{"id":933,"date":"2023-01-12T11:22:35","date_gmt":"2023-01-12T16:22:35","guid":{"rendered":"https:\/\/blog.richmond.edu\/chem205l\/?page_id=933"},"modified":"2023-04-05T13:55:26","modified_gmt":"2023-04-05T17:55:26","slug":"project-5b-s23","status":"publish","type":"page","link":"https:\/\/blog.richmond.edu\/chem205l\/project-5b-s23\/","title":{"rendered":"Project 5B &#8211; S23"},"content":{"rendered":"<p style=\"text-align: center;\"><span style=\"text-decoration: underline;\"><strong>Background<\/strong><\/span><\/p>\n<p style=\"text-align: left;\">In CHEM 206, you will learn a variety of different reactions. Many of these qualify as condensation reactions, in which two (or more) small molecules (i.e., \u201cmonomers\u201d) combine to form a larger molecule. In the process, a small molecule (usually water) is expelled (Figure 1).<\/p>\n<div id=\"attachment_934\" style=\"width: 701px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-934\" class=\"wp-image-934 size-full\" src=\"http:\/\/blog.richmond.edu\/chem205l\/files\/2023\/01\/Condensation-Rxn-e1673540254702.jpg\" alt=\"\" width=\"691\" height=\"165\" srcset=\"https:\/\/blog.richmond.edu\/chem205l\/files\/2023\/01\/Condensation-Rxn-e1673540254702.jpg 691w, https:\/\/blog.richmond.edu\/chem205l\/files\/2023\/01\/Condensation-Rxn-e1673540254702-300x72.jpg 300w\" sizes=\"auto, (max-width: 691px) 100vw, 691px\" \/><p id=\"caption-attachment-934\" class=\"wp-caption-text\">Figure 1. A generic condensation reaction.<\/p><\/div>\n<p>In this project, you will use the structure determination skills you learned this semester to determine the outcome of a condensation reaction between vanillin and benzocaine in the presence of acetic acid (Figure 2).<\/p>\n<div id=\"attachment_935\" style=\"width: 449px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-935\" class=\"size-full wp-image-935\" src=\"http:\/\/blog.richmond.edu\/chem205l\/files\/2023\/01\/Project-5B_Imine-Rxn.jpg\" alt=\"\" width=\"439\" height=\"111\" srcset=\"https:\/\/blog.richmond.edu\/chem205l\/files\/2023\/01\/Project-5B_Imine-Rxn.jpg 439w, https:\/\/blog.richmond.edu\/chem205l\/files\/2023\/01\/Project-5B_Imine-Rxn-300x76.jpg 300w\" sizes=\"auto, (max-width: 439px) 100vw, 439px\" \/><p id=\"caption-attachment-935\" class=\"wp-caption-text\">Figure 2. Project 5B reaction puzzle.<\/p><\/div>\n<p style=\"text-align: center;\"><span style=\"text-decoration: underline;\"><strong>Procedure<\/strong><\/span><\/p>\n<p>1. In a 150 mL beaker, combine 1.50 g vanillin and 1.70 g benzocaine.<\/p>\n<p>2. Add 0.5 mL glacial acetic acid to the mixture. You may measure this quantity using the markings on the plastic pipettes available in the lab.<\/p>\n<p>3. Use a microspatula to vigorously mix the components until you obtain a dry yellow powder (~5 minutes).<\/p>\n<p>4.<span style=\"color: #3366ff;\"> <a style=\"color: #3366ff;\" href=\"https:\/\/blog.richmond.edu\/chem205l\/transferring-solids\/\">Transfer the solid<\/a><\/span> product to a 125 mL Erlenmeyer flask.<\/p>\n<p>5. <span style=\"color: #3366ff;\"><a style=\"color: #3366ff;\" href=\"https:\/\/blog.richmond.edu\/chem205l\/recrystallization\/\">Recrystallize<\/a><\/span> the solid using a 9:1 isopropanol:hexane solvent mixture.<\/p>\n<p>6. Collect the recrystallized solid by <span style=\"color: #3366ff;\"><a style=\"color: #3366ff;\" href=\"https:\/\/blog.richmond.edu\/chem205l\/vacuum-filtration\/\">vacuum filtration<\/a><\/span>.<\/p>\n<p>7. Perform a second recrystallization to further purify the solid. Collect the product by vacuum filtration and allow it to dry on the funnel for at least 30 minutes.<\/p>\n<p>8. Determine the product yield and characterize it by melting point analysis, GC-MS, IR, and NMR.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Background In CHEM 206, you will learn a variety of different reactions. Many of these qualify as condensation reactions, in which two (or more) small molecules (i.e., \u201cmonomers\u201d) combine to form a larger molecule. In the process, a small molecule &hellip; <a href=\"https:\/\/blog.richmond.edu\/chem205l\/project-5b-s23\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":5206,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"coauthors":[175315],"class_list":["post-933","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/pages\/933","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/users\/5206"}],"replies":[{"embeddable":true,"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/comments?post=933"}],"version-history":[{"count":3,"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/pages\/933\/revisions"}],"predecessor-version":[{"id":964,"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/pages\/933\/revisions\/964"}],"wp:attachment":[{"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/media?parent=933"}],"wp:term":[{"taxonomy":"author","embeddable":true,"href":"https:\/\/blog.richmond.edu\/chem205l\/wp-json\/wp\/v2\/coauthors?post=933"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}