KWANTLEN UNIVERSITY COLLEGE CHEMISTRY R10 Organic Chemistry I

Similar documents
Time: 3 hours (180 minutes) Marking Scheme For The Exam

Organic Chemistry 3540

Chemistry 233 Exam 3 (Green) The Periodic Table

OChem1 Old Exams. Chemistry 3719 Practice Exams

Homework - Review of Chem 2310

Name. Department of Chemistry SUNY/Oneonta. Chem Organic Chemistry I. Examination #3 - November 11, 2002 ANSWERS

CHEM 231 (Davis) Organic Chemistry FINAL EXAM May 15, YOUR NAME (Last, First, M.I.) DISCUSSION SECTION #53 (5 Points)

- NH2 or NH 3 H 2 O or CH 3 COO - BF 3 or F - I Br. or Br

Chem 3719 Example Exams. Chemistry 3719 Practice Exams

Chemistry 250B Final Exam Answer Key December 19, 2008

H C C C C H C H C C H OH. Cl H CH 3. Br CH 3. H Br H OH H 3 C. CHEMISTRY MIDTERM # 3 June 17, Name...

Name. Department of Chemistry SUNY/Oneonta. Chem Organic Chemistry I. Examination #3 - November 8, 2004 ANSWERS

Departmental Final Examination. Organic Chemistry I Caffein

CHEM 2312 practice final. Version - II

REVIEW PROBLEMS Key. 1. Draw a complete orbital picture for the molecule shown below. Is this molecule chiral? Explain. H H.

Chem 232. Problem Set 9. Question 1. D. J. Wardrop

H C C C C H C H C C H H. Cl H CH 3 O. Br CH 3 OH H 3 C. H Br H

Chem 2061 Final Exam. Fall Andy Aspaas, Instructor. Thursday, December 15, Instructions: Please print: Last name: First name:

California State Polytechnic University, Pomona Chem 315. Exam Points 1. Nomenclature (1) 30

Chem Final Examination August 7, 2004

1. What are the respective hybridizations of the atoms numbered 1 to 4 in this compound?

Columbia University 92CORG14.DOC CHEM S3443D Summer 1992 Professor Grace B. Borowitz Exam No. 4 July 2, 1992

Chem ORGANIC CHEMISTRY I

CHEM 232 Exam Two April 5, 2010

3. (4 pts) Provide structures for the following compounds: CH 3 C H H C C - Na + acetylene 1-penten-4-yne (R)-3-butyn-2-ol sodium acetylide

ON THE FIRST DAY OF CHRISTMAS DR. RUSSELL GAVE TO ME, ORGANIC CHEMISTRY... Thanks to Dr R for the title!

a) 1. O 3 2. (CH 3 ) 2 S

350 Organic Chemistry I Winona State University

Chemistry 201. MW 12:00pm 1:15pm Examination #2 August 15 th Bronco ID. Question Score Possible Points. 1 (12pts) 2 (24pts) 3 (25pts)

Chapter 10 Lecture Outline

Chemistry 233 Exam 3. The Periodic Table

CHEMISTRY MIDTERM # 3 March 31, The total number of points in this midterm is 100. The total exam time is 120 min (2 h). Good luck!

Organic Chemistry CHM 224

More Tutorial at

Test Date: 30th September, 2018 (Sunday) Venue: Lajpat Rai Bhawan, Sector 15-B, Chandigarh

CHEMISTRY 341. Final Exam Tuesday, December 16, Problem 1 15 pts Problem 9 8 pts. Problem 2 5 pts Problem pts

As time allows, additional practice questions for Exam 2 follow. This is an incomplete collection. Content & emphasis will vary.

Chapter 9:Nucleophiles & Substitution Reactions

CHEM 2311 HW1. COMPLETELY FILL THE BOXES IN DARK PENCIL, i.e.:, NOT or or STRUCTURE

CHEMISTRY MIDTERM # 2 October 27, The total number of points in this midterm is 100. The total exam time is 120 min (2 h). Good luck!

If Compound 2 (below) was used in the above reaction, how might things change? Name Page 1. I. (23 points)

HO HO. 1) BH 3 HCl. + enantiomer either one may be drawn 4. + enantiomer either one may be drawn 4 1) O 3

This reactivity makes alkenes an important class of organic compounds because they can be used to synthesize a wide variety of other compounds.

Chapter 8: Chemistry of Alkynes (C n H 2n-2 )

diene. If stereoisomeric mixtures form, indicate by drawing one and writing "+ enantiomer" and/or "+ diastereomer" in the box.

More tutorial at

Columbia University C99ORG12.DOC S3443D Summer 99 Professor Grace B. Borowitz Exam No. 2 June 14, 1999

2311A and B Practice Problems to help Prepare for Final from Previous Marder Exams.

CHEM J-10 June The structure of ( )-linalool, a commonly occurring natural product, is shown below.

CH Organic Chemistry I (Katz) Practice Exam #3- Fall 2013

1. Name the following compound. Use the IUPAC system and include the stereochemical designations.

1. What are the respective hybridizations of the atoms numbered 1 to 4 in this compound?

Chapter 9. Nucleophilic Substitution and ß-Elimination

tbuo OtBu Br 1) B 2 H 6 /THF OH 2) OH - + H 2 O 2 NaNH 2 NH3 Na NH 3 /-35 C CH 3 CCH 2 CHCH 3

You must have your answers written in PERMANENT ink if you want a regrade!!!! This means no test written in pencil or ERASABLE INK will be regraded.

2 h; 240 points Signature UM ID # Problem Points Score GSI I 42 II 45 III 35 IV 46 V 36 VI 36 Total 240

CHEM120 - ORGANIC CHEMISTRY WORKSHEET 1

Lecture Notes Chem 51B S. King I. Conjugation

Stereochemistry is EZ! Thanks to Jonah H. for the title.

2/26/18. Practice Questions. Practice Questions B F. How many steps are there in this reaction?

Points: 1 / 15 / Total: 100 points /

Final Exam December 13, 2005 Professor Rebecca Hoenigman

CHEM 341: Organic Chemistry I at North Dakota State University Midterm Exam 02 - Fri, Mar 9, 2012!! Name:!

Chemistry 3351 Organic Chemistry/Final Exam Monday: Dec. 17 th from 1:30 pm 4:00pm

Chem 251 Fall Learning Objectives

Chemistry 210 Organic Chemistry I Winter Semester 2001 Dr. Rainer Glaser

Synthesis and Retrosynthesis

C h a p t e r S e v e n : Haloalkanes: Nucleophilc Substitution and Elimination Reactions S N 2

Chapter 7 Substitution Reactions 7.1 Introduction to Substitution Reactions Substitution Reactions: two reactants exchange parts to give new products

Chemistry 3719, Fall 2012 Exam 1 Name: Student number:

Homework - Review of Chem 2310

Problem Points Score GSI I 30 II 21 III 28 IV 30 V 31 Total 140

O N N. electrons in ring

Organic Chemistry CHM 314 Dr. Laurie S. Starkey, Cal Poly Pomona Alkyl Halides: Substitution Reactions - Chapter 6 (Wade)

Organic Chemistry I (Chem340), Spring Final Exam

Homework problems Chapters 6 and Give the curved-arrow formalism for the following reaction: CH 3 OH + H 2 C CH +

Practice Multiple-Choice Questions for Ending Chem 21 and/or Starting Chem 22

CHEM 241 CHIRALITY CHAP 4 ASSIGN

Chapter 7 Cyclic Compounds. Stereochemistry of Reactions

THE UNIVERSITY OF CALGARY FACULTY OF SCIENCE FINAL EXAMINATION CHEMISTRY 351 READ ALL THE INSTRUCTIONS CAREFULLY

Chemistry 210 Organic Chemistry I Fall Semester 2000 Dr. Rainer Glaser

Homework Problem Set 7 Iverson CH320M/328M Due Friday, Nov. 2

Organic Chemistry I Lesson Objectives, Lesson Problems, Course Outline Spring 2008

!!!! Organic Chemistry CHM 224. Exam I Questions

Chapter 11: Nucleophilic Substitution and Elimination Walden Inversion

CHEM 203. Midterm Exam 1 October 31, 2008 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

OChem 1 Mechanism Flashcards. Dr. Peter Norris, 2018

UCF - ORGANIC CHEMISTRY 1 - PROF. DAOUDI UCF PROF. DAOUDI EXAM 3 REVIEW.

OChem 1 Mechanism Flashcards. Dr. Peter Norris, 2015

OChem1 Course Pack Practice Exams Practice Problems by Chapter Mechanism Flashcards

FOURTH EXAMINATION. (1)..20 pts... (2)..24 pts... (3)..18 pts... (4)..12 pts... (5)..12 pts... (6).. 6 pts... (7).. 8 pts... Bonus 4 pts...

CHEM 261 HOME WORK Lecture Topics: MODULE 1: The Basics: Bonding and Molecular Structure Text Sections (N0 1.9, 9-11) Homework: Chapter 1:

CHEM 203. Final Exam December 15, 2010 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

CHEM 203. Final Exam December 16, This a closed-notes, closed-book exam. You may use your set of molecular models

Exam 3 November 17, 2005 Professor Rebecca Hoenigman

Note: You must have your answers written in pen if you want a regrade!!!!

3-chloro-1-propene 1-chloropropane 2-chloropropene

Columbia University C99ORG14.DOC S3443D Summer 99 Professor Grace B. Borowitz Exam No. 4 - Final July 1, 1999

CHE 321 Summer 2012 Exam 2 Form Select the correct number of chirality centers in heroin, the illicit drug shown below.

Chem 342 Organic Chemistry II Final Exam 13 May 2009

Transcription:

KWANTLEN UNIVERSITY LLEGE EMISTRY 2320 - R10 rganic hemistry I ecember 14, 2001 180 Total Marks Time: 3 hours (180 minutes) Budget your time and good luck!! NAME: This paper consists of 12 pages (11 questions) (including this title page). Ensure that you have a complete paper (data pages will be provided). Molecular models may be used during this examination. 1 2 Grading Scheme F The Exam Question 3 4 5 6 7 8 9 10 11 14 18 18 18 13 16 24 20 14 10 15 Mark Maximum Total Percent 180 %

Question 1. (14 Marks) ircle the crect answer f each of the following: a) F the following three constitutional isomers (all 49): (5) X Y Z Which would give the fastest reaction with I - in acetone (solvent)? X Y Z Which would require the lowest temperature f solvolysis (2)? X Y Z Which could produce the largest number of E2 products? X Y Z Which could be fmed from an alkene with /22? X Y Z Which could not be fmed from an alkane with 2/_? X Y Z Which could not be easily fmed from an alcohol with P3? X Y Z b) This question is based upon the three compounds (B, and F) shown below: B F Which compound would have the: (4) highest boiling point: B F highest vapour pressure: B F lowest water solubility: B F largest pka value: B F c) F the reaction below: (5) X Nu Solvent i) Which leaving group (X) would yield the fastest reaction? l I ii) Which would be the better nucleophile? 3-3 32 iii) Which nucleophile would give the greatest yield of SN2 product? Nu - - N - iv) Which nucleophile would give the greatest yield of E2 product? - - v) Which solvent would be better f solvolysis; i.e., no other Nu present? N -

Question 2. (18 Marks) The following optically pure compound was treated with 2 in the presence of UV radiation to produce a mixture of monobrominated compounds. Provide the crect number f each of the terms indicated. (4.5) pair(s) of enatiomers UV 2 optically pure compound(s) meso compound(s) The products were fmed as a result of a { concerted / non-concerted } process best described as { regioselective / stereoselective } in which the { intermediate / transition state } was most likely a { bromonium ion / free radical / carbocation }. (4) The following compound A was isolated from a similar bromination process. (4.5) omplete structure B so that it is the enantiomer of compound A. omplete structure so that it is a confmational isomer of compound A. omplete structure so that it is a diastereomer of compound A. A 3 B 3 In compound A, the carbon atom containing the atom is best labelled as: (1) R S In compound A, the carbon atom containing the atom is best labelled as: (1) R S omplete the structure of the maj product and the min product fmed in the E2 reaction of compound A with NaN2. (3) A 3 NaN 2 ether maj min

Question 3. (18 Marks) Provide/complete the structures to illustrate the following: a) keto-enol tautomerism b) a resonance stabilized cation c) an achiral dimethylcyclohexane which d) a gauche confmer of hexane (3 to 4) requires no stereochemical prefixes e) an unsaturated 612 isomer which f) a saturated 6102 isomer which contains only allylic atoms is a meso compound g) an isomer of 511 which could h) a stronger base than 32 - not undergo an E2 reaction with - N2 i) a chlobicyclo[2.2.1]heptan-2-one j) a methylbicyclo[4.2.1]nonene isomer that requires the prefix endo isomer that requires the prefix anti k) an unsaturated isomer of 46F2 l) the E,Z stereoisomer of 3,5-dichlo-2,4- which is non-polar pentadienal

Question 4. (18 Marks) a) omplete the structures of compounds B and, each fmed from the reaction of compound A excess 3Mg followed by an acidic wk-up. (3) A 1. 3 Mg 2. 3 B ompound A is a meso compound: (1) Yes No ompounds B and are: (1) diastereomers enantiomers confmers ompounds B and are each: (1) optically pure achiral racemic The reaction with 3Mg is best described as a(n): (1) electrophilic addition of 3 nucleophilic addition of 3 electrophilic addition of 3 - nucleophilic addition of 3 - b) omplete the structures of compounds E and F, each fmed from the reaction of the optically pure compound with dilute acid. Assume that no rearrangements occur. (3) 3 2 3 E F Which compound is optically pure? (1) E F The reaction is best described as the: (1) electrophilic addition of nucleophilic addition of c) omplete the structures of compounds and I, each fmed from the reaction of compound G with l2. NTE: The t-butyl group is much larger than a l atom. (3) 3 3 l 2 3 G l 4 I Which compound is me stable? (1) I This reaction is best described as a { regioselective / stereoselective } { syn / anti } addition. (2)

Question 5. (13 Marks) a) Using structural fmulas and reaction arrows, including the use of "electron arrows", clearly show the steps of a reasonable mechanism f the following transfmation. (5) concentrated 3 3 3 3 2 S 4 3 3 3 heat 3 b) lever alvin, that renowned EM 2320 graduate, set out to prepare benzyl t-butyl ether. e tried the following two methods; but unftunately, only one of them gave good yields of the desired product. Indicate which process would give the best yield (giving the structure of the benzyl t-butyl ether), and f the other one, give the structure of the maj product(s) which would have been isolated instead. (4) 2-2 - c) Propose a structure f the maj product fmed in each of the following reactions. (4) NaI (1 equivalent) 2 2 Na 2 S acetone 2 3 acetone 5 10 I 4 8 S

Question 6. (16 Marks) In many reactions where me than one product MIGT be fmed, it is quite often found that one compound may be fmed to a greater extent than others. F each of the following reactions, circle the compound that would be the maj product. I ( 3 ) 3 - ( 3 ) 3 warm 3 3 3 S N 1 conditions I - 3 3 3 2 F NaI 2 I 2 F 2 acetone 2 2 I 3 l NaN 2 3 3 ether 3 3 3 R 3-2 l 1 mole l l

Question 7. (24 Marks) Provide the structure of the maj product expected in each of the following reactions. Include any pertinent stereochemistry where imptant. P P 3 ether 2 uli 2 2 1. 3 2 NaN 2 1. Tsl 2. 3 2. 3 2 - I 3 1. s 4 ether 2. NaS 3 2 S 4 2 g 2 2 Lindlar catalyst KMn 4 acidic 1. 3 2. Zn/ 2 R 3 2 Pt high P high T 2 2

Question 8. (20 Marks) Each of the following reactions produces two maj products. omplete the structure of each product (clearly showing any pertinent stereochemistry) and indicate the relationship between the two compounds; i.e., enantiomers, diastereomers, positional isomers, tautomers, not isomers, etc.... Provide the name of the type of reactive intermediate involved in the process (if there isn't any, put none). 3 3 3 3 2 3 3 3 3 intermediate: relationship: 1. B 3 3 3 3 2. 2 2 / - intermediate: relationship: = 2 excess 2 Pt intermediate: relationship: 3 2 3 I S N 1 conditions 3 3 intermediate: relationship: 3 2 3 UV intermediate: relationship:

Question 9. (14 Marks) Sidney Smart is having a really bad day at AME hemicals. e has treated isobutyl benzene with l2 in the presence of UV radiation and then boiled a ption of the resulting mixture of monochlide products in a mixture of ethanol and water. After isolating several compounds, he arranged to have their 1 NMR spectra taken. As you can guess, he has fgotten everything he once knew about chemical shifts, splitting patterns etc... elp out po Sidney by assigning the ptions of the molecule responsible f the signals in the 1 NMR spectrum of isobutylbenzene (1014), and then complete the structures of the compounds A (1013l), B (1012), (1014) and (1218).

Question 10. (10 Marks) lever alvin needs your help again, this time with a synthetic problem. e has a rush der f the two alcohols A and B below (constitutional isomers of each other). Propose suitable sequences of reactions (including the necessary reagents/solvents etc..) to prepare each of the two alcohols. You may use any inganic reagents in addition to the iginal starting materials (which you can use as many times as you need to). Show the structure of the maj product fmed after each reaction. 3 A 3 and 3 as the only B 2 2 3 sources of carbon

Question 11. (15 Marks) The optically pure compound A (614) had a strong band in the IR around 3400 cm -1, and could be converted to the optically pure compound B (612) with P. ompound B had a strong band in the IR around 1700 cm -1. Treatment of compound B with 2/Pt at high temperature and high pressure refmed compound A as a mixture of two diastereomers. Treatment of optically pure compound A ( the mixture of diastereomers) with concentrated 2S4 lead to the fmation of the achiral diastereomers and (both 612) as maj products. Treatment of compound with dilute acid produced the same achiral compound E (614) which had a strong band in the IR around 3400 cm -1. ompound E gave no reaction with P. Propose complete structures f compounds A ---> E in the boxes below. Make certain that any pertinent stereochemistry is clearly shown. A B E