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. Quizalofop - Wikipedia

    en.wikipedia.org/wiki/Quizalofop

    It may be shortened to QPE, from Quizalofop-P-Ethyl. [3] It is a Group 1 / A / A herbicide, used in Australia, [4] Morocco and Europe. [1] Affected weeds show symptoms after 7 to 10 days, the base and inter-veins become yellow; new growth joints are weak. After 16 days, tips become yellow or red and the plant falls apart. [4]

  4. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    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. If one of the methyl groups attached to the third carbon atom were instead an ethyl group, then the name would be 3-ethyl-2,3-dimethylpentane.

  5. 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]

  6. List of isomers of nonane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_nonane

    5.3 Diethyl. Toggle the table of contents. ... 3-Ethyl-3-methylhexane; 3-Ethyl-4-methylhexane; Pentane. Isomers where pentane is the longest chain Tetramethyl

  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. Heptanone - Wikipedia

    en.wikipedia.org/wiki/Heptanone

    Heptanone may refer to the following ketones with seven carbon atoms the formula C 7 H 14 O: . 2-Heptanone (Methyl amyl ketone) . 5-Methyl-2-hexanone (Methyl isoamyl ketone); 4-Methyl-2-hexanone (Methyl 2-methylbutyl ketone)