{"id":222309,"date":"2025-05-31T08:28:08","date_gmt":"2025-05-31T08:28:08","guid":{"rendered":"https:\/\/learnexams.com\/blog\/?p=222309"},"modified":"2025-05-31T08:28:10","modified_gmt":"2025-05-31T08:28:10","slug":"ch1202-3000-2000-1000-4","status":"publish","type":"post","link":"https:\/\/www.learnexams.com\/blog\/2025\/05\/31\/ch1202-3000-2000-1000-4\/","title":{"rendered":"CH1202 3000 2000 1000 4."},"content":{"rendered":"\n<p>1E. CH1202 3000 2000 1000 4. PUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUU 2.0 3. Wwwpo W Stand Wh Ards In Their Teatro LL 100 For Each Do The Following: Calculate The Index Of Hydrogen Deficiency (IHD), Label Each Spectra As The TYPE Of Spectra It Is, Label The Significant Peaks In Each Spectra, Determine The Structure And Draw A Box Around It.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/learnexams.com\/blog\/wp-content\/uploads\/2025\/05\/image-562-795x1024.png\" alt=\"\" class=\"wp-image-222310\"\/><\/figure>\n\n\n\n<p><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-ast-global-color-1-color\">The Correct Answer and Explanation is<\/mark><\/strong>:<\/p>\n\n\n\n<p>To solve this structure elucidation problem, we&#8217;ll go through each step using the molecular formula <strong>C\u2088H\u2081\u2082O\u2082<\/strong> and analyze the provided IR, \u00b9H NMR, and mass spectra.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">1. <strong>Index of Hydrogen Deficiency (IHD):<\/strong><\/h3>\n\n\n\n<p><strong>Formula:<\/strong> IHD=2C+2\u2212H2=2(8)+2\u2212122=62=3\\text{IHD} = \\frac{2C + 2 &#8211; H}{2} = \\frac{2(8) + 2 &#8211; 12}{2} = \\frac{6}{2} = 3<\/p>\n\n\n\n<p><strong>IHD = 3<\/strong>, suggesting combinations of rings and\/or double bonds (e.g., one ring and two double bonds, or one aromatic ring).<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">2. <strong>Spectra Identification:<\/strong><\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Top: Infrared (IR) Spectrum<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Broad peak near <strong>3400 cm\u207b\u00b9<\/strong>: O\u2013H stretch (likely alcohol)<\/li>\n\n\n\n<li>Sharp peak near <strong>1700 cm\u207b\u00b9<\/strong>: C=O stretch (carbonyl)<\/li>\n\n\n\n<li>Peaks near <strong>1200 cm\u207b\u00b9<\/strong>: C\u2013O stretch<\/li>\n<\/ul>\n\n\n\n<p><strong>Conclusion:<\/strong> The compound contains <strong>both an alcohol and a carbonyl<\/strong> group, likely a carboxylic acid or ester.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Middle: \u00b9H NMR Spectrum<\/strong><\/h4>\n\n\n\n<p>Key peaks:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>~4.1 ppm (quartet)<\/strong>: \u2013CH\u2082\u2013 near an electronegative atom (likely O)<\/li>\n\n\n\n<li><strong>~1.2 ppm (triplet)<\/strong>: \u2013CH\u2083 group next to \u2013CH\u2082\u2013 (suggests ethyl group)<\/li>\n\n\n\n<li><strong>~2.0 ppm (singlet)<\/strong>: CH\u2083\u2013CO\u2013 (methyl ketone or ester)<\/li>\n\n\n\n<li><strong>~7.2 ppm (multiplet)<\/strong>: Aromatic protons (4H, monosubstituted benzene ring)<\/li>\n<\/ul>\n\n\n\n<p><strong>Conclusion:<\/strong> Signals are consistent with:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Ethyl ester group (triplet\/quartet)<\/li>\n\n\n\n<li>Aromatic ring with 4H (suggesting a disubstituted benzene)<\/li>\n\n\n\n<li>Possibly para-disubstituted<\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Bottom: Mass Spectrum<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Base peak at m\/z = 105<\/strong>: Benzoyl fragment (C\u2086H\u2085\u2013CO\u207a)<\/li>\n\n\n\n<li><strong>Molecular ion peak (M\u207a) at m\/z = 140<\/strong>, matches <strong>C\u2088H\u2081\u2082O\u2082<\/strong><\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">3. <strong>Proposed Structure:<\/strong><\/h3>\n\n\n\n<p><strong>Ethyl 4-hydroxybenzoate<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Benzene ring with OH at para position to an ester<\/li>\n\n\n\n<li>Explains IHD (aromatic ring = 4, minus symmetry)<\/li>\n\n\n\n<li>IR: C=O and O\u2013H<\/li>\n\n\n\n<li>NMR: Aromatic 4H, ethyl group, OH (broad singlet)<\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">\u2705 Final Answer:<\/h3>\n\n\n\n<p><strong>Structure: Ethyl 4-hydroxybenzoate<\/strong><\/p>\n\n\n\n<p>(Structure would include a benzene ring with a hydroxyl group at the para position and an ethyl ester at the opposite para position)<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/learnexams.com\/blog\/wp-content\/uploads\/2025\/05\/learnexams-banner7-155.jpeg\" alt=\"\" class=\"wp-image-222311\"\/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>1E. CH1202 3000 2000 1000 4. PUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUUU 2.0 3. Wwwpo W Stand Wh Ards In Their Teatro LL 100 For Each Do The Following: Calculate The Index Of Hydrogen Deficiency (IHD), Label Each Spectra As The TYPE Of Spectra It Is, Label The Significant Peaks In Each Spectra, Determine The Structure And Draw A Box [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[25],"tags":[],"class_list":["post-222309","post","type-post","status-publish","format-standard","hentry","category-exams-certification"],"_links":{"self":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts\/222309","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/comments?post=222309"}],"version-history":[{"count":0,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts\/222309\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/media?parent=222309"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/categories?post=222309"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/tags?post=222309"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}