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  2. End group - Wikipedia

    en.wikipedia.org/wiki/End_group

    The advantage of NMR for end groups is that it allows for not only the identification of the end group units, but also allows for the quantification of the number-average length of the polymer. [7] End-group analysis with NMR requires that the polymer be soluble in organic or aqueous solvents. Additionally, the signal on the end-group must be ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    If the alkyl group is not attached at the end of the chain, the bond position to the ester group is suffixed before "-yl": CH 3 CH 2 CH(CH 3)OOCCH 2 CH 3 may be called butan-2-yl propanoate or butan-2-yl propionate. [citation needed]. The prefix form is "oxycarbonyl-" with the (R') group preceding.

  4. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    The bonds between atoms can be omitted, but dashes should be drawn for chain-ends. The seniority of the subunits does not need to be followed. For single-strand (co)polymers, a dash is drawn through the enclosing marks, e.g., poly[oxy(ethane-1,2-diyl)] shown below left.

  5. International Union of Pure and Applied Chemistry - Wikipedia

    en.wikipedia.org/wiki/International_Union_of...

    IUPAC organic nomenclature has three basic parts: the substituents, carbon chain length, and chemical affix. [14] The substituents are any functional groups attached to the main carbon chain. The main carbon chain is the longest possible continuous chain. The chemical affix denotes what type of molecule it is.

  6. Bond length - Wikipedia

    en.wikipedia.org/wiki/Bond_length

    It is generally considered the average length for a carbon–carbon single bond, but is also the largest bond length that exists for ordinary carbon covalent bonds. Since one atomic unit of length (i.e., a Bohr radius) is 52.9177 pm, the C–C bond length is 2.91 atomic units, or approximately three Bohr radii long.

  7. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    This naming method generally follows established IUPAC organic nomenclature. Hydrides of the main group elements (groups 13–17) are given the base name ending with -ane, e.g. borane (B H 3), oxidane (H 2 O), phosphane (P H 3) (Although the name phosphine is also in common use, it is not recommended by

  8. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC states that, "As one of its major activities, IUPAC develops Recommendations to establish unambiguous, uniform, and consistent nomenclature and terminology for specific scientific fields, usually presented as: glossaries of terms for specific chemical disciplines; definitions of terms relating to a group of properties; nomenclature of chemical compounds and their classes; terminology ...

  9. Commission on Isotopic Abundances and Atomic Weights

    en.wikipedia.org/wiki/Commission_on_Isotopic...

    By the end of the 19th century, two scales gained popular support: H=1 and O=16. This situation was undesired in science and in October 1899, the inaugural task of the International Commission on Atomic Weights was to decide on the international scale and the oxygen scale became the international standard. [ 12 ]