enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Propyl group - Wikipedia

    en.wikipedia.org/wiki/Propyl_group

    From left to right: the two isomeric groups propyl and 1-methylethyl (iPr or isopropyl), and the non-isomeric cyclopropyl group. In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH 2 CH 2 CH 3 for the linear form.

  3. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    The subunits that make up each of these structures are identified, i.e., the largest divalent groups that can be named using IUPAC nomenclature of organic chemistry. In the example, the two-carbon ethylidene unit is longer than two separate one-carbon methanediyl units. Figure 1. The order of subunit precedence.

  4. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H 14: n-hexane: dipropyl; Gettysolve-B; hexyl hydride; Skellysolve B 7 9 11 C 7 H 16: n-heptane: dipropyl methane; Gettysolve-C; heptyl hydride; Skellysolve C 8 18 24 C 8 H 18: n-octane ...

  5. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    6.1 Dimethyl+Propyl. 6.2 Diethyl+Methyl. 6.3 Ethyl+Trimethyl. 6.4 Pentamethyl. 7 References. Toggle the table of contents. List of isomers of decane. 7 languages ...

  6. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    For example, there are three distinct compounds with the molecular formula : . Structural isomers of C 3 H 8 O: I 1-propanol, II 2-propanol, III ethyl-methyl-ether.. The first two isomers shown of are propanols, that is, alcohols derived from propane.

  7. Metamerism (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Metamerism_(Chemistry)

    In chemistry, metamerism is used to define the isomeric relationship between compounds with the same polyvalent, heteroatomic, functional group but differ in the main carbon chain or any of the side chains. It has rather been an obsolete term for isomerism, which has not been recognised by IUPAC in its publications. [1]

  8. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An example of an ester formation is the substitution reaction between a carboxylic acid (R−C(=O)−OH) and an alcohol (R'OH), forming an ester (R−C(=O)−O−R'), where R and R′ are organyl groups, or H in the case of esters of formic acid.

  9. Isopropyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_alcohol

    Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable, organic compound with a pungent alcoholic odor. [9]Isopropyl alcohol, an organic polar molecule, is miscible in water, ethanol, and chloroform, demonstrating its ability to dissolve a wide range of substances including ethyl cellulose, polyvinyl butyral, oils, alkaloids, and natural ...