Ask Question
24 February, 08:51

A certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis gave CH3 (CH2) 4CO2H and HO2CCH2CH2CO2H as the only products. Draw a reasonable structure for this hydrocarbon. Click the draw structure" button to launch the drawing utility."

+3
Answers (1)
  1. 24 February, 09:04
    0
    the compound is hexadeca-6,10-diyne.

    Explanation:

    As given that the compound has two triple bonds and it is giving carboxylic acids on ozonolyis so this is an oxidative ozonolysis.

    We are getting only two kinds of products, it means the triple bonds are located at symmetrical position.

    The middle carbon chain must have four carbons and the side chains must have six carbons each,

    The structure of hydrocarbon is shown in figure.
Know the Answer?
Not Sure About the Answer?
Find an answer to your question ✅ “A certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis gave CH3 (CH2) 4CO2H and HO2CCH2CH2CO2H ...” in 📘 Chemistry if you're in doubt about the correctness of the answers or there's no answer, then try to use the smart search and find answers to the similar questions.
Search for Other Answers