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JoVE Core
Organic Chemistry
Characteristics and Nomenclature of Homopolymers
Characteristics and Nomenclature of Homopolymers
JoVE Core
Organic Chemistry
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JoVE Core Organic Chemistry
Characteristics and Nomenclature of Homopolymers

21.1: Characteristics and Nomenclature of Homopolymers

3,683 Views
01:00 min
April 30, 2023

Overview

Polymers that are made up of identical monomer units are called homopolymers. Only one repeating unit is involved in the construction of the homopolymer structure. For example, as depicted in Figure 1, polypropylene is a homopolymer constituted of propylene monomers. Here, the only repeating unit in the polymer chain is propylene.

Polymerization process, chemical equation, diagram of ethylene to polyethylene conversion.

Figure 1: Propylene homopolymerization to polypropylene.

The chemical name of a homopolymer is generated by using the name of its monomer with a prefix ‘poly’. For example, the homopolymer synthesized from propylene is known as polypropylene. At times, the monomer name is enclosed with a parenthesis distinct from the prefix poly, such as when multiple components or substituents are present in the monomer. Figure 2 illustrates one such example with the homopolymer obtained from tetrafluoroethylene. Another popular example is poly(vinyl chloride).

Polymerization diagram, CF2=CF2 to (C2F4)n, showing molecular structure transformation process.

Figure 2: Tetrafluoroethylene homopolymerization to poly(tetrafluoroethylene).

The other components of the structure like the notations of unsaturation, stereochemistry around the unsaturation, and the position of functional groups in the monomer are often placed in front of the prefix poly in the polymer’s nomenclature. This is illustrated in Figure 3, which shows the polymerization of chloroprene (2-chloro-1,3-butadiene) to poly(chloroprene), or neoprene (synthetic rubber).

Polymerization process diagram, showing monomer to polymer conversion, vinyl chloride structure.

Figure 3: Polymerization of chloroprene (2-chloro-1,3-butadiene) to trans-1,4-poly(chloroprene) (sometimes trans-2-chloro-1,3-polybutadiene).

Formal scientific usage may employ a fully structure-based convention wherein the entire structural repeating unit is enclosed in parentheses or brackets after ‘poly’, as in poly(2-chlorobuta-1,3-diene) or poly[(Z)-1-chlorobut-2-ene-1,4-diyl].

However, most often, polymers are known by their trade name rather than the chemical name. This is evidenced in the case of the lesser-known chemical names of well-known polymers based on compositions like poly(tetrafluoroethylene) and poly(paraphenylene terephthalamide).

Transcript

Homopolymers are constituted of identical monomers, and the resulting polymer chain contains a single type of repeating unit.

Note that the polymers are chemically represented by placing parentheses or brackets around the repeating unit in the polymer chain, with the degree of polymerization as a subscript to the right.

The common names for homopolymers attach the prefix 'poly' to the name of the monomer.

The monomer name may be put in parentheses, especially if its name has multiple components, such as two-word names or names with multiplicative prefixes of their own.

The notations indicating stereochemistry, locants, functional groups, or unsaturation in either the monomer or the repeating unit may be seen before the prefix 'poly'.

Often, the polymer is best known by its trade name, as in the case of polytetrafluoroethylene.

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HomopolymersMonomer UnitsPolypropylenePoly(tetrafluoroethylene)Poly(vinyl Chloride)ChloropreneNeoprenePolymerizationNomenclatureFunctional GroupsStereochemistryRepeating UnitChemical Name

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