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It lists Test 2 (four versions), Test 3 (three versions), Test 4 (three versions), and a Final Exam, with page references for each.","https://schema.org",{"og:url":32,"og:type":75,"og:title":10,"og:site_name":45,"og:description":12},"article",{"robots":77,"canonical":32},"index,follow",{"doc_id":79,"site_id":7},331731,1790195671,{"code":4,"msg":82,"data":83},"success",[84,88,92,95,100,104,109,114,119,122,126],{"id":22,"doc_module":4,"doc_module_name":25,"category_name":85,"show_sort_weight":86,"slug":87},"Story & Novel",90,"story-novel",{"id":26,"doc_module":4,"doc_module_name":25,"category_name":89,"show_sort_weight":90,"slug":91},"Literature",80,"literature",{"id":33,"doc_module":4,"doc_module_name":25,"category_name":29,"show_sort_weight":93,"slug":94},70,"exam",{"id":96,"doc_module":4,"doc_module_name":25,"category_name":97,"show_sort_weight":98,"slug":99},5,"Comic",60,"comic",{"id":55,"doc_module":4,"doc_module_name":25,"category_name":101,"show_sort_weight":102,"slug":103},"Technology",50,"technology",{"id":105,"doc_module":4,"doc_module_name":25,"category_name":106,"show_sort_weight":107,"slug":108},7,"Healthcare",40,"healthcare",{"id":110,"doc_module":4,"doc_module_name":25,"category_name":111,"show_sort_weight":112,"slug":113},8,"Research & Report",30,"research-report",{"id":115,"doc_module":4,"doc_module_name":25,"category_name":116,"show_sort_weight":117,"slug":118},9,"Religion & Spirituality",20,"religion-spirituality",{"id":117,"doc_module":4,"doc_module_name":25,"category_name":120,"show_sort_weight":117,"slug":121},"World Cup","world-cup",{"id":123,"doc_module":4,"doc_module_name":25,"category_name":124,"show_sort_weight":123,"slug":125},10,"Lifestyle","lifestyle",{"id":127,"doc_module":4,"doc_module_name":25,"category_name":128,"show_sort_weight":96,"slug":129},19,"General","general",{"code":4,"msg":82,"data":131},{"doc_id":79,"user_id":132,"nickname":42,"user_avatar":133,"doc_module":4,"category_id":33,"category_name":29,"doc_title":10,"doc_description":12,"doc_content":134,"file_id":135,"file_url":136,"file_type":137,"file_size":138,"view_count":55,"is_deleted":4,"is_public":22,"is_downloadable":22,"audit_status":22,"page_count":139,"language":140,"language_code":8,"site_id":7,"html_lang":8,"table_of_contents":141,"faqs":142,"seo_title":143,"seo_description":12,"update_tm":144,"read_time":145,"preview_page_count":4},549768064778,"https://ap-avatar.wpscdn.com/davatar_6f874abed73319feea01a86fa6f0fab8","1  \n# Practice Tests Answer Keys, Organic Chemistry 2\n\nOnline Organic Chemistry 2, Chem 360, Dr. Craig P. Jasperse, Minnesota State University MoorheadFor full class website, see  \nhttps://collaborate. mnstate.edu/public/blogs/jasperse/online-organic-chemistry-courses/online-organic-chemistry-ii-360-fall-spring/  \n\n| Test   | Page   |\n| --- | --- |\n| Test 1 Version 1   | 3   |\n| Test 1 Version 2   | 9   |\n| Test 1 Version 3   | 15   |\n| Test 1 Version 4   | 21   |\n| Test 2 Version 1   | 27   |\n| Test 2 Version 2   | 35   |\n| Test 2 Version 3   | 43   |\n| Test 2 Version 4   | 51   |\n| Test 3 Version 1   | 61   |\n| Test 3 Version 2   | 67   |\n| Test 3 Version 3   | 75   |\n| Test 4 Version 1   | 81   |\n| Test 4 Version 2   | 87   |\n| Test 4 Version 3   | 93   |\n| Final Exam   | 101   |\n\n2  \nTe  \n1  \nJASPERSE CHEM 360 TEST 1 VERSION 1  \nAlcohols and Retrosynthesis  \n## 1. Give the major product for the following reactions. (3 points each)\n\nO  \n  \n  \n1. MgBr  \n  \n2. H 3O+  \nH 2CrO4Ph OH   \n3  \nO  1. PhMgBr (excess)  \nOCH 3 +  \n2. H 3O  \nOH  \n  \n  \n  \nO  \nO  \nH OH  \n1. TsCl, pyridine  \n  \n2. NEt 3, heat  \n1. LiAlH 4  \n2. H 3O+  \n  \n1. Na  \n2. Br  \n1. PBr 3 3. PhCHOOH  2. Mg 4. H 3O+   \nTe  \n2  \n## 2. Give Names or structures for the following: (9 points)\n\npara-ethylphenol  \n4  \nOH  \nOH  \nCl  \n(E)-6-chlorohept-4-en-3-ol  \n3-methyl-3-propylpentan-1-ol  \n3. For each of the following pairs, circle the one that is higher boiling and put a square aroundthe one with the higher water solubility. (4 points)  \na. OH OH  \nHOOH H 3COH  \nb.    \n## 4. Which of the following statements is true? (4 points)\n\na. When an ether solution of A and B in a separatory funnel is treated with neutral water, only Bremains in the ether layer.  \nb. When an ether solution of A and B in a separatory funnel is treated with neutral water, neitherA nor B remains in the ether layer.  \nc. When an ether solution of A and B in a separatory funnel is treated with basic water(NaOH/H2O), both A and B remain in the ether layer.  \nd. When an ether solution of A and B in a separatory funnel is treated with basic water(NaOH/H2O), only B remains in the ether layer.  \nOH OH  \n  \n  \n  \n  \nA B  \n## 5. For the following transformation, which of the following statements is true? (4 points)\n\na. D is the only acceptable solventb. C is the only acceptable solventc. C and D are both acceptable solvents  \nd. B, C, and D are all acceptable solvents  \ne. A and B are the only acceptable solvents  \nBr  \n1. Mg, solvent  \n2. H 2C=O  \n3. H 3O+  \n  \nOH  \n| Solvent Options   |  |  |  |\n| --- | --- | --- | --- |\n| H 2O  \u003Cbr>A   | CH 3OH  \u003Cbr>B   | O  \u003Cbr>  \u003Cbr>  \u003Cbr>C   | O  \u003Cbr>D   |\n\nTe  \n3  \n6. Suggest a possible structure for an unknown A whose formula is C5H 10O and gives thefollowing chemical test results. (5 points)  \nFormulaHydrogenation TestChromic Acid TestLucas Test  \nC5H 10O  \nH2/Pt  \nH2CrO4HCl/ZnCl2  \nNo reaction  \nTurns Green  \nReacts within 5 minutes  \n## 7. Provide the mechanisms for the following reactons (3, 5, and 5 points)\n\nO  \n1. LiAlH 4  \n2. H 3O+  \n  \nOH  \n5  \nO  \n  \nCl  \n1. MeMgBr  \n2. H 3O+  \nOH  \n  \nMe  \nMe  \n(\"Me\"=methyl=CH3)  \nOH  \n  \n Me  \nMe  \nH-Br  \n  \nBr  \n  \nMeMe  \n4  \n##  8. Provide the reagents necessary to accomplish the following transformations (4 points each)\n\n6  \nTe  \nO O  \n      (2-3 steps)  \n Ph  \nO  \n  \nOCH3  \n  \nO  \nBr  \nOCH3  \n  \nO  \n(2-3 steps)  \nPhBr   PhPh (2-3 steps)Ph OH  \nOH  \nOH     (2-3 steps)  \nOH O  \n   (2 steps)  \noptically active optically active  \nO  \nPhOH  PhOH (4-5 steps)  \nTe  \n5  \n## 9. Rank the acidity of the following, from most acidic (1) to least acidic (4) . (4 points)OH H 2O OH \n\n  \n## 10. Design syntheses of the following. (6 points each) . Allowed starting materials (same aspractice) include:\n\ncyclopentanol any esters ethylene oxide formaldehyde iodomethaneany acyclic alcohol or alkene wth ≤4 carbons  \nany “inorganic” agents (things that won’t contribute carbons to your skeleton)  \n7  \nO  \n8  \n  \n  \nT  \n  \n  \nT   \n  \n  \nT   \n1  \n","cbCaimMNFmE92SEP","https://ap.wps.com/l/cbCaimMNFmE92SEP","pdf",68341688,109,"English","# Practice Tests Answer Keys, Organic Chemistry 2 - Chem 360\n## Test 1 (Version 1-4) \n## Test 2 (Version 1-4)\n## Test 3 (Version 1-3)\n## Test 4 (Version 1-3)\n## Final Exam","[{\"question\":\"What types of questions are included in the Organic Chemistry 2 (Chem 360) practice test answer keys?\",\"answer\":\"The answer keys cover major product predictions for reactions, naming/structure drawing, boiling point and water solubility comparisons, solvent and ether-layer partitioning questions, mechanism writing, reagent selection for transformations, and synthesis design problems.\"},{\"question\":\"How many versions of Test 1 are provided in the answer key?\",\"answer\":\"Test 1 includes four versions (Version 1, Version 2, Version 3, and Version 4), each mapped to specific pages.\"},{\"question\":\"Does the document include answers for exams beyond Test 1?\",\"answer\":\"Yes. It lists Test 2 (four versions), Test 3 (three versions), Test 4 (three versions), and a Final Exam, with page references for each.\"}]","Practice Tests Answer Keys - Organic Chemistry 2 - Chem 360 | PDF",1789994915,275]