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Parallel Exercises A
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Note:  You will need to refer to Table 12.5 below to complete some of the following exercises.

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  1. Draw the structural formulas for (a) n-pentane, and (b) an isomer of pentane with the maximum possible branching. (c) Give the IUPAC name of this isomer.
    Click here to see the answer (13.0K)

  2. Write structural formulas for all the hexane isomers you can identify. Write the IUPAC name for each isomer.
    Click here to see the answer (40.0K)

  3. Write structural formulas for
    a. 3,3,4-trimethyloctane.
    b. 2-methyl-1-pentene.
    c. 5,5-dimethyl-3-heptyne.
    Click here to see the answer (13.0K)

  4. Write the IUPAC name for each of the following.
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    <a onClick="window.open('/olcweb/cgi/pluginpop.cgi?it=jpg::::/sites/dl/free/0072509783/121104/chap12parexa_q4b.jpg','popWin', 'width=287,height=290,resizable,scrollbars');" href="#"><img valign="absmiddle" height="16" width="16" border="0" src="/olcweb/styles/shared/linkicons/image.gif"> (5.0K)</a>
    Click here to see the answer (4.0K)

  5. Which would have the higher octane rating, 2,2,3-trimethylbutane or 2,2-dimethylpentane? Explain with an illustration.
    Click here to see the answer (13.0K)

  6. Use the information in Table 12.5 to classify each of the following as an alcohol, ether, organic acid, ester, or amide.
    <a onClick="window.open('/olcweb/cgi/pluginpop.cgi?it=jpg::::/sites/dl/free/0072509783/121104/chap12parexa_q6.jpg','popWin', 'width=347,height=537,resizable,scrollbars');" href="#"><img valign="absmiddle" height="16" width="16" border="0" src="/olcweb/styles/shared/linkicons/image.gif"> (15.0K)</a>
    Click here to see the answer (3.0K)








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