北京化工大学:《有机化学》课程教学资源(模拟试卷)有机A期末试卷及其答案

Organic Chemistry Exam(A) Final Chinese Name: Student ID: Credit Question 1 2 3 5 Total Credits 1.Name the following compounds in English(IUPAC)or in Chinese(CCS)(20) ② IUPAC:(3.5S)-3.5-dimethyloctane IUPAC: a○oH 2R.5txame-5 ④入0 IUPAC:cydohexano IUPAC:1-propoxypropane ⑤)入今 〈口 IUPAC:(E)-2-hexene IUPAC:(Z)-2.5-dimethyIhex-3-ene 0 IUPAC:2-hexyne IUPAC:cis-1.3-dichlorocyclopentane ⑨)、个8 CCS:反式1甲基4-溴环己烷 d CCS:(R,风-1氯-3溴环戊烷 2.Answer the following questions(20) 3 (1)Identify which of the following compounds possess optical activity. b c EtOzC H d ZH HO-H eo HCOZEt HO-H O,H a:no b:optical activity c:optical activity d:no
1 Organic Chemistry Exam (A) Final Chinese Name: Student ID: Credit: Question 1 2 3 4 5 Total Credits _____________________________________________________________________ 1. Name the following compounds in English (IUPAC) or in Chinese (CCS) (20) (1) (2) Cl Br IUPAC: IUPAC: (3) (4) (5) (6) (7) (8) (9) (10) OH O IUPAC: IUPAC: IUPAC: IUPAC: Cl H Cl H IUPAC: IUPAC: Br CCS: 反式-1-甲基-4-溴环己烷 H Br Cl H CCS: (3S,5S)-3,5-dimethyloctane (2R,5R)-2-bromo-5- chlorohexane cyclohexanol 1-propoxypropane (E)-2-hexene (Z)-2,5-dimethylhex-3-ene 2-hexyne cis-1,3-dichlorocyclopentane (R,R)-1-氯-3-溴环戊烷 2. Answer the following questions (20) 3. (1) Identify which of the following compounds possess optical activity. H CO2Et EtO2C H Br Bu-t a b c d CO2H HO H CO2H HO H OH Br MeO a: no b: optical activity c: optical activity d: no

(2)Draw stable conformations for the following compounds b Ph Newmann Project =0 H-OH Me 大 人H Me ph (3)Put the following intermediates in indicated orders. 'QOx○c b MegC.CHg.Me2CH,CHgCHz Stability increasing order.CH3 CHaCH2,Me2CH,MeC. (4)Identify the stereochemical relationships of the following structures (identical,enantiomer,diastereomer). a Dh 6 4 a:Diastereomers b:identical 4.Predict major products for following reactions,and indicate the stereochemistry if optional.(30) 2
2 (2) Draw stable conformations for the following compounds Cl OH Me H Ph O a b Newmann Project Cl O Me H Ph O H (3) Put the following intermediates in indicated orders. a b CH2 + + + Stability increasing order: Me3C. , CH3 . , Me2CH. , CH3CH2 . Stability increasing order: CH2 + + + CH3 . , CH3CH2 . , Me2CH. , Me3C. , (4) Identify the stereochemical relationships of the following structures (identical, enantiomer, diastereomer). H Ph HO Ph H OH a b H Ph HO OH H Ph Cl H H Cl H Cl H Cl a: Diastereomers b: identical 4. Predict major products for following reactions, and indicate the stereochemistry if optional. (30)

(1) 2芯6oH H20,H OH ( 3)入入Br Mg.E0 入√入MgBr PhCH2CI HgO* 〈Ph OH 0s04,H202 OH ,() OH MCPBA- EtOH,H' CH2Cl2.Na2CO3 () 6) () 、TsC,Py OTs AcOK OA 8)Br.CC4 +
3 (1) (2) 1, B2H6, THF 2. H2O2, NaOH H2O, H+ (3) (4) (5) (6) (7) (8) Br Mg, Et2O PhCH2Cl H3O+ OsO4, H2O2 MCPBA CH2Cl2, Na2CO3 EtOH, H+ OH TsCl, Py AcOK Br EtONa Br2, CCl4 OH OH MgBr Ph (+) OH OH (+) O (+) OH O (+) OTs OAc Br Br (+)

(12) 人=一/2:品N0 ) PCC.CHzCl2 人人0 00 (+) 5.Write stepwise and reasonable mechanisms for the following reactions (20). 0今cH+ch500℃ c1-C150c、2G 今H+c→入·+c 入·+ck→入+ 2CF CI-CI 2入·→入入 今·+c→今d
4 (9) (10) (11) (12) (13) (14) (15) O O O + High T 1. Na, NH3 (l) 2. EtOH OH PCC, CH2Cl2 HgSO4, H2O, H2SO4 O Br2, hv O O O H H (+) O O O Br (+) 5. Write stepwise and reasonable mechanisms for the following reactions (20). CH3 + Cl2 500 oC (1) Cl Cl Cl 500o C 2 Cl. H + Cl. + HCl + Cl2 Cl + Cl. 2 Cl Cl Cl . + Cl. Cl 2

◇6·公 +) 。 cr.-c.c maio ④入+ESNa 人+EsNa SE 6.Synthesize the following organic compounds with provided starting materials and necessary inorganic reagents.(10)[*Note:(3)is additional question with 5 point bonus] Starting materials:Toluene (MeCH).NBS,I-chorobutane and no more than4 carbon atoms organic compounds
5 OH + HBr Br (+) (2) OH + HBr Br (+) OH2 + -H2O + + Br- -Br- + HBr + Br major Br minor (3) Br H+ + BrBr + EtSNa (4) SEt Br + EtSNa Br SEt S SN2 6. Synthesize the following organic compounds with provided starting materials and necessary inorganic reagents. (10) [*Note: (3) is additional question with 5 point bonus] Starting materials: Toluene (MeC6H5), NBS, 1-chlorobutane and no more than 4 carbon atoms organic compounds. O (1) (2) (3)* O

”① 6
6 O O (1) (2) (3)* NBS, CCl4 Br OH ONa NaOH NaNH2 BuBr H2, Lindlar catalyst NaNH2 BuBr HgSO4, H2O, H2SO4
按次数下载不扣除下载券;
注册用户24小时内重复下载只扣除一次;
顺序:VIP每日次数-->可用次数-->下载券;
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机B期中试卷及其答案.pdf
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机B期中试卷.pdf
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机A期末试卷.pdf
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机A期中试卷及其答案.pdf
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机A期中试卷.pdf
- 《有机化学》课程教学资源(文献资料)[3,3]σ迁移反应过渡态立体化学过程的新观点.pdf
- 《有机化学》课程教学资源(文献资料)芳香过渡态理论及其在协同反应中的应用.pdf
- 《有机化学》课程教学资源(文献资料)芳香性概念的新发展.pdf
- 《有机化学》课程教学资源(文献资料)对映体识别_不对称合成中的新概念.pdf
- 《有机化学》课程教学资源(文献资料)多环体系的芳香性.pdf
- 《有机化学》课程教学资源(文献资料)多烯化合物的Cope重排反应——[5,5]σ迁移、串联[3,3]σ迁移与自由基重排机理.pdf
- 《有机化学》课程教学资源(文献资料)E2反应中的反式共平面构象.pdf
- 《有机化学》课程教学资源(文献资料)各类手性质子源及其在去消旋化反应中的应用.pdf
- 《有机化学》课程教学资源(文献资料)分子内氢键对化合物性质的影响.pdf
- 《有机化学》课程教学资源(文献资料)共轭效应和芳香性本质的争论和它们的历史发展.pdf
- 《有机化学》课程教学资源(文献资料)含手性碳原子的[3,3]σ迁移反应的立体化学过程.pdf
- 《有机化学》课程教学资源(文献资料)关于芳香性的概念.pdf
- 《有机化学》课程教学资源(文献资料)关于不对称合成反应中若干问题的讨论.pdf
- 《有机化学》课程教学资源(文献资料)试剂的亲核性和碱性.pdf
- 《有机化学》课程教学资源(文献资料)同芳香性探析.pdf
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机B期末试卷及其答案.pdf
- 北京化工大学:《有机化学》课程教学资源(模拟试卷)有机B期末试题.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 01 Structure and Bonding in Organic Molecules.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 02 Structure and Reactivity:Acids and Bases, Polar and Nonpolar Molecules.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 03 Reactions of Alkanes:Bond-Dissociation Energies, Radical Halogenation, and Relative Reactivity.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 04 Cycloalkanes.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 05 Stereoisomers.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 06 Properties and Reactions of Haloalkanes - Bimolecular Nucleophilic Substitution.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 07 Further Reactions of Haloalkanes:Unimolecular Substitution and Pathways of Elimination.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 08 Hydroxy Functional Group:Alcohols:Properties, Preparation, and Strategy of Synthesis.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 09 Further Reactions of Alcohols and the Chemistry of Ethers.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 10 Using Nuclear Magnetic Resonance Spectroscopy to Deduce Structure.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 11 Alkenes; Infrared Spectroscopy and Mass Spectrometry.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 12 Reactions of Alkenes.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 13 Alkynes:The Carbon–Carbon Triple Bond.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 14 Delocalized Pi Systems:Investigation by Ultraviolet and Visible Spectroscopy.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 15 Benzene and Aromaticity:Electrophilic Aromatic Substitution.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 16 Electrophilic Attack on Derivatives of Benzene:Substituents Control Regioselectivity.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 17 Aldehydes and Ketones:The Carbonyl Group.pdf
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 18 Enols, Enolates, and the Aldol Condensation:a, b-Unsaturated Aldehydes and Ketones.pdf