{"id":1273,"date":"2018-03-21T14:46:40","date_gmt":"2018-03-21T14:46:40","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/end-of-chapter-material-4\/"},"modified":"2018-10-30T15:30:37","modified_gmt":"2018-10-30T15:30:37","slug":"end-of-chapter-material-4","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/end-of-chapter-material-4\/","title":{"raw":"13.9 End-of-Chapter Material","rendered":"13.9 End-of-Chapter Material"},"content":{"raw":"
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Chapter Summary<\/h3>\r\n

To ensure that you understand the material in this chapter, you should review the meanings of the bold terms in the following summary and ask yourself how they relate to the topics in the chapter.<\/em><\/p>\r\n

Any hydrocarbon containing either a double or triple bond is an unsaturated hydrocarbon<\/strong>. Alkenes<\/strong> have a carbon-to-carbon double bond. The general formula for alkenes with one double bond is Cn<\/em><\/sub>H2<\/sub>n<\/em><\/sub>. Alkenes can be straight chain, branched chain, or cyclic. Simple alkenes often have common names, but all alkenes can be named by the system of the International Union of Pure and Applied Chemistry.<\/p>\r\n

Cis-trans isomers (or geometric isomers)<\/strong> are characterized by molecules that differ only in their configuration around a rigid part of the structure, such as a carbon\u2013to-carbon double bond or a ring. The molecule having two identical atoms or groups on the same side is the cis isomer<\/strong>; the one having the two like groups on opposite sides is the trans isomer<\/strong>.<\/p>\r\n

The physical properties of alkenes are quite similar to those of alkanes. Like other hydrocarbons, alkenes are insoluble in water but soluble in organic solvents.<\/p>\r\n

More reactive than alkanes, alkenes undergo addition reactions<\/strong> across the double bond:<\/p>\r\n\r\n

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    Addition of hydrogen (hydrogenation<\/strong>):<\/p>\r\nCH2<\/sub>=CH2<\/sub> + H2<\/sub> \u2192 CH3<\/sub>CH3<\/sub><\/span><\/span><\/li>\r\n \t

  • \r\n

    Addition of halogen (halogenation<\/strong>):<\/p>\r\nCH2<\/sub>=CH2<\/sub> + X2<\/sub> \u2192 XCH2<\/sub>CH2<\/sub>X<\/span><\/span>\r\n

    where X = F, Cl, Br, or I.<\/p>\r\n<\/li>\r\n \t

  • \r\n

    Addition of water (hydration<\/strong>):<\/p>\r\nCH2<\/sub>=CH2<\/sub> + HOH \u2192 HCH2<\/sub>CH2<\/sub>OH<\/span><\/span><\/li>\r\n<\/ul>\r\n

    Alkenes also undergo addition polymerization<\/strong>, molecules joining together to form long-chain molecules.<\/p>\r\n\u2026CH2<\/sub>=CH2<\/sub> + CH2<\/sub>=CH2<\/sub> + CH2<\/sub>=CH2<\/sub> +\u2026\u2192\u2026CH2<\/sub>CH2<\/sub>\u2013CH2<\/sub>CH2<\/sub>\u2013CH2<\/sub>CH2<\/sub>\u2013\u2026<\/span><\/span>\r\n

    The reactant units are monomers<\/strong>, and the product is a polymer<\/strong>.<\/p>\r\n

    Alkynes<\/strong> have a carbon-to-carbon triple bond. The general formula for alkynes is Cn<\/em><\/sub>H2<\/sub>n<\/em><\/sub> \u2212 2<\/sub>. The properties of alkynes are quite similar to those of alkenes. They are named much like alkenes but with the ending -yne<\/em>.<\/p>\r\n

    The cyclic hydrocarbon benzene<\/em> (C6<\/sub>H6<\/sub>) has a ring of carbon atoms. The molecule seems to be unsaturated, but it does not undergo the typical reactions expected of alkenes. The electrons that might be fixed in three double bonds are instead delocalized<\/em> over all six carbon atoms.<\/p>\r\n

    A hydrocarbon containing one or more benzene rings is an aromatic hydrocarbon.\u00a0<\/strong>(Note: Not all aromatic substances contain benzene rings, but broader definition of aromaticity will not be considered in this text.)\u00a0 One or more of the hydrogen atoms on a benzene ring can be replaced by other atoms. When two hydrogen atoms are replaced, the product name is based on the relative position of the replacement atoms (or atom groups). A 1,2-disubstituted benzene is designated as an ortho<\/em> (o<\/em>-) isomer; 1,3-, a meta<\/em> (m<\/em>-) isomer; and 1,4-, a para<\/em> (p<\/em>-) isomer. The IUPAC system uses only the numbers and not the ortho, meta, and para desriptors.\u00a0 An aromatic group as a substituent is called an aryl<\/strong> group.<\/p>\r\n

    A polycyclic aromatic hydrocarbon (PAH)<\/strong> has fused benzene rings sharing a common side.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n

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    Additional Exercises<\/h3>\r\n
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    1. \r\n
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      Classify each compound as saturated or unsaturated.<\/p>\r\n\r\n

        \r\n \t
      1. \r\n
        \"image\"<\/div><\/li>\r\n \t
      2. CH3<\/sub>C\u2261CCH3<\/sub><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t
      3. \r\n
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        Classify each compound as saturated or unsaturated.<\/p>\r\n\r\n

          \r\n \t
        1. \r\n
          \"image\"<\/div><\/li>\r\n \t
        2. \r\n
          \"image\"<\/div><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t
        3. \r\n
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          Give the molecular formula for each compound. (Note that the CH3<\/sub> in the ring on b should be CH2<\/sub>. MK)<\/p>\r\n\r\n

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          1. \r\n
            \"image\"<\/div><\/li>\r\n \t
          2. \r\n
            \"image\"<\/div><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t
          3. \r\n
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            When three isomeric pentenes\u2014X, Y, and Z\u2014are hydrogenated, all three form 2-methylbutane. The addition of Cl2<\/sub> to Y gives 1,2-dichloro-3-methylbutane, and the addition of Cl2<\/sub> to Z gives 1,2-dichloro-2-methylbutane. Draw the original structures for X, Y, and Z.<\/p>\r\n\r\n<\/div><\/li>\r\n \t

          4. \r\n
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            Pentane and 1-pentene are both colorless, low-boiling liquids. Describe a simple test that distinguishes the two compounds. Indicate what you would observe.<\/p>\r\n\r\n<\/div><\/li>\r\n \t

          5. \r\n
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            Draw and name all the alkene cis-trans isomers corresponding to the molecular formula C5<\/sub>H10<\/sub>. (Hint: there are only two.)<\/p>\r\n\r\n<\/div><\/li>\r\n \t

          6. \r\n
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            The complete combustion of benzene forms carbon dioxide and water:<\/p>\r\nC6<\/sub>H6<\/sub> + O2<\/sub> \u2192 CO2<\/sub> + H2<\/sub>O<\/span><\/span>\r\n

            Balance the equation. What mass, in grams, of carbon dioxide is formed by the complete combustion of 39.0 g of benzene?<\/p>\r\n\r\n<\/div><\/li>\r\n \t

          7. \r\n
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            Describe a physiological effect of some PAHs.<\/p>\r\n\r\n<\/div><\/li>\r\n \t

          8. \r\n
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            What are some of the hazards associated with the use of benzene?<\/p>\r\n\r\n<\/div><\/li>\r\n \t

          9. \r\n
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            What is wrong with each name? Draw the structure and give the correct name for each compound.<\/p>\r\n\r\n

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            1. 2-methyl-4-heptene<\/li>\r\n \t
            2. 2-ethyl-2-hexene<\/li>\r\n \t
            3. 2,2-dimethyl-3-pentene<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t
            4. \r\n
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              What is wrong with each name?<\/p>\r\n\r\n

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              1. 2-bromobenzene<\/li>\r\n \t
              2. 3,3-dichlorotoluene<\/li>\r\n \t
              3. 1,4-dimethylnitrobenzene<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t
              4. \r\n
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                Following are line-angle formulas for three compounds. Draw the structure and give the name for each.<\/p>\r\n\r\n

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                1. \r\n
                  \"image\"<\/div><\/li>\r\n \t
                2. \r\n
                  \"image\"<\/div><\/li>\r\n \t
                3. \r\n
                  \"image\"\r\n

                  <\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n

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                  Answers<\/h3>\r\n<\/div>\r\n
                  \r\n\r\n[reveal-answer q=\"521124\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"521124\"]\r\n\r\n1. a. unsaturated\r\n\r\nb. unsaturated\r\n
                  <\/div>\r\n
                  \r\n\r\n3. a. C6<\/sub>H10<\/sub>\r\n\r\nb. C4<\/sub>H8<\/sub>\r\n\r\n<\/div>\r\n
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                  5. Add bromine solution (reddish-brown) to each. Pentane will not react, and the reddish-brown color persists; 1-pentene will react, leaving a colorless solution.<\/p>\r\n\r\n<\/div>\r\n

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                  7. 2C6<\/sub>H6<\/sub> + 15O2<\/sub> \u2192 12CO2<\/sub> + 6H2<\/sub>O; 132 g<\/p>\r\n\r\n<\/div>\r\n

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                  9. carcinogenic, flammable<\/p>\r\n\r\n<\/div>\r\n

                  <\/div>\r\n
                  \r\n\r\n11. a. number not needed\r\n\r\nb. can\u2019t have two groups on one carbon atom on a benzene ring\r\n\r\nc. can\u2019t have a substituent on the same carbon atom as the nitro group\r\n\r\n<\/div>\r\n
                  <\/div>\r\n
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                  <\/div>\r\n<\/div>\r\n
                  [\/hidden-answer]<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n
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                  <\/div>\r\n<\/div>","rendered":"
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                  Chapter Summary<\/h3>\n

                  To ensure that you understand the material in this chapter, you should review the meanings of the bold terms in the following summary and ask yourself how they relate to the topics in the chapter.<\/em><\/p>\n

                  Any hydrocarbon containing either a double or triple bond is an unsaturated hydrocarbon<\/strong>. Alkenes<\/strong> have a carbon-to-carbon double bond. The general formula for alkenes with one double bond is Cn<\/em><\/sub>H2<\/sub>n<\/em><\/sub>. Alkenes can be straight chain, branched chain, or cyclic. Simple alkenes often have common names, but all alkenes can be named by the system of the International Union of Pure and Applied Chemistry.<\/p>\n

                  Cis-trans isomers (or geometric isomers)<\/strong> are characterized by molecules that differ only in their configuration around a rigid part of the structure, such as a carbon\u2013to-carbon double bond or a ring. The molecule having two identical atoms or groups on the same side is the cis isomer<\/strong>; the one having the two like groups on opposite sides is the trans isomer<\/strong>.<\/p>\n

                  The physical properties of alkenes are quite similar to those of alkanes. Like other hydrocarbons, alkenes are insoluble in water but soluble in organic solvents.<\/p>\n

                  More reactive than alkanes, alkenes undergo addition reactions<\/strong> across the double bond:<\/p>\n