enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. List of isomers of tridecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_tridecane

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  3. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    This compound is known as 2,3,3-trimethylpentane. Here three identical alkyl groups attached to carbon atoms 2, 3, and 3. Here three identical alkyl groups attached to carbon atoms 2, 3, and 3. The numbers are included in the name to avoid ambiguity about the position of the groups, and "tri" indicates that there are three identical methyl groups.

  4. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  5. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Number of isomers [3] [4] Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride ...

  6. 3-Ethylpentane - Wikipedia

    en.wikipedia.org/wiki/3-ethylpentane

    3-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]

  7. Hagemann's ester - Wikipedia

    en.wikipedia.org/wiki/Hagemann's_ester

    Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many natural products including sterols , trisporic acids , and terpenoids .

  8. Peterson olefination - Wikipedia

    en.wikipedia.org/wiki/Peterson_olefination

    The Peterson olefination (also called the Peterson reaction) is the chemical reaction of α-silyl carbanions (1 in diagram below) with ketones (or aldehydes) to form a β-hydroxysilane (2) which eliminates to form alkenes (3).

  9. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    2-ethyl-3- methylbutanoic acid CH 3 CH(CH 3)CH(C 2 H 5)COOH C8. IUPAC name: Common name: ... CH 3 (CH 2) 10 COOH benzene-1,2,3,4,5,6-hexacarboxylic acid: mellitic acid