{"id":897,"date":"2019-01-03T20:07:24","date_gmt":"2019-01-03T20:07:24","guid":{"rendered":"http:\/\/stage.clientden.com\/orbitalsnitrogen\/"},"modified":"2019-05-18T13:07:39","modified_gmt":"2019-05-18T13:07:39","slug":"orbitalsnitrogen","status":"publish","type":"page","link":"https:\/\/www.chemtube3d.com\/orbitalsnitrogen\/","title":{"rendered":"Molecular orbitals in Nitrogen"},"content":{"rendered":"<p><img loading=\"lazy\" src=\"..\/images\/clayden\/nitrogenorbitals.png\" alt=\"fluorine orbitals\" width=\"416\" height=\"420\" \/><\/p>\n<p>Use the buttons to display the 1s and 2p atomic orbitals that make up the molecular orbitals.<\/p>\n<p><script>\n\t       Jmol.jmolButton(jmolApplet0, <\/p>\n<\/p>\n<p class=\"load\">model\/ltf\/nitrogenSTO.spardir;spin on;\",\n\t      \"Reload Ball and Stick\");\n\t      Jmol.jmolButton(jmolApplet0, <\/p>\n<\/p>\n<p class=\"load\">model\/ltf\/nitrogenSTO.spardir;spin on;wireframe on;spacefill off;\",\n\t      <\/p>\n<\/p>\n<p class=\"load\">wireframe\");\nJmol.jmolButton(jmolApplet0, 'select (nitrogen);lcaoCartoon color white \"s\"',\n\t      <\/p>\n<\/p>\n<p class=\"load\">N 1s\");\n\t      \t   \t      Jmol.jmolButton(jmolApplet0, 'select (nitrogen);lcaoCartoon color white \"pz\" molecular',\n\t      \"Show pz orbitals\");\n\t      \t      Jmol.jmolButton(jmolApplet0, 'select (nitrogen);lcaoCartoon color yellow purple \"px\" molecular',\n\t      \"Show px orbitals\");\n\t      \t      Jmol.jmolButton(jmolApplet0, 'select (nitrogen);lcaoCartoon color red blue \"py\" molecular',\n\t      \"Show py orbitals\");\n<\/script><\/p>\n<p>There are four molecular orbitals derived from the 1s and 2s orbitals.<\/p>\n<p><script>\nJmol.jmolButton(jmolApplet0, <\/p>\n<\/p>\n<p class=\"load\">model\/ltf\/nitrogenSTO.spardir;spin on;\",\n\t      \"Reload Ball and Stick\");\nJmol.jmolButton(jmolApplet0, 'mo 1;',\n\t      \"Show 1s sigma\");\nJmol.jmolButton(jmolApplet0, 'mo 2;',\n\t      \"Show 1s sigma*\");\n\t      Jmol.jmolButton(jmolApplet0, 'mo 3;mo translucent',\n\t      \"Show 2s sigma\");\nJmol.jmolButton(jmolApplet0, 'mo 4;mo translucent',\n\t      \"Show 2s sigma*\");\n\t      <\/script><\/p>\n<p>The p orbitals combine to produce a sigma and two perpendicular pi bonds. Three <strong>filled<\/strong> bonding orbitals&#8230;<br \/>\n<script>\n\t      Jmol.jmolButton(jmolApplet0, 'mo 7;mo translucent',\n\t      \"Show 2p sigma\");\nJmol.jmolButton(jmolApplet0, 'mo 5;mo translucent;mo color yellow purple;',\n\t      \"Show 2px pi\");\n\t      Jmol.jmolButton(jmolApplet0, 'mo 6;mo translucent;mo color red blue;',\n\"Show 2py pi\");\n\t      <\/script><\/p>\n<p>&#8230; and three empty antibonding orbitals.<br \/>\n<script>\nJmol.jmolButton(jmolApplet0, 'mo 8;mo translucent;mo color yellow purple;',\n\t      \"Show 2px pi*\");\n\t      \t      Jmol.jmolButton(jmolApplet0, 'mo 9;mo translucent;mo color red blue;',\n\t      \"Show 2py pi*\");\n\t      Jmol.jmolButton(jmolApplet0, 'mo 10;mo translucent;',\n\t      \"Show 2p sigma*\");\n\t      \t      <\/script><\/p>\n<div><\/div>\n<p><script><\/p>\n<\/p>\n<div >\n<div >Jmol.jmolButton(jmolApplet0, &quot;spin off&quot;); Jmol.jmolButton(jmolApplet0, &quot;spin on&quot;);\nJmol.jmolButton(jmolApplet0, &quot;zoom 300&quot;); Jmol.jmolButton(jmolApplet0, &quot;zoom 100&quot;);<\/div>\n<\/div>\n<\/p>\n<p><\/script><\/p>\n<p><strong>Explore bonding orbitals in other small molecules<\/strong><\/p>\n<p><a href=\"orbitalshydrogen\/\">Hydrogen<\/a> | <a href=\"orbitalsfluorine\/\">Fluorine<\/a> | <a href=\"orbitalsnitrogen\/\">Nitrogen<\/a> | <a href=\"orbitalsHF\/\">Hydrogen Fluoride<\/a> | <a href=\"orbitalsCO\/\">Carbon Monoxide<\/a> | <a href=\"orbitalshybrid\/\">Methane<\/a> | <a href=\"orbitalsammonia\/\">Ammonia<\/a> | <a href=\"orbitalsethene\/\">Ethylene<\/a> | <a href=\"orbitalsacetylene\/\">Acetylene<\/a> | <a href=\"orbitalsallene\/\">Allene<\/a> | <a href=\"orbitalsformaldehyde\/\">Formaldehyde<\/a> | <a href=\"orbitalsbenzene\/\">Benzene<\/a><br \/>\n&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<div class=\"clayden\">\n<div class=\"clayden-bg\" style=\"background: url('http:\/\/www.chemtube3d.com\/weller7\/images\/weller100.jpg');\"><\/div>\n<div class=\"clayden-number\"><a href=\"WellerLink\/\" target=\"_new\">47<\/a><\/div>\n<\/p><\/div>\n<p><!-- InstanceEndEditable --><\/p>\n<p>&nbsp;<\/p>\n<p><!-- InstanceEnd --><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Use the buttons to display the 1s and 2p atomic orbitals that make up the molecular orbitals. There are four molecular orbitals derived from the 1s and 2s orbitals. The p orbitals combine to produce a sigma and two perpendicular pi bonds. Three filled bonding orbitals&#8230; &#8230; and three empty&#8230;<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"jsmoltwo.php","meta":[],"categories":[44,95],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v15.5 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Molecular orbitals in Nitrogen<\/title>\n<meta name=\"description\" content=\"Interactive 3D chemistry animations of reaction mechanisms and 3D models of chemical structures for students studying University courses and advanced school chemistry hosted by University of Liverpool\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.chemtube3d.com\/orbitalsnitrogen\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta 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