{"id":667926,"date":"2023-08-31T19:27:36","date_gmt":"2023-08-31T13:57:36","guid":{"rendered":"https:\/\/infinitylearn.com\/surge\/?p=667926"},"modified":"2023-08-31T19:27:58","modified_gmt":"2023-08-31T13:57:58","slug":"newman-projections-definition-models-examples","status":"publish","type":"post","link":"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/","title":{"rendered":"Newman Projections | Definition, Models &#038; Examples"},"content":{"rendered":"<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_37 counter-hierarchy ez-toc-counter ez-toc-grey ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title\">Table of Contents<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" style=\"display: none;\"><label for=\"item\" aria-label=\"Table of Content\"><span style=\"display: flex;align-items: center;width: 35px;height: 30px;justify-content: center;\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/label><input type=\"checkbox\" id=\"item\"><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1' style='display:block'><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Introduction_to_Newman_Projections\" title=\"Introduction to Newman Projections\">Introduction to Newman Projections<\/a><ul class='ez-toc-list-level-3'><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Definition_of_Newman_projection\" title=\"Definition of Newman projection\">Definition of Newman projection<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Newman_projection_formula\" title=\"Newman projection formula\">Newman projection formula<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Newman_projection_examples\" title=\"Newman projection examples\">Newman projection examples<\/a><ul class='ez-toc-list-level-4'><li class='ez-toc-heading-level-4'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Newman_projection_of_ethane\" title=\"Newman projection of ethane\">Newman projection of ethane<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-4'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Newman_projection_of_butane\" title=\"Newman projection of butane\">Newman projection of butane<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-4'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Cyclohexane_newman_projection\" title=\"Cyclohexane newman projection\">Cyclohexane newman projection<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Newman_projection_propane\" title=\"Newman projection propane\">Newman projection propane<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Newman_and_sawhorse_projection\" title=\"Newman and sawhorse projection\">Newman and sawhorse projection<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-10\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Complex_newman_projections\" title=\"Complex newman projections\">Complex newman projections<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-11\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Frequently_Asked_Questions_on_Newman_Projections\" title=\"Frequently Asked Questions on Newman Projections\">Frequently Asked Questions on Newman Projections<\/a><ul class='ez-toc-list-level-3'><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-12\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#What_is_Newman_projection\" title=\"What is Newman projection?\">What is Newman projection?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-13\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#Draw_newman_projection_formula_of_ethane\" title=\"Draw newman projection formula of ethane.\">Draw newman projection formula of ethane.<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-14\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#What_is_the_best_example_of_conformational_changes\" title=\"What is the best example of conformational changes?\">What is the best example of conformational changes?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-15\" href=\"https:\/\/infinitylearn.com\/surge\/topics\/newman-projections\/#What_is_an_example_of_a_saw_horse_projection_class_11\" title=\"What is an example of a saw horse projection class 11?\">What is an example of a saw horse projection class 11?<\/a><\/li><\/ul><\/li><\/ul><\/nav><\/div>\n<h2><span class=\"ez-toc-section\" id=\"Introduction_to_Newman_Projections\"><\/span>Introduction to Newman Projections<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Stereochemistry covers all important aspects of stereochemistry, beginning with the history of stereochemistry and moving on to discuss molecular geometry in terms of bond distances and dihedral angles, as well as the biological importance of chirality and its effect on taste, odor, agrochemicals, and pharmaceuticals, before moving on to the basic principles, conformations, and configurations.<\/p>\n<h3><span class=\"ez-toc-section\" id=\"Definition_of_Newman_projection\"><\/span>Definition of Newman projection<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>A Newman projection is a graphic that aids in the visualization of a molecule&#8217;s three-dimensional structure. This projection is most typically used to show the stereochemistry of alkanes since it focuses on a carbon-carbon bond.<\/p>\n<p>A Newman projection depicts the front-to-back conformation of a chemical bond, with the front atom represented by the junction of three lines (a dot) and the back atom represented by a circle.<\/p>\n<p>The front atom is referred to as proximal, whereas the back atom is referred to as distal. This style of representation vividly shows the dihedral angle formed by the proximal and distal atoms.<\/p>\n<h3><span class=\"ez-toc-section\" id=\"Newman_projection_formula\"><\/span>Newman projection formula<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>The molecules are viewed as superimposed circles in the Newman projection formula along the connection connecting the major carbon atoms. Short straight lines intersecting the center and circumference at an angle of 120\u00b0 represent the remaining connections in each carbonyl group.<\/p>\n<p>The center of the circle represents the front carbon atom, while the periphery represents the back carbon atom. The graphic below displays the Newman projections of ethane. There can only be one drawn circular.<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667927 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-formula.png\" alt=\"Newman projection formula\" width=\"361\" height=\"181\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-formula.png 361w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-formula-300x150.png 300w\" sizes=\"(max-width: 361px) 100vw, 361px\" \/><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Newman_projection_examples\"><\/span>Newman projection examples<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<h4><span class=\"ez-toc-section\" id=\"Newman_projection_of_ethane\"><\/span>Newman projection of ethane<span class=\"ez-toc-section-end\"><\/span><\/h4>\n<p>Newman projection of Ethane shows it has two conformations: staggered and eclipsed. The two ethane conformations, staggered and eclipsed, are distinct and should be in different energy levels.<\/p>\n<p>Also Check For:<\/p>\n<p><strong>Also Check Relevant Topics like:<\/strong><\/p>\n<p><a href=\"https:\/\/infinitylearn.com\/surge\/formulas\/chemistry-formulas\"><button class=\"btn btn-dark mx-2 my-2 px-4\" style=\"border-radius: 50px;\" type=\"button\">Chemistry Formulas<\/button><\/a> <a href=\"https:\/\/infinitylearn.com\/surge\/articles\/chemistry-articles\/\"><button class=\"btn btn-dark mx-2 my-2 px-4\" style=\"border-radius: 50px;\" type=\"button\">Chemistry Articles<\/button><\/a> <a href=\"https:\/\/infinitylearn.com\/surge\/topics\/principle-of-uv\/\"><button class=\"btn btn-dark mx-2 my-2 px-4\" style=\"border-radius: 50px;\" type=\"button\">Principle of UV<\/button><\/a> <a href=\"https:\/\/infinitylearn.com\/surge\/articles\/the-cannizzaro-reaction-key-points-mechanism-and-conditions\/\"><button class=\"btn btn-dark mx-2 my-2 px-4\" style=\"border-radius: 50px;\" type=\"button\">Cannizzaro Reaction<\/button><\/a><\/p>\n<p>In eclipsed conformations, the hydrogen atoms on the front carbon overlap with the H atoms on the back carbon, causing repulsion between the electrons of the two carbons&#8217; C-H bonds. Torsional strain, also known as eclipsing strain, is a form of repulsion. The Newman projection of ethane is mentioned below:<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667928 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-Ethane.png\" alt=\"Newman projection of Ethane\" width=\"559\" height=\"189\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-Ethane.png 559w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-Ethane-300x101.png 300w\" sizes=\"(max-width: 559px) 100vw, 559px\" \/><\/p>\n<p>The Potential Energy of <strong>Newman projection of Ethane<\/strong> vs. Angle of the Rotation around a C-C bond is given below:<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667929 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-Ethane-1.png\" alt=\"Newman projection of Ethane\" width=\"541\" height=\"327\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-Ethane-1.png 541w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-Ethane-1-300x181.png 300w\" sizes=\"(max-width: 541px) 100vw, 541px\" \/><\/p>\n<h4><span class=\"ez-toc-section\" id=\"Newman_projection_of_butane\"><\/span>Newman projection of butane<span class=\"ez-toc-section-end\"><\/span><\/h4>\n<p>The rotation of the C2-C3 bond in butane in the first staggered conformation, the two methyl groups are 180\u00b0 apart. This conformer is known as the anti conformer. In the opposite staggered conformer in the Newman projection of butane, both methyl groups flank each other.<\/p>\n<p>A gauche contact occurs when two adjacent big groups with a staggered conformation interact. Gauche interactions enhance the amount of energy of a conformer. Because the staggered anti conformer had no gauche interactions. It has less energy compared to the staggered gauche conformed. The Newman projection of butane is shown below:<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667930 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-butane.png\" alt=\"Newman projection of butane\" width=\"577\" height=\"331\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-butane.png 577w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-of-butane-300x172.png 300w\" sizes=\"(max-width: 577px) 100vw, 577px\" \/><\/p>\n<h4><span class=\"ez-toc-section\" id=\"Cyclohexane_newman_projection\"><\/span>Cyclohexane newman projection<span class=\"ez-toc-section-end\"><\/span><\/h4>\n<p>The most stable cycloalkane is cyclohexane. It is strain-free, which means there are no angle or torsional strains, and it has the same stability as chain alkanes. This exceptional stability is due to the peculiar conformation it assumes. The most stable cyclohexane conformation is known as the &#8220;chair&#8221; shape. The Newman projection of cyclohexane is shown below:<\/p>\n<h3><span class=\"ez-toc-section\" id=\"Newman_projection_propane\"><\/span><img loading=\"lazy\" class=\"alignnone wp-image-667931 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Cyclohexane-newman-projection.png\" alt=\"Cyclohexane newman projection\" width=\"658\" height=\"199\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Cyclohexane-newman-projection.png 658w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Cyclohexane-newman-projection-300x91.png 300w\" sizes=\"(max-width: 658px) 100vw, 658px\" \/>Newman projection propane<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>The distinction between propane and ethane is that propane has a methyl (CH3) group attached to the back carbon. However, the relative stability is unaffected, and the staggered conformer is more stable and has lower energy. The Newman projection of propane is shown below:<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667932 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-propane.png\" alt=\"Newman projection propane\" width=\"520\" height=\"346\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-propane.png 520w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-projection-propane-300x200.png 300w\" sizes=\"(max-width: 520px) 100vw, 520px\" \/><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Newman_and_sawhorse_projection\"><\/span>Newman and sawhorse projection<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>There are some differences in drawing Newman and sawhorse projection as shown below in the table:<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667933 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-and-sawhorse-projection.png\" alt=\"Newman and sawhorse projection\" width=\"559\" height=\"202\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-and-sawhorse-projection.png 559w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Newman-and-sawhorse-projection-300x108.png 300w\" sizes=\"(max-width: 559px) 100vw, 559px\" \/><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Complex_newman_projections\"><\/span>Complex newman projections<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>The Complex Newman projections of some of the molecules are given below:<\/p>\n<p><img loading=\"lazy\" class=\"alignnone wp-image-667934 size-full\" src=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Complex-newman-projections.png\" alt=\"Complex newman projections\" width=\"616\" height=\"409\" srcset=\"https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Complex-newman-projections.png 616w, https:\/\/infinitylearn.com\/surge\/wp-content\/uploads\/2023\/08\/Complex-newman-projections-300x199.png 300w\" sizes=\"(max-width: 616px) 100vw, 616px\" \/><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Frequently_Asked_Questions_on_Newman_Projections\"><\/span>Frequently Asked Questions on Newman Projections<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\t\t<section class=\"sc_fs_faq sc_card \">\n\t\t\t<div>\n\t\t\t\t<h3><span class=\"ez-toc-section\" id=\"What_is_Newman_projection\"><\/span>What is Newman projection?<span class=\"ez-toc-section-end\"><\/span><\/h3>\t\t\t\t<div>\n\t\t\t\t\t\t\t\t\t\t<p>\n\t\t\t\t\t\tA Newman projection depicts the conformation of a chemical bond from front to back, with the line representing the front atom and a circle indicating the back carbon. It is useful in alkane stereochemistry. The carbon atom near the front is referred to as proximal, while the atom at the back is referred to as distal. \t\t\t\t\t<\/p>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"sc_fs_faq sc_card \">\n\t\t\t<div>\n\t\t\t\t<h3><span class=\"ez-toc-section\" id=\"Draw_newman_projection_formula_of_ethane\"><\/span>Draw newman projection formula of ethane.<span class=\"ez-toc-section-end\"><\/span><\/h3>\t\t\t\t<div>\n\t\t\t\t\t\t\t\t\t\t<p>\n\t\t\t\t\t\tNewman projection formula for several ethane conformations: When an ethane molecule spins around its carbon-carbon single bond, it can form two extreme conformations: the staggered conformation and the eclipsed conformation.\t\t\t\t\t<\/p>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"sc_fs_faq sc_card \">\n\t\t\t<div>\n\t\t\t\t<h3><span class=\"ez-toc-section\" id=\"What_is_the_best_example_of_conformational_changes\"><\/span>What is the best example of conformational changes?<span class=\"ez-toc-section-end\"><\/span><\/h3>\t\t\t\t<div>\n\t\t\t\t\t\t\t\t\t\t<p>\n\t\t\t\t\t\tGuanine and adenine nucleotide triphosphatases (NTPases) are two of the most well-known proteins that undergo large-scale conformational changes to regulate cell functions. \t\t\t\t\t<\/p>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"sc_fs_faq sc_card \">\n\t\t\t<div>\n\t\t\t\t<h3><span class=\"ez-toc-section\" id=\"What_is_an_example_of_a_saw_horse_projection_class_11\"><\/span>What is an example of a saw horse projection class 11?<span class=\"ez-toc-section-end\"><\/span><\/h3>\t\t\t\t<div>\n\t\t\t\t\t\t\t\t\t\t<p>\n\t\t\t\t\t\tA sawhorse projection is the appearance of a molecule with a certain Carbon-Carbon bond. Both the front and back carbon groups can be drawn with sticks at a 120-degree angle. \t\t\t\t\t<\/p>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/section>\n\t\t\n<script type=\"application\/ld+json\">\n\t{\n\t\t\"@context\": \"https:\/\/schema.org\",\n\t\t\"@type\": \"FAQPage\",\n\t\t\"mainEntity\": [\n\t\t\t\t\t{\n\t\t\t\t\"@type\": \"Question\",\n\t\t\t\t\"name\": \"What is Newman projection?\",\n\t\t\t\t\"acceptedAnswer\": {\n\t\t\t\t\t\"@type\": \"Answer\",\n\t\t\t\t\t\"text\": \"A Newman projection depicts the conformation of a chemical bond from front to back, with the line representing the front atom and a circle indicating the back carbon. It is useful in alkane stereochemistry. The carbon atom near the front is referred to as proximal, while the atom at the back is referred to as distal.\"\n\t\t\t\t\t\t\t\t\t}\n\t\t\t}\n\t\t\t,\t\t\t\t{\n\t\t\t\t\"@type\": \"Question\",\n\t\t\t\t\"name\": \"Draw newman projection formula of ethane.\",\n\t\t\t\t\"acceptedAnswer\": {\n\t\t\t\t\t\"@type\": \"Answer\",\n\t\t\t\t\t\"text\": \"Newman projection formula for several ethane conformations: When an ethane molecule spins around its carbon-carbon single bond, it can form two extreme conformations: the staggered conformation and the eclipsed conformation.\"\n\t\t\t\t\t\t\t\t\t}\n\t\t\t}\n\t\t\t,\t\t\t\t{\n\t\t\t\t\"@type\": \"Question\",\n\t\t\t\t\"name\": \"What is the best example of conformational changes?\",\n\t\t\t\t\"acceptedAnswer\": {\n\t\t\t\t\t\"@type\": \"Answer\",\n\t\t\t\t\t\"text\": \"Guanine and adenine nucleotide triphosphatases (NTPases) are two of the most well-known proteins that undergo large-scale conformational changes to regulate cell functions.\"\n\t\t\t\t\t\t\t\t\t}\n\t\t\t}\n\t\t\t,\t\t\t\t{\n\t\t\t\t\"@type\": \"Question\",\n\t\t\t\t\"name\": \"What is an example of a saw horse projection class 11?\",\n\t\t\t\t\"acceptedAnswer\": {\n\t\t\t\t\t\"@type\": \"Answer\",\n\t\t\t\t\t\"text\": \"A sawhorse projection is the appearance of a molecule with a certain Carbon-Carbon bond. Both the front and back carbon groups can be drawn with sticks at a 120-degree angle.\"\n\t\t\t\t\t\t\t\t\t}\n\t\t\t}\n\t\t\t\t\t\t]\n\t}\n<\/script>\n\n","protected":false},"excerpt":{"rendered":"<p>Introduction to Newman Projections Stereochemistry covers all important aspects of stereochemistry, beginning with the history of stereochemistry and moving on [&hellip;]<\/p>\n","protected":false},"author":53,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_yoast_wpseo_focuskw":"Newman Projections","_yoast_wpseo_title":"Newman Projection - How to Draw Newman Projection","_yoast_wpseo_metadesc":"Newman projection of butane, the molecule is viewed along the C-C bond, with the front C atom bonded to the H and CH3 groups.","custom_permalink":"topics\/newman-projections\/"},"categories":[8593,8591],"tags":[8815,8810,8816,8813,8811,8807,8809,8808,8812,8814],"table_tags":[],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v17.9 - 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