH₃CH₂CH(CH₃)OOCCH₂CH₃ may be called but-2-yl propanoate or but-2-yl propionate.^{[citation needed]}

Acyl Groups[edit]

Acyl groups are named by stripping the -ic acid of the corresponding carboxylic acid and replacing it with -yl. For Example, CH3CO-R is called Ethanoyl-R.

Acyl Halides[edit]

Simply add the name of the attached halide to the end of the acyl group. For example, CH3COCl is Ethanoyl Chloride.

Acid Anhydrides[edit]

If both acyl groups are the same, then the name of the carboxylic acid with the word acid replaced with anhydride. If the acyl groups are different, then they are named in alphabetical order in the same way, with anhydride replacing acid. For example, CH3CO-O-OCCH3 is called Ethanoic Anhydride.

Amines[edit]

Amines (R-NH₂) are named for the attached alkane chain with the suffix '-amine' (e.g. CH₃NH₂ methanamine). If necessary, the bonding position is infixed: CH₃CH₂CH₂NH₂ propan-1-amine, CH₃CHNH₂CH₃ propan-2-amine. The prefix form is 'amino-'.

For secondary amines (of the form R-NH-R), the longest carbon chain attached to the nitrogen atom becomes the primary name of the amine; the other chain is prefixed as an alkyl group with location prefix given as an italic N: CH₃NHCH₂CH₃ is N-methylethanamine. Tertiary amines (R-NR-R) are treated similarly: CH₃CH₂N(CH₃)CH₂CH₂CH₃ is N-ethyl-N-methylpropanamine. Again, the substituent groups are ordered alphabetically.

Amides[edit]

Amides (R-CO-NH₂) take the suffix '-amide', or '-carboxamide' if the carbon in the amide group cannot be included in the main chain. The prefix form is both 'carbamoyl-' and 'amido-'.

Amides that have additional substituents on the nitrogen are treated similarly to the case of amines: they are ordered alphabetically with the location prefix N: HCON(CH₃)₂ is N,N-dimethylmethanamide.

Nitriles[edit]

Nitriles (RCN) are named by adding the suffix -nitrile to the longest hydrocarbon chain (including the carbon of the cyano group). It can also be named by replacing the -oic acid of their corresponding carboxylic acids with -onitrile. Functional class IUPAC nomenclature may also be used in the form of alkyl cyanides. For example, CH3CH2CH2CH2CN is called pentanenitrile or butyl cyanide.

Cyclic compounds[edit]

Cycloalkanes and aromatic compounds can be treated as the main parent chain of the compound, in which case the positions of substituents are numbered around the ring structure. For example, the three isomers of xylene CH₃C₆H₄CH₃, commonly the ortho-, meta-, and para- forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix 'cycloalkyl-' (e.g. 'cyclohexyl-') or for benzene, 'phenyl-'.

The IUPAC nomenclature scheme becomes rapidly more elaborate for more complex cyclic structures, with notation for compounds containing conjoined rings, and many common names such as phenol being accepted as base names for compounds derived from them.

Order of precedence of groups[edit]

When compounds contain more than one functional group, the order of precedence determines which groups are named with prefix or suffix forms. The table below shows common groups in decreasing order of precedence. The highest-precedence group takes the suffix, with all others taking the prefix form. However, double and triple bonds only take suffix form (-en and -yn) and are used with other suffixes.

Prefixed substituents are ordered alphabetically (excluding any modifiers such as di-, tri-, etc.), e.g. chlorofluoromethane, not fluorochloromethane. If there are multiple functional groups of the same type, either prefixed or suffixed, the position numbers are ordered numerically (thus ethane-1,2-diol, not ethane-2,1-diol.) The N position indicator for amines and amides comes before '1', e.g. CH₃CH(CH₃)CH₂NH(CH₃) is N,2-dimethylpropanamine.

*Note: These suffixes, in which the carbon atom is counted as part of the preceding chain, are the most commonly used. See individual functional group articles for more details.

The order of remaining functional groups is only needed for substituted benzene and hence is not mentioned here.^{[clarification needed]}

Common nomenclature – trivial names[edit]

Common nomenclature uses the older names for some organic compounds instead of using the prefixes for the carbon skeleton above. The pattern can be seen below.

Ketones[edit]

Common names for ketones can be derived by naming the two alkyl or aryl groups bonded to the carbonyl group as separate words followed by the word ketone.

The first three of the names shown above are still considered to be acceptable IUPAC names.

Aldehydes[edit]

The common name for an aldehyde is derived from the common name of the corresponding carboxylic acid by dropping the word acid and changing the suffix from -ic or -oic to -aldehyde.

Ions[edit]

The IUPAC nomenclature also provides rules for naming ions.

Hydron[edit]

Hydron is a generic term for hydrogen cation; protons, deuterons and tritons are all hydrons.The Hydrons are not found in heavier isotopes, however.

Parent hydride cations[edit]

Simple cations formed by adding a hydron to a hydride of a halogen, chalcogen or pnictogen are named by adding the suffix '-onium' to the element's root: H₄N⁺ is ammonium, H₃O⁺ is oxonium, and H₂F⁺ is fluoronium. Ammonium was adopted instead of nitronium, which commonly refers to NO₂⁺.

If the cationic center of the hydride is not a halogen, chalcogen or pnictogen then the suffix '-ium' is added to the name of the neutral hydride after dropping any final 'e'. H₅C⁺ is methanium, HO-(O⁺)-H₂ is dioxidanium (HO-OH is dioxidane), and H₂N-(N⁺)-H₃ is diazanium (H₂N-NH₂ is diazane).

Cations and substitution[edit]

The above cations except for methanium are not, strictly speaking, organic, since they do not contain carbon. However, many organic cations are obtained by substituting another element or some functional group for a hydrogen.

The name of each substitution is prefixed to the hydride cation name. If many substitutions by the same functional group occur, then the number is indicated by prefixing with 'di-', 'tri-' as with halogenation. (CH₃)₃O⁺ is trimethyloxonium. CH₃F₃N⁺ is trifluoromethylammonium.

See also[edit]

References[edit]

1. ^The Commission on the Nomenclature of Organic Chemistry (1971) [1958 (A: Hydrocarbons, and B: Fundamental Heterocyclic Systems), 1965 (C: Characteristic Groups)]. Nomenclature of Organic Chemistry (3rd edition combined ed.). London: Butterworths. ISBN0-408-70144-7.
2. ^'Basic IUPAC Organic Nomenclature'.
3. ^International Union of Pure and Applied Chemistry Organic Chemistry Division Commission on Nomenclature of Organic Chemistry (1995). 'Table 28(a): Carboxylic acids and related group'. In Panico, Robert; Powell, Warren H.; Richer, Jean-Claude (eds.). A Guide to IUPAC Nomenclature of Organic Compounds: Recommendations 1993 (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of Organic Chemistry) (2nd ed.). Oxford: Blackwell Scientific Publications. ISBN9780632034888.

Bibliography[edit]

• Favre, Henri A.; Powell, Warren H. (2013). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. Royal Society of Chemistry. ISBN978-0-85404-182-4.

External links[edit]

• IUPAC Nomenclature of Organic Chemistry (online version of several older editions of the IUPAC Blue Book)
• IUPAC Recommendations on Organic & Biochemical Nomenclature, Symbols, Terminology, etc. (includes IUBMB Recommendations for biochemistry)
• Bibliography of IUPAC Recommendations on Organic Nomenclature (last updated 11 April 2003)
• ACD/Name Software for generating systematic nomenclature
• ChemAxon Name <> Structure – ChemAxon IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at chemicalize.org
• chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.
• Eller, Gernot A. (2006). 'Improving the Quality of Published Chemical Names with Nomenclature Software'(PDF). Molecules. 9: 915–928.
• Leigh, G. J.; Favre, H. A.; Metanomski, W. V. (1998). Principles of Chemical Nomenclature. A Guide to IUPAC Recommendations(PDF). Blackwell.