Anmelden

In the late 19th-century, the number of new chemical compounds discovered increased tremendously. Hence, the necessity arose to develop a naming system for the systematic nomenclature of these newly discovered compounds. IUPAC (International Union for Pure and Applied Chemistry), established in 1919, sets rules for the nomenclature.

The alkane nomenclature considers the length of the carbon chain, the number, and the location of the substituent to arrive at its systematic name. The IUPAC nomenclature is done stepwise, and it is universally acceptable. The first step is to determine and name the longest carbon chain, also known as the parent chain. For example, an alkane having the longest carbon chain of five carbon atoms gets the parent name pentane.

The second step is to identify and name the substituents. The name of the substituent, known as a prefix, is positioned before the parent name. For example, a pentane chain having a methyl substituent gets the name methylpentane. The third step is to determine the location of the substituent by numbering the longest carbon chain. The numbering is done in such a way that the carbon on which the substituent is situated gets the lowest number. Thus, the methyl group positioned on the second carbon will obtain the name 2-methyl pentaneand not 4-methyl pentane. If more than one identical or non-identical substituents are present, additional IUPAC rules apply.

Tags

NomenclatureAlkanesChemical CompoundsSystematic NomenclatureIUPACCarbon ChainSubstituentParent ChainPrefixMethyl GroupNumberingIdentical SubstituentsNon identical Substituents

Aus Kapitel 3:

article

Now Playing

3.3 : Nomenclature of Alkanes

Alkane und Cycloalkane

20.5K Ansichten

article

3.1 : Struktur der Alkane

Alkane und Cycloalkane

26.1K Ansichten

article

3.2 : Konstitutionelle Isomere von Alkanen

Alkane und Cycloalkane

17.3K Ansichten

article

3.4 : Physikalische Eigenschaften von Alkanen

Alkane und Cycloalkane

10.5K Ansichten

article

3.5 : Newman-Projektionen

Alkane und Cycloalkane

15.7K Ansichten

article

3.6 : Konformationen von Ethan und Propan

Alkane und Cycloalkane

13.3K Ansichten

article

3.7 : Konformationen von Butan

Alkane und Cycloalkane

13.4K Ansichten

article

3.8 : Cycloalkane

Alkane und Cycloalkane

11.7K Ansichten

article

3.9 : Konformationen von Cycloalkanen

Alkane und Cycloalkane

11.3K Ansichten

article

3.10 : Konformationen von Cyclohexan

Alkane und Cycloalkane

11.6K Ansichten

article

3.11 : Stuhlkonformation von Cyclohexan

Alkane und Cycloalkane

13.9K Ansichten

article

3.12 : Stabilität von substituierten Cyclohexanen

Alkane und Cycloalkane

12.1K Ansichten

article

3.13 : Disubstituierte Cyclohexane: cis-trans-Isomerie

Alkane und Cycloalkane

11.4K Ansichten

article

3.14 : Verbrennungsenergie: Ein Maß für die Stabilität von Alkanen und Cycloalkanen

Alkane und Cycloalkane

6.1K Ansichten

JoVE Logo

Datenschutz

Nutzungsbedingungen

Richtlinien

Forschung

Lehre

ÜBER JoVE

Copyright © 2025 MyJoVE Corporation. Alle Rechte vorbehalten