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  2. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven. Where there is no confusion, some traditional names are also acceptable. Whatever method is used, all polymer names have the prefix poly, followed by enclosing marks around the rest of the name. The marks are used in the order: {[( )]}.

  3. Monomer - Wikipedia

    en.wikipedia.org/wiki/Monomer

    The polymerization of one kind of monomer gives a homopolymer. Many polymers are copolymers, meaning that they are derived from two different monomers. In the case of condensation polymerizations, the ratio of comonomers is usually 1:1. For example, the formation of many nylons requires equal amounts of a dicarboxylic acid and diamine. In the ...

  4. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    Another nomenclature uses the systematic name of the molecular graph, a ' D-' or ' L-' prefix to indicate the position of the last chiral hydroxyl on the Fischer diagram (as above), and another italic prefix to indicate the positions of the remaining hydroxyls relative to the first one, read from bottom to top in the diagram, skipping the keto ...

  5. Protein structure - Wikipedia

    en.wikipedia.org/wiki/Protein_structure

    Protein structure is the three-dimensional arrangement of atoms in an amino acid-chain molecule. Proteins are polymers – specifically polypeptides – formed from sequences of amino acids, which are the monomers of the polymer. A single amino acid monomer may also be called a residue, which indicates a

  6. Ideal chain - Wikipedia

    en.wikipedia.org/wiki/Ideal_chain

    While the elementary model described above is totally unadapted to the description of real-world polymers at the microscopic scale, it does show some relevance at the macroscopic scale in the case of a polymer in solution whose monomers form an ideal mix with the solvent (in which case, the interactions between monomer and monomer, solvent molecule and solvent molecule, and between monomer and ...

  7. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    Other monomer units, such as formaldehyde hydrates or simple aldehydes, are able to polymerize themselves at quite low temperatures (ca. −80 °C) to form trimers; [3] molecules consisting of 3 monomer units, which can cyclize to form ring cyclic structures, or undergo further reactions to form tetramers, [3] or 4 monomer-unit compounds.

  8. Dimerization - Wikipedia

    en.wikipedia.org/wiki/Dimerization

    Molecular dimers are often formed by the reaction of two identical compounds e.g.: 2A → A−A. In this example, monomer "A" is said to dimerize to give the dimer "A−A". Dicyclopentadiene is an asymmetrical dimer of two cyclopentadiene molecules that have reacted in a Diels-Alder reaction to give the product. Upon heating, it "cracks ...

  9. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    For example, the aldohexose glucose may form a hemiacetal linkage between the aldehyde group on carbon 1 and the hydroxyl on carbon 4, yielding a molecule with a 5-membered ring, called glucofuranose. The same reaction can take place between carbons 1 and 5 to form a molecule with a 6-membered ring, called glucopyranose.

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