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Iupac Nomenclature Rules 1

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IUPAC NOMENCLATURE: For Organic Compounds

3 parts: PREFIX-ROOT-SUFFIX
1. ROOT (or BASE) – indicates a major chain or ring of carbon atoms serving as the basic
(parent) skeleton.
2. SUFFIX (or other element) – designates the most important functional group in the molecule.
3. A SERIES OF PREFIXES – describe the modification mode in the basic skeleton to form the
structure in question (branches or substituents)

RULES:
1. Find the longest continuous carbon chain in the molecule and name as a derivative of the
normal alkane having the same number of carbon.
C1 meth C6 hex C11 undec
C2 eth C7 hept C12 dodec
C3 prop C8 oct C13 tridec
C4 but C9 non C14 tetradec
C5 pent C10 dec C15 pentadec
2. Number that chain starting from the end that gives the smaller set of numbers.
- For cyclic structures having only one substituent on the ring, there is no need to number
the atoms of ring.
- For 2 or more substituents on the ring, a numbering system must be used to locate the groups.
e.g. bromocyclopentane 1,2-dichlorocyclohexane
3. List the alkyl groups or substituents attached to the main chain (in alphabetical order) as a
series of prefixes to the root name. If two or more identical side chains are present use the
Greek prefixes di-, tri-, tetra-, penta- and so forth.
4. Write the name as a single word, using hyphens to separate the various prefixes and commas to
separate numbers.
5. If a choice of 2 basic chains of equal length must be made, choose that one which gives a
maximum number of simple side chains.
Group Nomenclature: Prefixes and Suffixes
Functional Group Prefix Suffix
A. Groups indicated by suffix only:
Alkanes (C C) NONE - -ane
Alkenes C=C - -ene
Alkynes C C - -yne
B. Groups indicated by prefix or suffix:
COOH or CO2H
Carboxylic acids carboxy- -oic acid
O

C
. OH
O

C
Aldehydes CHO or . H oxo- -al
O

C
Ketones . . oxo- -one
Alcohols OH hydroxy- -ol
Amines NH2 amino- -amine
C. Groups indicated by prefix only:
Halogenated compounds F fluoro- -
Cl chloro- -
Br bromo- -
I iodo- -
Nitrated compounds NO2 nitro- -
Alkylated compounds R alkyl- -
Ethers OR alkoxy- -

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