VI. VII. During the reaction of benzene with n-propyl chloride and aluminum chloride as catalyst, the electrophilic species undergoing reaction with benzene is: A. B. n-propyl carbocation tert-butyl carbocation iso-propyl carbocation sec-butyl carbocation C. D. E. iso-butyl carbocation The reaction of benzonitrile with chlorine in the presence of iron(III) chloride as a catalyst provides: o-chlorocyanobenzene p-chlorocyanobenzene mixture of o-and p-chlorocyanobenzene m-chlorocyanobenzene E. mixture of m-and o-chlorocyanobenzene VIII. The nitration reaction of acetophenone provides: o-nitroacetophenone p-nitroacetophenone mixture of o-and p-nitroacetophenone m-nitroacetophenone No reaction occurred IX. A. ARCRE B. C. D. ARCRE A. B. C. D. E. Conversion of benzene into m-bromoaniline is achieved with the following sets of reagents arranged in right order: A. B. C. bromnine and iron(III) bromide, nitric acid and sulfuric acid, tin, hydrochloric acid, heat nitric acid and sulfuric acid, bromine and iron(III) bromide, tin, hydrochloric acid, heat tin, hydrochloric acid, heat, nitric acid and sulfuric acid, bromine and iron(III)

VI. VII. During the reaction of benzene with n-propyl chloride and aluminum chloride as catalyst, the electrophilic species undergoing reaction with benzene is: A. B. n-propyl carbocation tert-butyl carbocation iso-propyl carbocation sec-butyl carbocation C. D. E. iso-butyl carbocation The reaction of benzonitrile with chlorine in the presence of iron(III) chloride as a catalyst provides: o-chlorocyanobenzene p-chlorocyanobenzene mixture of o-and p-chlorocyanobenzene m-chlorocyanobenzene E. mixture of m-and o-chlorocyanobenzene VIII. The nitration reaction of acetophenone provides: o-nitroacetophenone p-nitroacetophenone mixture of o-and p-nitroacetophenone m-nitroacetophenone No reaction occurred IX. A. ARCRE B. C. D. ARCRE A. B. C. D. E. Conversion of benzene into m-bromoaniline is achieved with the following sets of reagents arranged in right order: A. B. C. bromnine and iron(III) bromide, nitric acid and sulfuric acid, tin, hydrochloric acid, heat nitric acid and sulfuric acid, bromine and iron(III) bromide, tin, hydrochloric acid, heat tin, hydrochloric acid, heat, nitric acid and sulfuric acid, bromine and iron(III)

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Which of these gives mostly the meta product when treated with Br2 / Fe?
Show how the following compounds can be prepared from benzene: a. benzaldehyde c. 1-bromo-2-phenylethane e. aniline b. styrene d. 2-phenylethanol f. benzoic acid
a. b. d. 8. The following reagents/conditions are capable of selectively oxidizing a primary alcohol to an aldehyde a. Swern Oxidation, Jones Reagent (H₂CrO4), DIBAL-H, PCC b. Swern Oxidation, Jones Reagent (H₂CrO4), DIBAL-H c. Swen Oxidation, PCC d. Swern Oxidation, PCC, DIBAL-H H₂O+ 9. The acid-catalyzed hydrolysis of the epoxide drawn above will give a. A diol as a 50/50 mixture of enantiomers b. A diol as an enantiopure compound c. A diol as a meso compound d. No reaction 10. The reaction below is in equilibrium. Which of the following methods will help drive the reaction forward to form a near quantitative yield of products? Circle the entire answer and all answers that apply. OCH3 OCH₂ + H₂O + 2 CH₂OH Use a large excess of methanol Use a chiral reagent Distill off the water that is formed in the reaction Add a drying agent, such as sodium sulfate
13. In the reaction of an alkene with dichlorocarbene, the dichlorocarbene is the: Electrophile a. b. Lewis base c. Nucleophile d. Both, b and c
What is the first step in the general mechanism for electrophilic aromatic substitution? a. aromatic ring protonation b.loss of the electrophilic aromatic ring c. deprotonation of the aromatic ring d.addition of the electrophilic to the aromatic ring.
494 7. Chapter 16 What is the product of each of the following reactions? a. CH3CH₂CH₂ b. CH3CH₂ c. CH3CH₂ d. e. CH3 OH NHCH, + ملی NH 1. SOCI2 2. CH3CH₂CH₂OH H₂O CH3 + 1. HO™ 2. CH3CH₂CH₂Br 3. HC1, H₂O, A HCI A H₂O excess + CH3CH₂OH HCI
Predict the products (if any) of the reaction of each of the ff. reagents with benzoic acid. a. conc. HCl b. CH3OH
Match the reactions with their products below. HAI(OIBU)3 1. a.) CI 1.) NABH4 2. b.) H. 2.) H3O* 3. (CH3),CuLi c.) OH 4. CH3OH d.) EtgN 5. HN(CH3)2 e.) EtgN
What is the major organic product obtained from the following reaction? A. B. low li LOH OH C. D. OH you
a. 4. What is the major product of the following reaction? os a4.04.0x b. a. C. b. H₂SO4 heat C. d. 5. Which is the second most stable alkene? of, of of of. of ? d. e. not a.-d. e.
25. How many of the following molecules will undergo chlorination at a higher rate than benzene and will produce ortho/para-substituted products? H'os ZON а. One d. Four e. Five b. Two с. Three 1 '1'.
pls help with these multiple choice questions