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

1.What would be the product of the following reaction? Pge】
Page 1 1. What would be the product of the following reaction? O CH3 H CH3OH H+ ? A) OH CH3 H OCH3 B) H OH CH3O CH3 C) OH H CH3O CH3 D) H OH H3C OCH3 E) OH H CH2 Ans: A

2.What would be the product of the following reaction? 25℃ CH3CH2OCH2CH3 2 (slow) CO+BO CH3-CH-O-CH2-CH3 OOH C)CH:-CH2-0-CH2-CH2-OOH D)CH-CH2-O-O-CH2-CH3 E)CH;-CH2-O-CH2-CH2OH Ans:B Ot ing would you)coiline points would CH:OCH: Ans:C 4.What reagent would best accomplish the following reaction? CH2CH2OH B)NaBr C)CH;Br D)NH,*Br E)PBr Page2
Page 2 2. What would be the product of the following reaction? A) CO2 + H2O B) OOH CH3 CH O CH2 CH3 C) CH3 CH2 O CH2 CH2 OOH D) CH3 CH2 O O CH2 CH3 E) CH3 CH2 O CH2 CH2OH Ans: B 3. Which of the following would you expect to have the lowest boiling point? A) CH3CH2OH D) CH3SCH3 B) CH3CH2SH E) boiling points would be the same. C) CH3OCH3 Ans: C 4. What reagent would best accomplish the following reaction? CH2CH2OH CH2CH2Br ? A) Br2 B) NaBr C) CH3Br D) NH4 + Br- E) PBr3 Ans: E

5.What would be the expected product of the following reaction? Page 3
Page 3 5. What would be the expected product of the following reaction? SH + I2 ? A) S S B) I C) (trans) D) (cis) E) O S O OH Ans: A

6.What would be the expected product(s)of the following reaction? HI(excess) CHCH2CH2CH2-O-CH2CH2CH2CH3 heat CHCH-CH-CH.OH CH.CH.CHCH CH;CH2CH2CHI-O-CH2CH2CH2CH3 8 2 CH;CH-CH-CH2I CH;CH2CH2CH2-Q-CH2CH2CH2CH; Page4
Page 4 6. What would be the expected product(s) of the following reaction? CH3CH2CH2CH2 O CH2CH2CH2CH3 ? HI (excess) heat A) CH3CH2CH2CH2OH + CH3CH2CH2CH2I B) CH3CH2CH2CHI-O-CH2CH2CH2CH3 C) 2 CH3CH2CH2CH2I D) CH3CH2CH2CH2 O CH2CH2CH2CH3 H + IE) no reaction occurs Ans: C

7.What would be the major organic product from the following reaction? H马OH HCI(cone) CH;- H.C CH ,CH3 H CH CH3- H;C CH HH CI (racemic) H.C CH -CH H H c二 H:C CH Ans:D Page5
Page 5 7. What would be the major organic product from the following reaction? H CH3 C H3C C OH CH3 H ? HCl (conc) A) H CH3 C H3C C Cl CH3 H B) H CH3 C H3C C H CH3 Cl C) H CH3 C H3C C Cl CH3 H (racemic) D) Cl CH3 C H3C C H CH3 H E) C H3C H3C C CH3 H Ans: D

8.What would be the best name of the following compound? 2-buto yethane 2-ethoxybutane 1-methy-1-ethoxypropane Ans:E 9 unctio as an anes ble It can react slowly with oxygen at room temperature. E)All of the above are true. Ans:E Page6
Page 6 8. What would be the best name of the following compound? O A) 3-methyl-4-oxohexane D) (1-ethyl)-diethylether B) 2-butoxyethane E) 2-ethoxybutane C) 1-methy-1-ethoxypropane Ans: E 9. What significant characteristic(s) does diethyl ether exhibit? A) It functions as an anesthetic. B) It is extremely flammable. C) It is a common solvent. D) It can react slowly with oxygen at room temperature. E) All of the above are true. Ans: E

10.Which of the following reactions would be the best for the preparation of anisole (methoxybenzene) O-CH3 on con H2SO 1.CH3MgBr 2H0+ one of the Page7
Page 7 10. Which of the following reactions would be the best for the preparation of anisole (methoxybenzene)? O CH3 A) Br ? CH3O- Na+ B) OH ? CH3OH H2SO4 C) O- Na+ ? CH3Br D) O ? 1. CH3MgBr 2. H3O+ E) None of the above would work. Ans: C

11.Which of the following reactions would be best for the preparation of Nerolin II c O-CH2CH3 Nerolin II (odor of orange blossoms) on angna H2S04 os CICIE DMSO CH;CH2O Na* DMSO D Ans:B ncombustion nu The nroducts can tration E) By absorbing all of the oxygen in closed areas,ethers pose suffocation risks Ans: Page8
Page 8 11. Which of the following reactions would be best for the preparation of Nerolin II? O CH2CH3 Nerolin II (odor of orange blossoms) A) OH ? CH3CH2OH H2SO4 B) O- Na+ ? CH3CH2Br DMSO C) Br CH3CH2O- Na+ DMSO ? D) Any of the above would work. E) None of the above would work. Ans: B 12. Why is the autoxidation (slow oxidation by air) of ethers important? A) Several industrial chemicals are made by this method. B) The heat generated often leads to open combustion. C) It makes ethers unusable as anesthetics. D) The products can explode upon concentration. E) By absorbing all of the oxygen in closed areas, ethers pose suffocation risks. Ans: D

13.What would be the product of the following reaction? CH3S"K' Page9
Page 9 13. What would be the product of the following reaction? O H H ? CH3S- K+ A) H OH H SCH3 B) OH H3CS H H C) H OH H SCH3 D) OSCH3 H H H E) H OH Ans: A

14.What product would result from the following reaction 9 HBr (exces) Page 10
Page 10 14. What product would result from the following reaction? O ? HBr (excess) heat A) O Br B) OH Br C) O Br D) Br OH E) Br Br Ans: B
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(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 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 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 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 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 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 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 01 Structure and Bonding in Organic Molecules.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(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A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
- 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
- 北京化工大学:《有机化学》课程教学资源(章节测验,含答案)Chapter 19 Carboxylic Acids.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 20 Carboxylic Acid Derivatives.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 21 Amines and Their Derivatives:Functional Groups Containing Nitrogen.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 22 Chemistry of Benzene Substituents:Alkylbenzenes, Phenols, and Benzenamines.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 23 Ester Enolates and the Claisen Condensation:Synthesis of b-Dicarbonyl Compounds; Acyl Anion Equivalents.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 24 Carbohydrates:Polyfunctional Compounds in Nature.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 25 Heterocycles:Heteroatoms in Cyclic Organic Compounds.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 26 Amino Acids, Peptides, Proteins, and Nucleic Acids:Nitrogen-Containing Polymers in Nature.pdf
- 北京化工大学:《有机化学》课程教学资源(习题与答案)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(习题与答案)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(习题与答案)Chapter 03 Reactions of Alkanes:Bond-Dissociation Energies, Radical Halogenation, and Relative Reactivity.pdf