{"id":25953,"date":"2025-06-19T08:29:39","date_gmt":"2025-06-19T08:29:39","guid":{"rendered":"https:\/\/gaviki.com\/blog\/?p=25953"},"modified":"2025-06-19T08:29:40","modified_gmt":"2025-06-19T08:29:40","slug":"bond-length-in-nitric-oxide-no-is-115-pm-molecular-nitrogen-n2-and-nitrosyl-ion-no-display-bonds-that-are-substantially-shorter-109-4-and-106-pm-respectively","status":"publish","type":"post","link":"https:\/\/gaviki.com\/blog\/bond-length-in-nitric-oxide-no-is-115-pm-molecular-nitrogen-n2-and-nitrosyl-ion-no-display-bonds-that-are-substantially-shorter-109-4-and-106-pm-respectively\/","title":{"rendered":"Bond length in nitric oxide (NO) is 115 pm. Molecular nitrogen (N2) and nitrosyl ion (NO + ) display bonds that are substantially shorter (109.4 and 106 pm, respectively)."},"content":{"rendered":"\n<p>Bond length in nitric oxide (NO) is 115 pm. Molecular nitrogen (N2) and nitrosyl ion (NO + ) display bonds that are substantially shorter (109.4 and 106 pm, respectively). Use molecular orbital theory to explain these differences.<\/p>\n\n\n\n<p><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-vivid-red-color\">The Correct Answer and Explanation is:<\/mark><\/strong><\/p>\n\n\n\n<p>The bond length differences between nitric oxide (NO), molecular nitrogen (N\u2082), and the nitrosyl ion (NO\u207a) can be explained using <strong>molecular orbital (MO) theory<\/strong>, which considers the behavior of electrons in molecular orbitals formed by the combination of atomic orbitals.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Molecular Orbital Configuration and Bond Order:<\/h3>\n\n\n\n<p><strong>1. Molecular nitrogen (N\u2082):<\/strong><\/p>\n\n\n\n<p>N\u2082 has 14 total electrons (7 from each nitrogen atom). Its molecular orbital configuration is:<\/p>\n\n\n\n<p>\u03c3(1s)\u00b2, \u03c3*(1s)\u00b2, \u03c3(2s)\u00b2, \u03c3*(2s)\u00b2, \u03c0(2p)\u2074, \u03c3(2p_z)\u00b2<\/p>\n\n\n\n<p>To find the bond order, we use the formula:<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><strong>Bond order = (Number of bonding electrons &#8211; Number of antibonding electrons) \/ 2<\/strong><\/p>\n<\/blockquote>\n\n\n\n<p>For N\u2082:<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>(10 bonding electrons &#8211; 4 antibonding electrons) \/ 2 = 3<\/p>\n<\/blockquote>\n\n\n\n<p>So, N\u2082 has a <strong>bond order of 3<\/strong>, indicating a <strong>triple bond<\/strong>. This results in a <strong>short bond length of 109.4 pm<\/strong>, because stronger bonds are shorter.<\/p>\n\n\n\n<p><strong>2. Nitric oxide (NO):<\/strong><\/p>\n\n\n\n<p>NO has 15 electrons (7 from N and 8 from O). The MO configuration is similar to N\u2082, but with an extra electron placed in the \u03c0*(2p) antibonding orbital:<\/p>\n\n\n\n<p>\u03c3(1s)\u00b2, \u03c3*(1s)\u00b2, \u03c3(2s)\u00b2, \u03c3*(2s)\u00b2, \u03c0(2p)\u2074, \u03c3(2p_z)\u00b2, \u03c0*(2p)\u00b9<\/p>\n\n\n\n<p>Bond order:<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>(10 bonding &#8211; 5 antibonding) \/ 2 = 2.5<\/p>\n<\/blockquote>\n\n\n\n<p>This <strong>bond order of 2.5<\/strong> results in a bond that is weaker than a triple bond, making the <strong>bond length longer (115 pm)<\/strong> than in N\u2082.<\/p>\n\n\n\n<p><strong>3. Nitrosyl ion (NO\u207a):<\/strong><\/p>\n\n\n\n<p>NO\u207a has 14 electrons (one less than NO). The electron removed is from the \u03c0*(2p) antibonding orbital:<\/p>\n\n\n\n<p>\u03c3(1s)\u00b2, \u03c3*(1s)\u00b2, \u03c3(2s)\u00b2, \u03c3*(2s)\u00b2, \u03c0(2p)\u2074, \u03c3(2p_z)\u00b2<\/p>\n\n\n\n<p>Bond order:<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>(10 bonding &#8211; 4 antibonding) \/ 2 = 3<\/p>\n<\/blockquote>\n\n\n\n<p>So, NO\u207a also has a <strong>bond order of 3<\/strong>, like N\u2082, leading to a <strong>shorter bond length (106 pm)<\/strong>.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Conclusion:<\/h3>\n\n\n\n<p>The differences in bond length are due to the number of electrons in antibonding orbitals. More electrons in antibonding orbitals lower bond order and increase bond length. Thus:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>NO\u207a: bond order 3 \u2192 shortest bond (106 pm)<\/li>\n\n\n\n<li>N\u2082: bond order 3 \u2192 short bond (109.4 pm)<\/li>\n\n\n\n<li>NO: bond order 2.5 \u2192 longer bond (115 pm)<\/li>\n<\/ul>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"722\" height=\"1024\" src=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner10-24.jpeg\" alt=\"\" class=\"wp-image-25954\" srcset=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner10-24.jpeg 722w, https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner10-24-212x300.jpeg 212w\" sizes=\"auto, (max-width: 722px) 100vw, 722px\" \/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Bond length in nitric oxide (NO) is 115 pm. Molecular nitrogen (N2) and nitrosyl ion (NO + ) display bonds that are substantially shorter (109.4 and 106 pm, respectively). Use molecular orbital theory to explain these differences. The Correct Answer and Explanation is: The bond length differences between nitric oxide (NO), molecular nitrogen (N\u2082), and [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-25953","post","type-post","status-publish","format-standard","hentry","category-quiz-questions"],"_links":{"self":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/25953","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/comments?post=25953"}],"version-history":[{"count":1,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/25953\/revisions"}],"predecessor-version":[{"id":25955,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/25953\/revisions\/25955"}],"wp:attachment":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/media?parent=25953"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/categories?post=25953"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/tags?post=25953"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}