IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (2024)

  • Chemist Notes
  • September 19, 2023
  • General Organic Chemistry

Table of Contents

Organic chemists developed and utilized the IUPAC nomenclature system of organic compounds to solve the problems caused by common/arbitrary nomenclature systems. The comprehensive and systematic set of logical rules for the nomenclature of organic compounds was prepared by IUPAC (International Union of Pure and Applied Chemistry) in 1979 and was upgraded in 1993.

IUPAC nomenclature of organic compounds

Before going to the rules of the IUPAC nomenclature system of organic compounds, let’s discuss some terms involved in it.

IUPAC Name= Prefix + Word root + Primary suffix + Secondary suffix

Prefix: The word prefix means the substituents or groups written before the word root. Side chains, substituents, and low-priority functional groups are written as prefixes. All the atoms or groups except the principal functional group present in the parent chain are written before the word root and called substituents or prefixes.

Word root: The word root indicates the total number of carbon atoms in the longest continuous carbon chain, also known as the parent chain. The word root of the organic compound denotes the name of alkanes and cycloalkanes.

No. of Carbon atomsWord rootNo. of Carbon atomsWord root
C1Meth-C20Eicos-
C2Eth-C30Triacont-
C3Prop-C40Tetracont-
C4But-C50Pentacont-
C5Pent-C60Hexacont-
C6Hex-C70Heptacont-
C7Hept/Sept-C80Octacont-
C8Oct-C90Nonacont-
C9Non-C100Hect-
C10Dec-

Primary Suffix: Primary suffix indicates the type of carbon-carbon bond present or the saturated or unsaturated nature of the longest chain or parent chain.

Nature/Type of C-C bondPrimary Suffix
C-C-ane
C=C-ene
C≡C-yne

If more than one carbon-carbon double bond or triple bond is present in the parent chain the di- is used for 2, tri- for three, tetra- for four, and so on is written before the primary suffix along with their positions.

Secondary Suffix: The secondary suffix indicates the principal functional group present in the parent chain and is written immediately after the primary suffix. If the secondary suffix starts with a vowel letter then the ‘e’ of the primary suffix is replaced by the secondary suffix.

Rules of IUPAC Nomenclature

IUPAC has proposed some rules for the nomenclature of organic compounds which are as follows:

1. Longest chain rule (selection of longest continuous carbon chain)

Always select the longest possible continuous carbon chain which determines the word root and primary suffix.

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (1)

If two or more equal long chains are possible then that chain is selected which has more numbers of side chains or prefixes.

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (2)

2. Lowest Number rule

This rule is applied only when only one substituent is present in the parent chain (longest chain). The numbering is started from that end which gives the lowest number to the substituent attached to the parent chain, i.e., the numbering should be started from the close end of the substituent.

Alkyl groups attached to the longest chain are called substituents and are written as prefixes.

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (3)

3. Lowest sum rule

If more than one same substituent is present in the parent chain the number should be started from that end which gives the lowest sum of numbers assigned to substituents attached to the parent chain.

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (4)

4. Alphabetical order rule (Naming of substituents)

When two or more different substituents are present in the parent chain, then the substituents must be written in alphabetical order. Substituents are written as prefix and their positions are indicated by separate numbers.

  • If two or more same substituents are present in the parent chain then di-, tri-, tetra-, etc. are used and their positions are separated by a comma, (,). For comparison in alphabetical order prefixes, di-, tri- etc. are not considered.
  • If different substituents/prefixes are present on the parent chain then they are arranged in alphabetical order and two different substituents are separated by hyphen (-) along with their position.
  • Name and positions of substituents are separated by a hyphen (-).
IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (5)
IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (6)
IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (7)

5. Complex alkyl substituent rule

If the alkyl substituent is further branched then it is named as substituent alkyl group. In this case, the alkyl group is separately numbered in such a way that the carbon atom that is directly attached to the parent chain is given the number 1 and the name is enclosed in the bracket.

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (8)

6. Multiple functional group rule

When a parent chain contains two or more functional groups, only one functional group is regarded as the principal functional group, and other functional groups are considered prefixes and written in front of word roots in alphabetical order along with their position. In this case, IUPAC naming takes place on the basis of the principal functional group. That is, the numbering of carbon atoms is done from that end which gives a lower number to the principal functional group.

Priority order of functional groups in IUPAC nomenclature

The following priority order of the functional group is used for selecting the principal functional group.

Carboxylic acid > Sulphonic acid > Acid anhydrides > Esters > Acid halides > Amides > Cyanide (Nitrile) > Aldehydes > Thio aldehydes > Ketones > Thio ketones > Alcohol > Thio alcohol > Amines

If the functional group-containing carbon atoms like -COOH, -CHO, -COOR, -COCl, -CN, etc. are present in the parent chain, then the carbon atom of the functional group gets always number 1 during the numbering of carbon in the parent chain.

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (9)
IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (10)
IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (11)
IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (12)

What is the IUPAC name for the following compound?

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (14)

Answer:

  1. 2-Chloro-4,4-dimethylhexane
  2. 3-Methyl but-1-ene
  3. 2-Methyl but-1-ene
  4. 3-(n-Propyl) hex-1-ene

Give IUPAC name for the following compound

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (15)

Answer:

A) 4-Methyl hex-2-yne

B) 5,7-Dimethyl deca-18-diene

C) 2-Methyl-1-phenyl propanamine

D) 4-Bromo-2-chloro-3-methyl hexane

Give the IUPAC name for the following compounds

IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (16)

Answer:

  1. Methanoic propanoic anhydride
  2. 2-Ethyl-4-formyl butanoic acid
  3. 2-Oxo propanal
  4. 2-Amino-2-ethoxy-4-methyl hexanol

FAQs/MCQs:

What is the full form of IUPAC?

The full form of IUPAC is the International Union of Pure and Applied Chemistry.

Write the priority order of functional groups in multifunctional organic compounds.

Carboxylic acid > Sulphonic acid > Acid anhydrides > Esters > Acid halides > Amides > Cyanide (Nitrile) > Aldehydes > Thio aldehydes > Ketones > Thio ketones > Alcohol > Thio alcohol > Amines

What is the prefix of thioalcohol?

The prefix of thioalcohol is mercapto.

What are the suffix and prefix of ester?

The suffix and prefix of ester are -oate and carbalkoxy- respectively.

Published by: Siddha Raj Upadhyaya (Gurudev)

Naming of organic compounds video

References:

  • A.M. Patterson and C.E. Curran, A system of organic nomenclature,J. Am. Chem. Soc.39, 1623-1638 (1917).
  • A Guide to IUPAC Nomenclature of Organic Compounds,Recommendations 1993, Blackwell Scientific Publications, 1993.
  • IUPAC Nomenclature of Organic Chemistry, Sections A and B, 1st edition, 1958; 2nd edition, 1966; 3rd edition (combined with section C), 1971;4th edition(combined with sections C, D, E, F and H), 1979.

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IUPAC nomenclature of organic compounds: 6 Rules and examples - Chemistry Notes (2024)

FAQs

What is the 6th rule of IUPAC nomenclature? ›

Rule 6 :- A cyclic hydrocarbon has a prefix cyclo before the name. Note : The IUPAC nomenclature is needed because earlier every chemist gave its own new name to the molecule it discovered.

What is the IUPAC nomenclature short notes? ›

IUPAC nomenclature is based on naming a molecule's longest chain of carbons connected by single bonds, whether in a continuous chain or in a ring. All deviations, either multiple bonds or atoms other than carbon and hydrogen, are indicated by prefixes or suffixes according to a specific set of priorities.

What are the rules for naming elements in IUPAC? ›

(i) The names should be short and obviously related to the atomic numbers of the elements. (ii) The names should end in 'ium' whether the element was expected to be a metal or otherwise. (iii) The symbols for the systematically named elements should consist of three letters.

What is 6 in IUPAC name? ›

Number of CarbonsName
5pentane
6hexane
7heptane
8octane
8 more rows

What is the IUPAC nomenclature of organic compounds? ›

In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book).

What is an example of Iupac name in organic chemistry? ›

In this nomenclature system, organic compounds are named with the use of functional groups as the prefix or suffix to the parent compounds name. Hydrides that belong to groups 13 to 17 of the modern periodic table are named with the suffix 'ane'. Examples of this include Borane, Phosphane, and oxidane, etc.

How are Iupac names written? ›

In summary, the name of the compound is written out with the substituents in alphabetical order followed by the base name (derived from the number of carbons in the parent chain). Commas are used between numbers and dashes are used between letters and numbers. There are no spaces in the name.

What are the rules of nomenclature? ›

The universal rules of nomenclature are as follows:
  • Biological names are in Latin and are written in italics.
  • The first word in the name indicates the genus, while the second word denotes its specific epithet.
  • When the name is handwritten, both the words are separately underlined.
Jul 3, 2022

Why is IUPAC nomenclature important? ›

Answer and Explanation: IUPAC nomenclature is important because it creates a standardized way to name chemical compounds.

How many types of IUPAC nomenclature are there? ›

There are three methods of nomenclature – Composition, Substitute, Additive nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) designed and developed the nomenclature that is most often used worldwide.

What is the full meaning of IUPAC? ›

The International Union of Pure and Applied Chemistry (IUPAC) is the international body that represents chemistry and related sciences and technologies.

What is the priority order of IUPAC nomenclature? ›

Solution: The priority of functional groups in IUPAC nomenclature is -COOH > -SO3H > -COOR > -COCl > -CONH₂ > -CN > HC=O > -CO > -OH > -NH₂ > C=C > C-C.

What is the parent or stem of a compound with 6 carbons? ›

Therefore, the Name of the stem (or word root) of a hydrocarbon containing six Carbon atoms is 'Hex'.

What is the full form of IUPAC rule? ›

International Union of Pure and Applied Chemistry.

What is the IUPAC nomenclature structure? ›

In general, an IUPAC name will have three essential features: A root or base indicating a major chain or ring of carbon atoms found in the molecular structure. A suffix or other element(s) designating functional groups that may be present in the compound.

References

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