[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"detail-sidebar-cat-0-en-105":3,"doc-seo-331756-105":59,"doc-detail-331756-en":131},{"code":4,"msg":5,"data":6},0,"success",[7,13,18,23,28,33,38,43,48,51,55],{"id":8,"doc_module":4,"doc_module_name":9,"category_name":10,"show_sort_weight":11,"slug":12},1,"Document","Story & Novel",90,"story-novel",{"id":14,"doc_module":4,"doc_module_name":9,"category_name":15,"show_sort_weight":16,"slug":17},2,"Literature",80,"literature",{"id":19,"doc_module":4,"doc_module_name":9,"category_name":20,"show_sort_weight":21,"slug":22},4,"Exam",70,"exam",{"id":24,"doc_module":4,"doc_module_name":9,"category_name":25,"show_sort_weight":26,"slug":27},5,"Comic",60,"comic",{"id":29,"doc_module":4,"doc_module_name":9,"category_name":30,"show_sort_weight":31,"slug":32},6,"Technology",50,"technology",{"id":34,"doc_module":4,"doc_module_name":9,"category_name":35,"show_sort_weight":36,"slug":37},7,"Healthcare",40,"healthcare",{"id":39,"doc_module":4,"doc_module_name":9,"category_name":40,"show_sort_weight":41,"slug":42},8,"Research & Report",30,"research-report",{"id":44,"doc_module":4,"doc_module_name":9,"category_name":45,"show_sort_weight":46,"slug":47},9,"Religion & Spirituality",20,"religion-spirituality",{"id":46,"doc_module":4,"doc_module_name":9,"category_name":49,"show_sort_weight":46,"slug":50},"World Cup","world-cup",{"id":52,"doc_module":4,"doc_module_name":9,"category_name":53,"show_sort_weight":52,"slug":54},10,"Lifestyle","lifestyle",{"id":56,"doc_module":4,"doc_module_name":9,"category_name":57,"show_sort_weight":24,"slug":58},19,"General","general",{"code":4,"msg":60,"data":61},"ok",{"site_id":62,"language":63,"slug":64,"title":65,"keywords":66,"description":67,"schema_data":68,"social_meta":124,"head_meta":126,"extra_data":128,"updated_unix":130},105,"en","organic-chemistry-full-year-practice-items","Organic Chemistry - Full-Year Practice Items","","A year-long organic chemistry practice set structured by chapter concepts, focusing on mastery of bonding and hybridization, molecular structure and isomer identification via IUPAC naming, conformational stability in cyclohexane systems, and acidity/basicity ranking. It includes mechanistic and reactivity questions spanning SN1 kinetics, elimination outcomes, addition mechanisms across alkenes/alkynes and alcohol/ether transformations, and radical reaction reagent selection. Spectroscopy and electronics are tested through NMR signal interpretation and carbon counting, HOMO determination for conjugated systems, and aromaticity and Lewis acidity comparisons under kinetic control.",{"@graph":69,"@context":123},[70,84,106],{"@type":71,"itemListElement":72},"BreadcrumbList",[73,77,79,82],{"item":74,"name":75,"@type":76,"position":8},"https://docshare.wps.com","Home","ListItem",{"item":78,"name":9,"@type":76,"position":14},"https://docshare.wps.com/document/",{"item":80,"name":20,"@type":76,"position":81},"https://docshare.wps.com/document/exam/",3,{"item":83,"name":65,"@type":76,"position":19},"https://docshare.wps.com/document/organic-chemistry-full-year-practice-items/331756/",{"url":83,"name":65,"@type":85,"image":86,"author":91,"headline":65,"publisher":94,"fileFormat":97,"inLanguage":63,"description":67,"dateModified":98,"datePublished":99,"encodingFormat":97,"isAccessibleForFree":100,"interactionStatistic":101},"DigitalDocument",{"url":87,"@type":88,"width":89,"height":90},"https://docshare.wps.com/thumbnails/organic-chemistry-full-year-practice-items/331756.png","ImageObject",300,407,{"name":92,"@type":93},"Jordan Avery","Person",{"url":74,"name":95,"@type":96},"DocShare","Organization","application/pdf","2026-10-21","2026-09-21",true,{"@type":102,"interactionType":103,"userInteractionCount":105},"InteractionCounter",{"@type":104},"ViewAction",18,{"@type":107,"mainEntity":108},"FAQPage",[109,115,119],{"name":110,"@type":111,"acceptedAnswer":112},"What does the practice set cover across the year?","Question",{"text":113,"@type":114},"It covers core organic chemistry topics by chapter, including structure and stability, isomer identification, acids and bases, substitution and elimination, addition reactions, radical reactions, spectroscopy interpretation, and conjugated/aromaticity fundamentals.","Answer",{"name":116,"@type":111,"acceptedAnswer":117},"How are the questions organized within each chapter?",{"text":118,"@type":114},"Each chapter includes multiple study and practice questions labeled with section letters (e.g., 1A, 1B) and often includes work space and answer choices.",{"name":120,"@type":111,"acceptedAnswer":121},"What kinds of skills are tested in the spectroscopy and reactivity questions?",{"text":122,"@type":114},"Spectroscopy questions test NMR understanding such as chemical shift features and counting distinct signals, while reactivity questions test mechanisms and outcomes such as SN1 speed trends, elimination major products, reagent selection, and kinetic versus thermodynamic product control.","https://schema.org",{"og:url":83,"og:type":125,"og:title":65,"og:site_name":95,"og:description":67},"article",{"robots":127,"canonical":83},"index,follow",{"doc_id":129,"site_id":62},331756,1790177512,{"code":4,"msg":5,"data":132},{"doc_id":129,"user_id":133,"nickname":92,"user_avatar":134,"doc_module":4,"category_id":19,"category_name":20,"doc_title":65,"doc_description":67,"doc_content":135,"file_id":136,"file_url":137,"file_type":138,"file_size":139,"view_count":105,"is_deleted":4,"is_public":8,"is_downloadable":8,"audit_status":8,"page_count":140,"language":141,"language_code":63,"site_id":62,"html_lang":63,"table_of_contents":142,"faqs":143,"seo_title":144,"seo_description":67,"update_tm":145,"read_time":146,"preview_page_count":4},1099523882367,"https://ap-avatar.wpscdn.com/davatar_9964176cb1d06d4a9deccf72a44ae3dc","Organic Chemistry, Full-Year Practice Items  \nStudy Question – Chapter 1 (Structure: Shape and Stability)  \n1A. What hybrid orbitals are used to form the sigma bond between the indicated carbon atoms (indicated with stars)?  \n* *  \n(A) sp and sp  \n(B) sp3 and sp  \n(C) sp2 and sp  \n(D) sp2 and sp3  \nWork:  \nPractice Question – Chapter 1 (Structure: Shape and Stability)  \n1B. Which of the following structures contributes more to the hybrid structure for this  \nmolecule?  \nO N H  \nO  \n(A) (B)  \nN H  \nN H  \nO  \n(C)    \nNH  \n(D)  \nWork:  \nReferences below are to the ACS Exams Organic Chemistry Study Guide For more practice, please see: Study Questions: SQ 6 and 10 (p. 20-23)  \nPractice Questions: PQ 11-16, 25-26 (p. 25-29)  \nStudy Question – Chapter 3 (Structure: Isomers) 2A. What is the IUPAC name of this molecule?  \nCl OH  \n(A) (2S, 4S) 2-chloro-5-ethylheptan-4-ol  \n(C) (2R, 4S) 2-chloro-5-ethylheptan-4-ol  \nWork:  \n(B) (2S, 4R) 2-chloro-5-ethylheptan-4-ol  \n(D) (2R, 4R) 2-chloro-5-ethylheptan-4-ol  \nPractice Question – Chapter 3 (Structure: Isomers)  \n2B. Which best describes the most stable conformation of cis-1-chloro-4-isopropylcyclohexane?  \n(A) The isopropyl group is equatorial, and the chloro group is axial.  \n(B) The isoprpyl group is axial, and the chloro group is equatorial.  \n(C) Both the chloro and isopropyl group are equatorial.  \n(D) Both the chloro and isopropyl group are axial.  \nWork:  \nFor more practice, please see: Study Questions: SQ1, 4 (p. 41-45)  \nPractice Questions: PQ1-5, 11-14 (p. 48-50)  \nStudy Question – Chapter 4 (Acids and Bases)  \n3A. Rank the following compounds in order of increasing acidity.  \nO  \nOH  \nO2 N  \nOH  \nO2 N  \nO  \nOH  \nOH  \nI II III IV  \n(A) II \u003C IV \u003C I \u003C III (B) II \u003C IV \u003C III \u003C I (C) IV \u003C III \u003C II \u003C I (D) IV \u003C II \u003C I \u003C III  \nWork:  \nPractice Question – Chapter 4 (Acids and Bases)  \n3B. What is the most basic nitrogen lone pair in the molecule below?  \n(A) I (B) II (C) III (D) IV  \nWork:  \nFor more practice, please see: Study Questions: SQ 7-8 (p.59-60)  \nPractice Questions: PQ 22-27 (p.63-64)  \nStudy Question – Chapter 5 (Nucleophilic Substitution Reactions) 4A. Which compound would react the fastest in an SN 1 reaction?  \nWork:  \nPractice Question – Chapter 6 (Elimination Reactions) 4B. What is the major product of the following reaction?  \nWork:  \nFor more practice, please see: Study Questions: Ch 5 SQ-5, Ch 6 SQ-3(p.70, 80-81)  \nPractice Questions: Ch 5 PQ 13-18, Ch 6 PQ 3-8 (p.75-76, 86-87)  \nStudy Question – Chapter 7 (Addition Reactions: Alkenes and Alkynes) 5A. Which reaction step occurs in this reaction mechanism?  \nOH  \n(A)  \n(C)  \nWork:  \n(B)  \n(D)  \nOH2  \nPractice Question – Chapter 7 (Addition Reactions: Alkenes and Alkynes)  \n5B. What is the major product of the following reaction?  \n1) BH3/THF   \n- 2) H2O2 , OH  \n(A)  \nOH  \n(B)  \nBH2  \n(C)  \nOH  \nWork:  \nO  \n(D) H  \nFor more practice, please see: Study Questions: SQ 4, 7 (p.96-98)  \nPractice Questions: PQ 12-14, 18-19 (p. 103-105)  \nStudy Question – Chapter 8 (Addition Reactions: Alcohols and Ethers)  \n6A. What is the best reagent(s) to bring about the following transformation?  \nO  \nOH  \nOH  \n(A) PCC, CH2Cl2 (B) LiAlH4, H3O+ (C) K2Cr2O7, NaOH (D) mCPBA  \nWork:  \nPractice Question – Chapter 8 (Addition Reactions: Alcohols and Ethers)  \n6B. Which reagents would yield this product in the highest yield?  O  \n(A)  \nOH  \n1) NaH  (B)  \n2) CH3Br  \n1) Hg(OAc)2 , CH3OH -  \n2) NaBH4 , OH  \n(C)  \nCH3OH  \n+  (D)  \nH  \nCl  \nCH3ONa  \nWork:  \nFor more practice, please see: Study Questions: SQ 3, 7 (p.111-113)  \nPractice Questions: PQ 5-9, 18-20 (p. 115-120)  \nStudy Question – Chapter 9 (Spectroscopy)  \n7A. Which of the following hydrogen(s) would best account for a doublet in the 1 H NMR spectra at a chemical shift of 0.8 ppm?  \n(A) Ha (B) Hb (C) Hc (D) Hd  \nWork:  \nPractice Question – Chapter 9 (Spectroscopy)  \n7B. How many chemically distinct carbon signals are present in an NMR of 4-methylbenzaldehyde? O  \nH  \n(A) 5 (B) 6 (C) 7 (D) ","cbCaiir1U55ZWWRQ","https://ap.wps.com/l/cbCaiir1U55ZWWRQ","pdf",491773,15,"English","# Chapter 1 - Structure: Shape and Stability\n## 1A-1B\n# Chapter 3 - Structure: Isomers\n## 2A-2B\n# Chapter 4 - Acids and Bases\n## 3A-3B\n# Chapter 5 - Nucleophilic Substitution Reactions\n## 4A\n# Chapter 6 - Elimination Reactions\n## 4B\n# Chapter 7 - Addition Reactions: Alkenes and Alkynes\n## 5A-5B\n# Chapter 8 - Addition Reactions: Alcohols and Ethers\n## 6A-6B\n# Chapter 9 - Spectroscopy\n## 7A-7B\n# Chapter 10 - Radical Reactions\n## 8A-8B\n# Chapter 11 - Conjugated Systems & Aromaticity\n## 9A-10B","[{\"question\":\"What does the practice set cover across the year?\",\"answer\":\"It covers core organic chemistry topics by chapter, including structure and stability, isomer identification, acids and bases, substitution and elimination, addition reactions, radical reactions, spectroscopy interpretation, and conjugated/aromaticity fundamentals.\"},{\"question\":\"How are the questions organized within each chapter?\",\"answer\":\"Each chapter includes multiple study and practice questions labeled with section letters (e.g., 1A, 1B) and often includes work space and answer choices.\"},{\"question\":\"What kinds of skills are tested in the spectroscopy and reactivity questions?\",\"answer\":\"Spectroscopy questions test NMR understanding such as chemical shift features and counting distinct signals, while reactivity questions test mechanisms and outcomes such as SN1 speed trends, elimination major products, reagent selection, and kinetic versus thermodynamic product control.\"}]","Organic Chemistry - Full-Year Practice Items | PDF",1789994998,38]