{"id":596,"date":"2017-10-04T21:02:22","date_gmt":"2017-10-04T21:02:22","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/?post_type=chapter&#038;p=596"},"modified":"2018-10-03T17:32:12","modified_gmt":"2018-10-03T17:32:12","slug":"monosubstituted-cylcohexanes","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/chapter\/monosubstituted-cylcohexanes\/","title":{"raw":"Monosubstituted Cylcohexanes","rendered":"Monosubstituted Cylcohexanes"},"content":{"raw":"<div class=\"elm-header\">\r\n<div class=\"elm-header-custom\">\r\n<div class=\"textbox learning-objectives\">\r\n<h3>Objectives<\/h3>\r\n<div id=\"elm-main-content\" class=\"elm-content-container\">\r\n<div>\r\n<div id=\"skills\">\r\n\r\nAfter completing this section, you should be able to\r\n<ol>\r\n \t<li>account for the greater stability of the equatorial conformers of monosubstituted cyclohexanes compared to their axial counterparts, using the concept of 1,3\u2011diaxial interaction.<\/li>\r\n \t<li>compare the gauche interactions in butane with the 1,3\u2011diaxial interactions in the axial conformer of methylcyclohexane.<\/li>\r\n \t<li>arrange a given list of substituents in increasing or decreasing order of 1,3\u2011diaxial interactions.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"elm-main-content\" class=\"elm-content-container\">\r\n<div>\r\n<div>\r\n<div class=\"textbox key-takeaways\">\r\n<h3>Key TERms<\/h3>\r\nMake certain that you can define, and use in context, the key term below.\r\n<ul>\r\n \t<li>1,3\u2011diaxial interaction<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div id=\"note\">\r\n<div class=\"textbox\">\r\n<h3 class=\"boxtitle\">Study Notes<\/h3>\r\n<em>1,3-Diaxial interactions<\/em> are steric interactions between an axial substituent located on carbon atom 1 of a cyclohexane ring and the hydrogen atoms (or other substituents) located on carbon atoms 3 and 5.\r\n\r\nBe prepared to draw Newman-type projections for cyclohexane derivatives as the one shown for methylcyclohexane. Note that this is similar to the Newman projections from chapter 3 such as <em>n<\/em>-butane.\r\n\r\n<img src=\"https:\/\/chem.libretexts.org\/LibreTexts\/Athabasca_University\/Chemistry_350%3A_Organic_Chemistry_I\/Chapter_4%3A_Organic_Compounds%3A_Cycloalkanes_and_their_Stereochemistry\/\/LibreTexts\/Athabasca_University\/Chemistry_350:_Organic_Chemistry_I\/Chapter_4:_Organic_Compounds:_Cycloalkanes_and_their_Stereochemistry\/4.7_Conformations_of_Monosubstituted_Cyclohexanes##fixme\" alt=\"Newman projections of methylcyclohexane and n-butane\" \/>\r\n\r\nNewman projections of methylcyclohexane and <em>n<\/em>\u2011butane\r\n\r\n<\/div>\r\n<\/div>\r\nBecause axial bonds are parallel to each other, substituents larger than hydrogen generally suffer greater steric crowding when they are oriented axial rather than equatorial. Consequently, <strong><em>substituted cyclohexanes will preferentially adopt conformations in which the larger substituents assume equatorial orientation<\/em><\/strong>.\r\n\r\n<img class=\"internal default aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/1518\/2017\/10\/04210204\/image045.png\" alt=\"image045.png\" width=\"474px\" height=\"140px\" \/>\r\n\r\nWhen the methyl group in the structure above occupies an axial position it suffers steric crowding by the two axial hydrogens located on the same side of the ring.\r\n\r\n<img class=\"internal default aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/1518\/2017\/10\/04210206\/image048.png\" alt=\"image048.png\" width=\"188px\" height=\"183px\" \/>\r\n\r\nThe conformation in which the methyl group is equatorial is more stable, and thus the equilibrium lies in this direction.\r\n\r\nThe relative steric hindrance experienced by different substituent groups oriented in an axial versus equatorial location on cyclohexane may be determined by the conformational equilibrium of the compound. The corresponding equilibrium constant is related to the energy difference between the conformers, and collecting such data allows us to evaluate the relative tendency of substituents to exist in an equatorial or axial location.A table of these free energy values (sometimes referred to as A values) may be examined by clicking <a class=\"external\" title=\"http:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/VirtTxtJml\/confengy.htm\" href=\"http:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/VirtTxtJml\/confengy.htm\" target=\"_blank\" rel=\"external nofollow noopener\">here<\/a>.\r\n\r\nLooking at the energy values in this table, it is clear that the apparent \"size\" of a substituent (in terms of its preference for equatorial over axial orientation)\u00a0 is influenced by its width and bond length to cyclohexane, as evidenced by the fact that an axial vinyl group is less hindered than ethyl, and iodine slightly less than chlorine.\r\n\r\nWe noted earlier that cycloalkanes having two or more substituents on different ring carbon atoms exist as a pair (sometimes more) of configurational stereoisomers. Now we must examine the way in which favorable ring conformations influence the properties of the configurational isomers. Remember, configurational stereoisomers are stable and do not easily interconvert, whereas, conformational isomers normally interconvert rapidly. In examining possible structures for substituted cyclohexanes, it is useful to follow two principles:\r\n<ol start=\"1\">\r\n \t<li>Chair conformations are generally more stable than other possibilities.<\/li>\r\n \t<li>Substituents on chair conformers prefer to occupy equatorial positions due to the increased steric hindrance of axial locations.<\/li>\r\n<\/ol>\r\n<table style=\"margin: auto;border-spacing: 1px;width: 702px\" border=\"1\" cellpadding=\"1\"><caption><em><strong>Table 1:<\/strong> A Selection of AG\u00b0 Values for the Change from Axial to Equatorial Orientation of Substituents for Monosubstituted Cyclohexanes<\/em><\/caption>\r\n<tbody>\r\n<tr>\r\n<td><strong>Substituent<\/strong><\/td>\r\n<td><strong>$$-\\Delta{G}^o$$ kcal\/mol<\/strong><\/td>\r\n<td><strong>Substituent<\/strong><\/td>\r\n<td><strong>$$-\\Delta{G}^o$$ kcal\/mol<\/strong><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{CH_3\\bond{-}}$$<\/td>\r\n<td>1.7<\/td>\r\n<td>$$\\ce{O_2N\\bond{-}}$$<\/td>\r\n<td>1.1<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{CH_2H_5\\bond{-}}$$<\/td>\r\n<td>1.8<\/td>\r\n<td>$$\\ce{N#C\\bond{-}}$$<\/td>\r\n<td>0.2<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{(CH_3)_2CH\\bond{-}}$$<\/td>\r\n<td>2.2<\/td>\r\n<td>$$\\ce{CH_3O\\bond{-}}$$<\/td>\r\n<td>0.5<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{(CH_3)_3C\\bond{-}}$$<\/td>\r\n<td>$$\\geq 5.0$$<\/td>\r\n<td><img src=\"https:\/\/chem.libretexts.org\/LibreTexts\/Athabasca_University\/Chemistry_350%3A_Organic_Chemistry_I\/Chapter_4%3A_Organic_Compounds%3A_Cycloalkanes_and_their_Stereochemistry\/src#fixme\" alt=\"image\" width=\"99px\" height=\"67px\" \/><\/td>\r\n<td>0.7<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{F\\bond{-}}$$<\/td>\r\n<td>0.3<\/td>\r\n<td><img src=\"https:\/\/chem.libretexts.org\/LibreTexts\/Athabasca_University\/Chemistry_350%3A_Organic_Chemistry_I\/Chapter_4%3A_Organic_Compounds%3A_Cycloalkanes_and_their_Stereochemistry\/src#fixme\" alt=\"image\" width=\"88px\" height=\"68px\" \/><\/td>\r\n<td>1.3<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{Cl\\bond{-}}$$<\/td>\r\n<td>0.5<\/td>\r\n<td>$$\\ce{C_6H_5\\bond{-}}$$<\/td>\r\n<td>3.0<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{Br\\bond{-}}$$<\/td>\r\n<td>0.5<\/td>\r\n<td><\/td>\r\n<td><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>$$\\ce{I\\bond{-}}$$<\/td>\r\n<td>0.5<\/td>\r\n<td><\/td>\r\n<td><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<div id=\"section_1\">\r\n<h3 class=\"editable\">Chlorocyclohexane<\/h3>\r\nThis is an example of the next level of complexity, a mono-substituted cycloalkane. See Fig 3.\r\n\r\n[caption id=\"\" align=\"aligncenter\" width=\"261\"]<img src=\"http:\/\/bbruner.org\/obc\/ring_fig\/ring_f3.gif#fixme\" alt=\"Chlorocyclohexane: simple hexagon and chair structures, showing hydrogen atoms.\" width=\"261\" height=\"82\" \/> Figure 3:[\/caption]\r\n\r\nSo what is new here? Not much, with the hexagon formula, Fig 3A. That type of formula shows the basic \"connectivity\" of the atoms -- who is connected to whom. This chemical has one Cl on the ring, and it does not matter where we show it. There is now only one H on that C, but since we are not showing H explicitly here, that is not an issue in drawing the structure. (It is an issue when you look at it and want to count H.)\r\n\r\nWith the chair formula (Fig 3B), which shows information not only about connectivity but also about conformation, there is important new information here. In a chair, there are two \"types\" of substituents: those pointing up or down, and called axial, and those pointing \"outward\", and called equatorial. I have shown the chlorine atom in an equatorial position. Why? Two reasons: it is what we would predict, and it is what is found. Why do we predict that the Cl is equatorial? Because it is bigger than H, and there is more room in the equatorial positions.\r\n<div>\r\n<div class=\"textbox shaded\">\r\n<div id=\"section_1\">\r\n<div>\r\n<h4 class=\"boxtitle\"><em>Helpful<\/em><em> Hints<\/em><\/h4>\r\nIf possible, examine a physical model of cyclohexane and chlorocyclohexane, so that you can see the axial and equatorial positions. Common ball and stick models are fine for this. It should be easy to see that the three axial H on one side can get very near each other.\r\n\r\nIf you do not have access to physical models, examining computer models can also be useful. When putting substituents on chair structures, I encourage you to use the four corner positions of the chair as much as possible. It is easier to see the axial and equatorial relationship at the corners.\r\n\r\nIn Fig 3B I have shown the H atom that is on the same carbon as the Cl atom. This is perhaps not necessary, since the correct number of H atoms is understood, by counting bonds on C. But showing the H explicitly at key C atoms helps to make the structure clearer. This may be particularly important with hand-drawn structures. I often see structures where I am not sure whether a particular atom is shown axial or equatorial. But if both atoms at the position (the H as well as the Cl) are shown, then hopefully it becomes clearer which is which. I also encourage students who are not sure of their art work to annotate their drawing. Say what you mean. That allows me to distinguish whether you are unsure which direction things point or simply unsure how to draw them.)\r\n\r\nFor notes on how to draw chairs (by hand or using a drawing program), see the section <a class=\"external\" title=\"http:\/\/bbruner.org\/obc\/rings.htm#DrawChair\" href=\"http:\/\/bbruner.org\/obc\/rings.htm#DrawChair\" target=\"_blank\" rel=\"external nofollow noopener\"> E.2. Note: How to draw chairs<\/a>.\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"section_2\">\r\n<div class=\"textbox exercises\">\r\n<h3>Exercises<\/h3>\r\n<div id=\"section_2\">\r\n<div id=\"s61691\">\r\n<div id=\"section_28\">\r\n<h3 id=\"Questions-61691\">Question<\/h3>\r\nIn the molecule, cyclohexyl ethyne there is little steric strain, why?\r\n\r\n<\/div>\r\n<div id=\"section_29\">\r\n<h3 id=\"Solutions-61691\">Solution<\/h3>\r\n[reveal-answer q=\"511415\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"511415\"]The ethyne group is linear and therefore does not affect the hydrogens in the 1,3 positions to say to the extent as a bulkier or a bent group (e.g. ethene group) would. This leads to less of a strain on the molecule.<img class=\"internal default aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/1518\/2017\/10\/04210209\/4.7.png\" alt=\"\" width=\"499\" height=\"150\" \/>\r\n\r\n[\/hidden-answer]\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"section_3\">\r\n<h3 class=\"editable\">Contributors<\/h3>\r\n<ul>\r\n \t<li><a class=\"external\" title=\"http:\/\/science.athabascau.ca\/staff-pages\/dietmark\" href=\"http:\/\/science.athabascau.ca\/staff-pages\/dietmark\" target=\"_blank\" rel=\"external nofollow noopener\">Dr. Dietmar Kennepohl<\/a> FCIC (Professor of Chemistry, <a class=\"external\" title=\"http:\/\/www.athabascau.ca\/\" href=\"http:\/\/www.athabascau.ca\/\" target=\"_blank\" rel=\"external nofollow noopener\">Athabasca University<\/a>)<\/li>\r\n \t<li>Prof. Steven Farmer (<a class=\"external\" title=\"http:\/\/www.sonoma.edu\" href=\"http:\/\/www.sonoma.edu\" target=\"_blank\" rel=\"external nofollow noopener\">Sonoma State University<\/a>)<\/li>\r\n<\/ul>\r\n<ul>\r\n \t<li>Robert Bruner (<a class=\"external\" title=\"http:\/\/bbruner.org\" href=\"http:\/\/bbruner.org\" target=\"_blank\" rel=\"external nofollow noopener\">http:\/\/bbruner.org<\/a>)<\/li>\r\n<\/ul>\r\n<ul>\r\n \t<li><a title=\"Organic_Chemistry_With_a_Biological_Emphasis\" href=\"https:\/\/chem.libretexts.org\/Textbook_Maps\/Organic_Chemistry_Textbook_Maps\/Map%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)\" rel=\"internal\">Organic Chemistry With a Biological Emphasis <\/a>by\u00a0<a class=\"external\" title=\"http:\/\/facultypages.morris.umn.edu\/~soderbt\/\" href=\"http:\/\/facultypages.morris.umn.edu\/%7Esoderbt\/\" target=\"_blank\" rel=\"external nofollow noopener\">Tim Soderberg<\/a>\u00a0(University of Minnesota, Morris)<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div class=\"elm-header\">\n<div class=\"elm-header-custom\">\n<div class=\"textbox learning-objectives\">\n<h3>Objectives<\/h3>\n<div id=\"elm-main-content\" class=\"elm-content-container\">\n<div>\n<div id=\"skills\">\n<p>After completing this section, you should be able to<\/p>\n<ol>\n<li>account for the greater stability of the equatorial conformers of monosubstituted cyclohexanes compared to their axial counterparts, using the concept of 1,3\u2011diaxial interaction.<\/li>\n<li>compare the gauche interactions in butane with the 1,3\u2011diaxial interactions in the axial conformer of methylcyclohexane.<\/li>\n<li>arrange a given list of substituents in increasing or decreasing order of 1,3\u2011diaxial interactions.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"elm-main-content\" class=\"elm-content-container\">\n<div>\n<div>\n<div class=\"textbox key-takeaways\">\n<h3>Key TERms<\/h3>\n<p>Make certain that you can define, and use in context, the key term below.<\/p>\n<ul>\n<li>1,3\u2011diaxial interaction<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div id=\"note\">\n<div class=\"textbox\">\n<h3 class=\"boxtitle\">Study Notes<\/h3>\n<p><em>1,3-Diaxial interactions<\/em> are steric interactions between an axial substituent located on carbon atom 1 of a cyclohexane ring and the hydrogen atoms (or other substituents) located on carbon atoms 3 and 5.<\/p>\n<p>Be prepared to draw Newman-type projections for cyclohexane derivatives as the one shown for methylcyclohexane. Note that this is similar to the Newman projections from chapter 3 such as <em>n<\/em>-butane.<\/p>\n<p><img decoding=\"async\" src=\"https:\/\/chem.libretexts.org\/LibreTexts\/Athabasca_University\/Chemistry_350%3A_Organic_Chemistry_I\/Chapter_4%3A_Organic_Compounds%3A_Cycloalkanes_and_their_Stereochemistry\/\/LibreTexts\/Athabasca_University\/Chemistry_350:_Organic_Chemistry_I\/Chapter_4:_Organic_Compounds:_Cycloalkanes_and_their_Stereochemistry\/4.7_Conformations_of_Monosubstituted_Cyclohexanes##fixme\" alt=\"Newman projections of methylcyclohexane and n-butane\" \/><\/p>\n<p>Newman projections of methylcyclohexane and <em>n<\/em>\u2011butane<\/p>\n<\/div>\n<\/div>\n<p>Because axial bonds are parallel to each other, substituents larger than hydrogen generally suffer greater steric crowding when they are oriented axial rather than equatorial. Consequently, <strong><em>substituted cyclohexanes will preferentially adopt conformations in which the larger substituents assume equatorial orientation<\/em><\/strong>.<\/p>\n<p><img decoding=\"async\" class=\"internal default aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/1518\/2017\/10\/04210204\/image045.png\" alt=\"image045.png\" width=\"474px\" height=\"140px\" \/><\/p>\n<p>When the methyl group in the structure above occupies an axial position it suffers steric crowding by the two axial hydrogens located on the same side of the ring.<\/p>\n<p><img decoding=\"async\" class=\"internal default aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/1518\/2017\/10\/04210206\/image048.png\" alt=\"image048.png\" width=\"188px\" height=\"183px\" \/><\/p>\n<p>The conformation in which the methyl group is equatorial is more stable, and thus the equilibrium lies in this direction.<\/p>\n<p>The relative steric hindrance experienced by different substituent groups oriented in an axial versus equatorial location on cyclohexane may be determined by the conformational equilibrium of the compound. The corresponding equilibrium constant is related to the energy difference between the conformers, and collecting such data allows us to evaluate the relative tendency of substituents to exist in an equatorial or axial location.A table of these free energy values (sometimes referred to as A values) may be examined by clicking <a class=\"external\" title=\"http:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/VirtTxtJml\/confengy.htm\" href=\"http:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/VirtTxtJml\/confengy.htm\" target=\"_blank\" rel=\"external nofollow noopener\">here<\/a>.<\/p>\n<p>Looking at the energy values in this table, it is clear that the apparent &#8220;size&#8221; of a substituent (in terms of its preference for equatorial over axial orientation)\u00a0 is influenced by its width and bond length to cyclohexane, as evidenced by the fact that an axial vinyl group is less hindered than ethyl, and iodine slightly less than chlorine.<\/p>\n<p>We noted earlier that cycloalkanes having two or more substituents on different ring carbon atoms exist as a pair (sometimes more) of configurational stereoisomers. Now we must examine the way in which favorable ring conformations influence the properties of the configurational isomers. Remember, configurational stereoisomers are stable and do not easily interconvert, whereas, conformational isomers normally interconvert rapidly. In examining possible structures for substituted cyclohexanes, it is useful to follow two principles:<\/p>\n<ol start=\"1\">\n<li>Chair conformations are generally more stable than other possibilities.<\/li>\n<li>Substituents on chair conformers prefer to occupy equatorial positions due to the increased steric hindrance of axial locations.<\/li>\n<\/ol>\n<table style=\"margin: auto;border-spacing: 1px;width: 702px\" cellpadding=\"1\">\n<caption><em><strong>Table 1:<\/strong> A Selection of AG\u00b0 Values for the Change from Axial to Equatorial Orientation of Substituents for Monosubstituted Cyclohexanes<\/em><\/caption>\n<tbody>\n<tr>\n<td><strong>Substituent<\/strong><\/td>\n<td><strong>$$-\\Delta{G}^o$$ kcal\/mol<\/strong><\/td>\n<td><strong>Substituent<\/strong><\/td>\n<td><strong>$$-\\Delta{G}^o$$ kcal\/mol<\/strong><\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{CH_3\\bond{-}}$$<\/td>\n<td>1.7<\/td>\n<td>$$\\ce{O_2N\\bond{-}}$$<\/td>\n<td>1.1<\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{CH_2H_5\\bond{-}}$$<\/td>\n<td>1.8<\/td>\n<td>$$\\ce{N#C\\bond{-}}$$<\/td>\n<td>0.2<\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{(CH_3)_2CH\\bond{-}}$$<\/td>\n<td>2.2<\/td>\n<td>$$\\ce{CH_3O\\bond{-}}$$<\/td>\n<td>0.5<\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{(CH_3)_3C\\bond{-}}$$<\/td>\n<td>$$\\geq 5.0$$<\/td>\n<td><img decoding=\"async\" src=\"https:\/\/chem.libretexts.org\/LibreTexts\/Athabasca_University\/Chemistry_350%3A_Organic_Chemistry_I\/Chapter_4%3A_Organic_Compounds%3A_Cycloalkanes_and_their_Stereochemistry\/src#fixme\" alt=\"image\" width=\"99px\" height=\"67px\" \/><\/td>\n<td>0.7<\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{F\\bond{-}}$$<\/td>\n<td>0.3<\/td>\n<td><img decoding=\"async\" src=\"https:\/\/chem.libretexts.org\/LibreTexts\/Athabasca_University\/Chemistry_350%3A_Organic_Chemistry_I\/Chapter_4%3A_Organic_Compounds%3A_Cycloalkanes_and_their_Stereochemistry\/src#fixme\" alt=\"image\" width=\"88px\" height=\"68px\" \/><\/td>\n<td>1.3<\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{Cl\\bond{-}}$$<\/td>\n<td>0.5<\/td>\n<td>$$\\ce{C_6H_5\\bond{-}}$$<\/td>\n<td>3.0<\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{Br\\bond{-}}$$<\/td>\n<td>0.5<\/td>\n<td><\/td>\n<td><\/td>\n<\/tr>\n<tr>\n<td>$$\\ce{I\\bond{-}}$$<\/td>\n<td>0.5<\/td>\n<td><\/td>\n<td><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<div id=\"section_1\">\n<h3 class=\"editable\">Chlorocyclohexane<\/h3>\n<p>This is an example of the next level of complexity, a mono-substituted cycloalkane. See Fig 3.<\/p>\n<div style=\"width: 271px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"http:\/\/bbruner.org\/obc\/ring_fig\/ring_f3.gif#fixme\" alt=\"Chlorocyclohexane: simple hexagon and chair structures, showing hydrogen atoms.\" width=\"261\" height=\"82\" \/><\/p>\n<p class=\"wp-caption-text\">Figure 3:<\/p>\n<\/div>\n<p>So what is new here? Not much, with the hexagon formula, Fig 3A. That type of formula shows the basic &#8220;connectivity&#8221; of the atoms &#8212; who is connected to whom. This chemical has one Cl on the ring, and it does not matter where we show it. There is now only one H on that C, but since we are not showing H explicitly here, that is not an issue in drawing the structure. (It is an issue when you look at it and want to count H.)<\/p>\n<p>With the chair formula (Fig 3B), which shows information not only about connectivity but also about conformation, there is important new information here. In a chair, there are two &#8220;types&#8221; of substituents: those pointing up or down, and called axial, and those pointing &#8220;outward&#8221;, and called equatorial. I have shown the chlorine atom in an equatorial position. Why? Two reasons: it is what we would predict, and it is what is found. Why do we predict that the Cl is equatorial? Because it is bigger than H, and there is more room in the equatorial positions.<\/p>\n<div>\n<div class=\"textbox shaded\">\n<div id=\"section_1\">\n<div>\n<h4 class=\"boxtitle\"><em>Helpful<\/em><em> Hints<\/em><\/h4>\n<p>If possible, examine a physical model of cyclohexane and chlorocyclohexane, so that you can see the axial and equatorial positions. Common ball and stick models are fine for this. It should be easy to see that the three axial H on one side can get very near each other.<\/p>\n<p>If you do not have access to physical models, examining computer models can also be useful. When putting substituents on chair structures, I encourage you to use the four corner positions of the chair as much as possible. It is easier to see the axial and equatorial relationship at the corners.<\/p>\n<p>In Fig 3B I have shown the H atom that is on the same carbon as the Cl atom. This is perhaps not necessary, since the correct number of H atoms is understood, by counting bonds on C. But showing the H explicitly at key C atoms helps to make the structure clearer. This may be particularly important with hand-drawn structures. I often see structures where I am not sure whether a particular atom is shown axial or equatorial. But if both atoms at the position (the H as well as the Cl) are shown, then hopefully it becomes clearer which is which. I also encourage students who are not sure of their art work to annotate their drawing. Say what you mean. That allows me to distinguish whether you are unsure which direction things point or simply unsure how to draw them.)<\/p>\n<p>For notes on how to draw chairs (by hand or using a drawing program), see the section <a class=\"external\" title=\"http:\/\/bbruner.org\/obc\/rings.htm#DrawChair\" href=\"http:\/\/bbruner.org\/obc\/rings.htm#DrawChair\" target=\"_blank\" rel=\"external nofollow noopener\"> E.2. Note: How to draw chairs<\/a>.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"section_2\">\n<div class=\"textbox exercises\">\n<h3>Exercises<\/h3>\n<div id=\"section_2\">\n<div id=\"s61691\">\n<div id=\"section_28\">\n<h3 id=\"Questions-61691\">Question<\/h3>\n<p>In the molecule, cyclohexyl ethyne there is little steric strain, why?<\/p>\n<\/div>\n<div id=\"section_29\">\n<h3 id=\"Solutions-61691\">Solution<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q511415\">Show Answer<\/span><\/p>\n<div id=\"q511415\" class=\"hidden-answer\" style=\"display: none\">The ethyne group is linear and therefore does not affect the hydrogens in the 1,3 positions to say to the extent as a bulkier or a bent group (e.g. ethene group) would. This leads to less of a strain on the molecule.<img loading=\"lazy\" decoding=\"async\" class=\"internal default aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/1518\/2017\/10\/04210209\/4.7.png\" alt=\"\" width=\"499\" height=\"150\" \/><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"section_3\">\n<h3 class=\"editable\">Contributors<\/h3>\n<ul>\n<li><a class=\"external\" title=\"http:\/\/science.athabascau.ca\/staff-pages\/dietmark\" href=\"http:\/\/science.athabascau.ca\/staff-pages\/dietmark\" target=\"_blank\" rel=\"external nofollow noopener\">Dr. Dietmar Kennepohl<\/a> FCIC (Professor of Chemistry, <a class=\"external\" title=\"http:\/\/www.athabascau.ca\/\" href=\"http:\/\/www.athabascau.ca\/\" target=\"_blank\" rel=\"external nofollow noopener\">Athabasca University<\/a>)<\/li>\n<li>Prof. Steven Farmer (<a class=\"external\" title=\"http:\/\/www.sonoma.edu\" href=\"http:\/\/www.sonoma.edu\" target=\"_blank\" rel=\"external nofollow noopener\">Sonoma State University<\/a>)<\/li>\n<\/ul>\n<ul>\n<li>Robert Bruner (<a class=\"external\" title=\"http:\/\/bbruner.org\" href=\"http:\/\/bbruner.org\" target=\"_blank\" rel=\"external nofollow noopener\">http:\/\/bbruner.org<\/a>)<\/li>\n<\/ul>\n<ul>\n<li><a title=\"Organic_Chemistry_With_a_Biological_Emphasis\" href=\"https:\/\/chem.libretexts.org\/Textbook_Maps\/Organic_Chemistry_Textbook_Maps\/Map%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)\" rel=\"internal\">Organic Chemistry With a Biological Emphasis <\/a>by\u00a0<a class=\"external\" title=\"http:\/\/facultypages.morris.umn.edu\/~soderbt\/\" href=\"http:\/\/facultypages.morris.umn.edu\/%7Esoderbt\/\" target=\"_blank\" rel=\"external nofollow noopener\">Tim Soderberg<\/a>\u00a0(University of Minnesota, Morris)<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"author":311,"menu_order":14,"template":"","meta":{"_candela_citation":"[]","CANDELA_OUTCOMES_GUID":"","pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[],"contributor":[],"license":[],"class_list":["post-596","chapter","type-chapter","status-publish","hentry"],"part":21,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/596","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/wp\/v2\/users\/311"}],"version-history":[{"count":5,"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/596\/revisions"}],"predecessor-version":[{"id":2250,"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/596\/revisions\/2250"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/parts\/21"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/596\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/wp\/v2\/media?parent=596"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=596"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/wp\/v2\/contributor?post=596"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-mcc-organicchemistry\/wp-json\/wp\/v2\/license?post=596"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}