{"id":1020,"date":"2018-03-20T16:53:58","date_gmt":"2018-03-20T16:53:58","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/?post_type=chapter&p=1020"},"modified":"2018-10-30T14:44:26","modified_gmt":"2018-10-30T14:44:26","slug":"12-5-iupac-nomenclature","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/12-5-iupac-nomenclature\/","title":{"raw":"12.5 IUPAC Nomenclature","rendered":"12.5 IUPAC Nomenclature"},"content":{"raw":"
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Learning Objective<\/h3>\r\n
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  1. Name alkanes by the IUPAC system and write formulas for alkanes given IUPAC names.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\nAs noted in <\/span>Table 12.2 \"The First 10 Straight-Chain Alkanes\"<\/a>, the number of isomers increases rapidly as the number of carbon atoms increases. There are 3 pentanes, 5 hexanes, 9 heptanes, and 18 octanes. It would be difficult to assign unique individual names that we could remember. A systematic way of naming hydrocarbons and other organic compounds has been devised by the International Union of Pure and Applied Chemistry (IUPAC). These rules, used worldwide, are known as the <\/span>IUPAC System of Nomenclature<\/span><\/strong><\/span>. (Some of the names we used earlier, such as isobutane, isopentane, and neopentane, do not follow these rules and are called <\/span>common names<\/em>.) A stem name (<\/span>Table 12.3 \"Stems That Indicate the Number of Carbon Atoms in Organic Molecules\"<\/a>) indicates the number of carbon atoms in the longest continuous chain (LCC). Atoms or groups attached to this carbon chain, called <\/span>substituents<\/em>, are then named, with their positions indicated by numbers. For now, we will consider only those substituents called alkyl groups.<\/span>\r\n\r\n<\/div>\r\n<\/div>\r\n
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    Table 12.3<\/span> Stems That Indicate the Number of Carbon Atoms in Organic Molecules<\/strong><\/h5>\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n
    Stem<\/th>\r\nNumber<\/th>\r\n<\/tr>\r\n<\/thead>\r\n
    meth-<\/td>\r\n1<\/td>\r\n<\/tr>\r\n
    eth-<\/td>\r\n2<\/td>\r\n<\/tr>\r\n
    prop-<\/td>\r\n3<\/td>\r\n<\/tr>\r\n
    but-<\/td>\r\n4<\/td>\r\n<\/tr>\r\n
    pent-<\/td>\r\n5<\/td>\r\n<\/tr>\r\n
    hex-<\/td>\r\n6<\/td>\r\n<\/tr>\r\n
    hept-<\/td>\r\n7<\/td>\r\n<\/tr>\r\n
    oct-<\/td>\r\n8<\/td>\r\n<\/tr>\r\n
    non-<\/td>\r\n9<\/td>\r\n<\/tr>\r\n
    dec-<\/td>\r\n10<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\r\n

    An alkyl group<\/span><\/strong><\/span>\u00a0is a group of atoms that results when one hydrogen atom is removed from an alkane. The group is named by replacing the -ane<\/em> suffix of the parent hydrocarbon with -yl<\/em>. For example, the CH3<\/sub> group derived from methane (CH4<\/sub>) results from subtracting one hydrogen atom and is called a methyl group<\/em>.<\/p>\r\n

    The alkyl groups we will use most frequently are listed in Table 12.4 \"Common Alkyl Groups\"<\/a>. Alkyl groups are not independent molecules; they are parts of molecules that we consider as a unit to name compounds systematically.<\/p>\r\n\r\n

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    Table 12.4<\/span> Common Alkyl Groups<\/strong><\/h5>\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n
    Parent Alkane<\/th>\r\nAlkyl Group<\/th>\r\nCondensed Structural Formula<\/th>\r\n<\/tr>\r\n<\/thead>\r\n
    methane<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		methyl<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		CH3<\/sub>\u2013<\/td>\r\n<\/tr>\r\n
    ethane<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		ethyl<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		CH3<\/sub>CH2<\/sub>\u2013<\/td>\r\n<\/tr>\r\n
    propane<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		propyl<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		CH3<\/sub>CH2<\/sub>CH2<\/sub>\u2013<\/td>\r\n<\/tr>\r\n
    <\/td>\r\n<\/td>\r\nisopropyl<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		(CH3<\/sub>)2<\/sub>CH\u2013<\/td>\r\n<\/tr>\r\n
    butane<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		butyl*<\/td>\r\n\r\n
    \"image\"<\/div><\/td>\r\n
    		CH3<\/sub>CH2<\/sub>CH2<\/sub>CH2<\/sub>\u2013<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n
    *There are four butyl groups, two derived from butane and two from isobutane. We will introduce the other three where appropriate.<\/th>\r\n<\/tr>\r\n<\/tfoot>\r\n<\/table>\r\n<\/div>\r\n

    Simplified IUPAC rules for naming alkanes are as follows (demonstrated in Example 12.1).<\/p>\r\n

    1. Name alkanes according to the longest continuous chain (LCC) of carbon atoms in the molecule rather than the total number of carbon atoms.<\/strong> This LCC, considered the parent chain, determines the base name, to which we add the suffix -ane<\/em> to indicate that the molecule is an alkane.<\/p>\r\n

    2. If the hydrocarbon is branched, number the carbon atoms of the LCC.<\/strong> Numbers are assigned in the direction that gives the lowest numbers to the carbon atoms with attached substituents. Hyphens are used to separate numbers from the names of substituents; commas separate numbers from each other. The LCC need not be written in a straight line; for example, the LCC in the following has five carbon atoms.<\/p>\r\n\r\n

    \"image\"<\/div>\r\n

    3. Place the names of the substituent groups in alphabetical order before the name of the parent compound.<\/strong> If the same alkyl group appears more than once, the numbers of all the carbon atoms to which it is attached are expressed. If the same group appears more than once on the same carbon atom, the number of that carbon atom is repeated as many times as the group appears. Moreover, the number of identical groups is indicated by the Greek prefixes di<\/em>-, tri<\/em>-, tetra<\/em>-, and so on. These prefixes are not<\/em> considered in determining the alphabetical order of the substituents. For example, ethyl is listed before dimethyl; the di- is simply ignored. The last alkyl group named is prefixed to the name of the parent alkane to form one word.<\/p>\r\n

    When these rules are followed, every unique compound receives its own exclusive name. The rules enable us to not only name a compound from a given structure but also draw a structure from a given name. The best way to learn how to use the IUPAC system is to put it to work, not just memorize the rules. It\u2019s easier than it looks.<\/p>\r\n\r\n

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    Example 1<\/h3>\r\n

    Name each compound.<\/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\"<\/div><\/li>\r\n<\/ol>\r\n

      Solution<\/p>\r\n\r\n

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      1. The LCC has five carbon atoms, and so the parent compound is pentane (rule 1). There is a methyl group (rule 2) attached to the second carbon atom of the pentane chain. The name is therefore 2-methylpentane.<\/li>\r\n \t
      2. The LCC has six carbon atoms, so the parent compound is hexane (rule 1). Methyl groups (rule 2) are attached to the second and fifth carbon atoms. The name is 2,5-dimethylhexane.<\/li>\r\n \t
      3. The LCC has eight carbon atoms, so the parent compound is octane (rule 1). There are methyl and ethyl groups (rule 2), both attached to the fourth carbon atom (counting from the right<\/em> gives this carbon atom a lower number; rule 3). The correct name is thus 4-ethyl-4-methyloctane.<\/li>\r\n<\/ol>\r\n<\/div>\r\n
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        Skill-Building Exercise<\/h3>\r\nName each compound.\r\n
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        1. \r\n
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          \"image\"<\/div>\r\n<\/div><\/li>\r\n \t
        2. \r\n
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          \"image\"<\/div>\r\n<\/div><\/li>\r\n \t
        3. \r\n
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          \"image\"<\/div>\r\n<\/div>\r\n
          <\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n
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          Example 2<\/h3>\r\n

          Draw the structure for each compound.<\/p>\r\n\r\n

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          1. 2,3-dimethylbutane<\/li>\r\n \t
          2. 4-isopropyl-2-methylheptane<\/li>\r\n<\/ol>\r\n

            Solution<\/p>\r\n

            In drawing structures, always start with the parent chain.<\/p>\r\n\r\n

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            1. \r\n

              The parent chain is butane, indicating four carbon atoms in the LCC.<\/p>\r\n\r\n

              \"image\"<\/div>\r\n

              Then add the groups at their proper positions. You can number the parent chain from either direction as long as you are consistent; just don\u2019t change directions before the structure is done. The name indicates two methyl (CH3<\/sub>) groups, one on the second carbon atom and one on the third.<\/p>\r\n\r\n

              \"image\"<\/div>\r\n

              Finally, fill in all the hydrogen atoms, keeping in mind that each carbon atom must have four bonds.<\/p>\r\n\r\n

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

              The parent chain is heptane in this case, indicating seven carbon atoms in the LCC.<\/p>\r\n\u2013C\u2013C\u2013C\u2013C\u2013C\u2013C\u2013C\u2013<\/span><\/span>\r\n

              Adding the groups at their proper positions gives<\/p>\r\n\r\n

              \"image\"<\/div>\r\n

              Filling in all the hydrogen atoms gives the following condensed structural formulas:<\/p>\r\n\r\n

              \"image\"<\/div>\r\n

              Note that the bonds (dashes) can be shown or not; sometimes they are needed for spacing.<\/p>\r\n<\/li>\r\n<\/ol>\r\n<\/div>\r\n

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              Skill-Building Exercise<\/h3>\r\nDraw the structure for each compound.\r\n
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                4-ethyloctane<\/p>\r\n\r\n<\/div><\/li>\r\n \t

              2. \r\n
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                3-ethyl-2-methylpentane<\/p>\r\n\r\n<\/div><\/li>\r\n \t

              3. \r\n
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                3,3,5-trimethylheptane<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n

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                Concept Review Exercises<\/h3>\r\n
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                  What is a CH3<\/sub> group called when it is attached to a chain of carbon atoms\u2014a substituent or a functional group?<\/p>\r\n\r\n<\/div><\/li>\r\n \t

                2. \r\n
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                  Which type of name uses numbers to locate substituents\u2014common names or IUPAC names?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n

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                  Answers<\/h3>\r\n[reveal-answer q=\"33609\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"33609\"]\r\n
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                  1. substituent<\/li>\r\n \t
                  2. IUPAC names\u00a0[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n
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                    Key Takeaway<\/h3>\r\n<\/div>\r\n
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