CONJUGATED PI SYSTEMS AND PERICYCLIC REACTIONS

Similar documents
Chapter 13 Conjugated Unsaturated Systems

Chapter 13. Conjugated Unsaturated Systems. +,., - Allyl. What is a conjugated system? AllylicChlorination (High Temperature)

Chapter 14: Conjugated Dienes

and Ultraviolet Spectroscopy

Conjugated Dienes and Ultraviolet Spectroscopy

Homework for Chapter 17 Chem 2320

Chapter 15: Conjugated Systems, Orbital Symmetry, and UV Spectroscopy

Ethers. Chapter 14: Ethers, Epoxides, & Sulfides. General Formula: Types: a) Symmetrical: Examples: b) Unsymmetrical: Examples: Physical Properties:

Chapter 14: Dienes and Conjugation. Topics Dienes: Naming and Properties. Conjugation. 1,2 vs 1,4 addition and the stability of the allyl cation

Conjugated Systems. With conjugated double bonds resonance structures can be drawn

There are several possible arrangements for a molecule which contains two double bonds (diene): 1. Isolated: (two or more single bonds between them)

Lecture Notes Chem 51B S. King I. Conjugation

17.1 Classes of Dienes

Nuggets of Knowledge for Chapter 17 Dienes and Aromaticity Chem 2320

Learning Guide for Chapter 17 - Dienes

Conjugated Systems, Orbital Symmetry and UV Spectroscopy

17.1 Classes of Dienes

Dienes & Polyenes: An overview and two key reactions (Ch )

Conjugated Dienes. Chapter 14 Organic Chemistry, 8 th Edition John E. McMurry

Conjugated Dienes. Chapter 14 Organic Chemistry, 8 th Edition John E. McMurry

Chapter 14: Conjugated Dienes and Ultraviolet Spectroscopy Diene: molecule with two double bonds Conjugated diene: alternating double and single bonds

Organic Chemistry II / CHEM 252 Chapter 13 Conjugated Unsaturated Systems

Chapter 15 Dienes, Resonance, and Aromaticity

Exam. Name. MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

Ch 14 Conjugated Dienes and UV Spectroscopy

CARBOXYLIC ACIDS AND THEIR DERIVATIVES. 3. Predict the relative acidity and basicity of compounds and ions. Important criteria include:

CHAPTER 9 THEORY OF RESONANCE BY, G.DEEPA

CHEMISTRY Topic #3: Addition Reactions of Conjugated Dienes Spring 2017 Dr. Susan Findlay

Lecture 22 Organic Chemistry 1

Cyclooctatetraene (2R)-2-phenylbutane benzyl chloride cycloocta-1,3,5,7-tetraene

COURSE OBJECTIVES / OUTCOMES / COMPETENCIES.

11/5/ Conjugated Dienes. Conjugated Dienes. Conjugated Dienes. Heats of Hydrogenation

CHEM 330. Topics Discussed on Nov. 25

THE DIELS-ALDER REACTION

3 - CONJUGATION. More than one double bond can be in a given compound: n=0

CHEMISTRY MIDTERM # 2 ANSWER KEY July 10, 2002

3 - CONJUGATION. More than one double bond can be in a given compound: n=0

Department of Chemistry SUNY/Oneonta. Chem Organic Chemistry I. Examination #4 - December 9, 2002 ANSWERS

Diels-Alder Cycloaddition

Review and Preview. Coursepack: pp (14.6 is FYI only)

CARBOXYLIC ACIDS AND THEIR DERIVATIVES

Pericyclic reactions

Departmental Final Examination. Organic Chemistry I Caffein

ORGANIC - BRUICE 8E CH.8 - DELOCALIZED ELECTRONS AND THEIR EFFECT

10.12 The Diels-Alder Reaction. Synthetic method for preparing compounds containing a cyclohexene ring

3) The delocalized π system in benzene is formed by a cyclic overlap of 6 orbitals. A) s B) p C) sp D) sp2 E) sp3

Christopher M. Hadad Chemistry 253N Spring Final Exam. Name (PRINT) ANSWER KEY I have neither given nor received aid on this exam (SIGN)

ADDITION OF HYDROGEN HALIDES TO CONJUGATED DIENES A. 1,2- and 1,4-Additions 700 CHAPTER 15 DIENES, RESONANCE, AND AROMATICITY

1. Which of the following reactions would have the smallest energy of activation?.

Chapter 13 Conjugated Unsaturated Systems

a) Write the mechanism of Friedel-Crafts alkylation of ethyl benzene to give 1,4- diethylbenzene. Show all arrow pushing.

UNIVERSITY OF CALGARY FACULTY OF SCIENCE MIDTERM EXAMINATION CHEMISTRY 353 READ ALL THE INSTRUCTIONS CAREFULLY

Organic Chemistry: CHEM2322

MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question. A) I B) II C) III D) IV E) V

NUCLEAR MAGNETIC RESONANCE AND INTRODUCTION TO MASS SPECTROMETRY

Loudon Chapter 15 Review: Dienes and Aromaticity Jacquie Richardson, CU Boulder Last updated 1/28/2019

ORGANIC - BROWN 8E CH DIENES, CONJUGATED SYSTEMS, AND PERICYCLIC REACTIONS

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

1) What is the major product of the following reaction? HBr. HBr+BrBr

Organic Chemistry I (Chem340), Spring Final Exam

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

Organic Chemistry CHM 224

Chemistry 2541, Fall 2017 Midterm Exam 2 (100 points)

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

Chem 263 Notes Sept. 26, 2013

Dr. Dina akhotmah-232 1

Terms used in UV / Visible Spectroscopy

CHEMISTRY 112A FALL 2015 FINAL EXAM DECEMBER 16, 2015 NAME- WRITE BIG STUDENT ID: SECTION AND/OR GSI IF YOU ARE IN THE LABORATORY COURSE:

nsaturated Hydrocarbons: Alkenes, Cycloalkenes and Dienes

trans-cyclooctene 4-fluoro-1-butanol 2-cyclohexenol 4. (5 pts) Provide structural formula for each of the following molecules: Br OH Cl OH

Advanced Organic Chemistry

Name: CHEM 633/634 Problem Set 1: Review Due Tues, Aug 29, 2017 (First Lecture!)

More Tutorial at

Pericyclic Reactions

Chapter 6: Organic Halogen Compounds; Substitution and Elimination Reactions

Name: Student Number: University of Manitoba - Department of Chemistry CHEM Introductory Organic Chemistry II - Term Test 1

25.3 THE CHEMISTRY OF FURAN, PYRROLE, AND THIOPHENE

Chapter 27 Pericyclic Reactions

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

Chapter 15 Conjugated Systems

Chem 263 Sept 22, Beta-carotene (depicted below) is the orange-red colour in carrots. β-carotene

CHAPTER 3 ALKENES, ALKYNES & CONJUGATE DIENES

REACTIONS OF AROMATIC COMPOUNDS

Only five of the molecules below may be prepared as the sole product of allylic halogenation of the respective alkene. Circle those five.

Model 1 Homolysis Reactions are Highly Endothermic

Hour Examination # 1

Chemistry 234 Exam 1 (Gray) The Periodic Table

Learning Guide for Chapter 11 - Alkenes I

AMINES. 3. From your knowledge of the effects involved, predict or explain experimental results. Important areas include:

Part I. Multiple choice. (4 points each.) Choose the one best answer and mark your answer on the ScanTron sheet.

ORGANIC - BROWN 8E CH.8 - HALOALKANES, HALOGENATION AND RADICALS

EASTERN ARIZONA COLLEGE General Organic Chemistry I

235 Organic II. Final Exam Review REACTIONS OF CONJUGATED DIENES 1,2 VS 1,4 ADDITION REACTIONS OF CONJUGATED DIENES

AMINES. 4. From your knowledge of the effects involved, predict or explain experimental results. Important areas include:

use iso-, tert-, sec- prefixes in your substituent names, where necessary

C h a p t e r E i g h t: Alkenes: Structure and Preparation via Elimination Reactions. 5-Androstene, the parent alkene for most anabolic steroids

NBS, CCl 4 heat A B C D

The C-X bond gets longerand weakergoing down the periodic table.

Preparation of Alkyl Halides, R-X. Reaction of alkanes with Cl 2 & Br 2 (F 2 is too reactive, I 2 is unreactive): R + X X 2.

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

Transcription:

CNJUGATED PI SYSTEMS AND PERICYCLIC REACTINS A STUDENT SULD BE ABLE T: 1. Recognize and give examples of conjugated, isolated, and cumulated dienes, and of allylic intermediates. Also, name given the structure, and draw the structure given the name, of polyenes (review). Distinguish conjgated dienes as s-cis or s-trans. 2. Distinguish resonance structures from other types, draw resonance structures of given species, and predict the relative stabilities of such structures (review). 3. Predict both the orders of diene and carbocation stabilities, and the relative reactivities of compounds in reactions proceeding by way of these intermediates. Diene stabilities: conjugated > isolated > cumulated Carbocations: allylic > 3 > allyl > 2 > 1 > C 3 > vinylic 4. Propose mechanisms for reactions involving conjugated systems, and explain and predict experimental results in such reactions from knowledge of the mechanisms involved. Important reactions are: Additions to conjugated dienes involving carbocations (Markovnikov) and free radicals (anti-markovnikov addition of Br). Factors contributing to the 1,2- vs. 1,4- addition conflict are important. The Diels-Alder reaction. Endo product is favored over exo. The starting diene must be conjugated and in the s-cis conformation. These reactions are faster when: 1) The diene has electron-releasing (usually alkyl) groups attached to it, and the dienophile has electron-withdrawing groups attached to it, and 2) vice versa. ther pericyclic reactions 5. Given the starting material and reaction conditions, predict the product(s) of reactions involving allylic intermediates and diene starting materials. Important reactions include: Free radical substitution at allylic positions (review) Addition reactions to dienes (1,2 and 1,4 additions) The Diels-Alder reaction, and other pericyclic reactions 6. Devise syntheses of, or syntheses employing, dienes. 7. Identify and explain the processes involved in UV-Visible spectroscopy, including: The importance of the ighest ccupied and Lowest Unoccupied Molecular rbitals The energy, frequency, and wavelength relationships between ultraviolet, visible, and other radiation. Alkenes and nonconjugated dienes have absoption maxima at wavelengths less than 200 nm, while conjugated systems have maxima at wavelengths greater than 200 nm. More conjugation gives absorption maxima at longer wavelengths.

To best prepare for this module, please work Chapter 17 Skill Builder problems in the textbook. A STUDENT W AS MASTERED TE BJECTIVES N TE PREVIUS PAGE SULD BE ABLE T SLVE TE FLLWING PRBLEMS AND RELATED NES: 1.1 Draw an example of each of the following. a) an allylic carbocation b) a cumulated diene 1.2 Name each of the following. a) C 3 b) C 3 c) \ / \ / C=C C 3 C=C C 2 C 3 / \ / / \ / C=C C=C / \ / \ C 3 1.3 Draw each of the following. a) 1,3-cyclohexadiene b) allyl chloride c) trans-1,3-pentadiene Is this s-cis or s-trans? 2.1 Draw resonance structures of the species indicated. a) b) C2 total: five forms 2.2 Which of the structures shown contributes more to the resonance hybrid? C 3 C 3 A. C 3 -C-C=C 2 B. C 3 -C=C-C 2

2.3 Which of these is a valid resonance structure of? A B C. D 3.1 a) Which of the following dienes is the most stable? b) Which is the least stable? c)which one has an absorption maximum above 200 nm in its UV-Vis spectrum? A. C=C2 B. C=C2 C. C=C2 D. =C=C2 3.2 a) Which of the following carbocations is the most stable? b) Which is the least stable? A. C 2 CC=C 2 B. C 3 C=CC 2 C. 2 C=CC 2 C 2 D. C 3 C=CC 3 C 3 C 3 C 3 C 3 3.3 a) Which of the following free radicals is the most stable? b) Which is the least stable? A. C2 B. C3 C. C3 D. C3 4.1 Propose a mechanism for each of the following reactions. light a) 2 C=C-CD 3 Cl 2 -------> DCl 2 C=C-CD 2 Cl D 2 C=C-C 2 Cl 3 b) 2 C=C-C=C 2 2 -------> 3 C-C=C-C 2 4.2 Arrange these dienes based on their reactivity as a Diels-Alder diene in a reaction with maleic anhydride, fastest first. a) =C2 b) C3 c) C3 d) C3 4.3 Arrange these dienophiles based on their reactivity as Diels-Alder dieneophiles reacting with cyclopentadiene, fastest first. a) 2C=C2 b) c) d) = =

4.4 Draw mechanistic arrows for these pericyclic reactions. a) b) c) d) 5. Predict the product or products of each of the following reactions. Indicate stereoisomers where they are produced. high temperature a) Br2 ----------------------> b) CCl4, dark Br2 ----------------> c) 2 C=C-C=C 2 I(one mole) Which is major at low temperature? high temp? d) C 2=C-C=C 2 ------> e) 2C=C-C N --- f) ------> g)

6. Propose a synthesis of each of the compounds shown, from the given starting material and any other needed reagent. a) from b) from c) C3 from C3C CC 3 C3 d) C2 from 7. a) Circle the chromophore in each of these molecules. b) Which has the largest difference in energy between the M and LUM? c) Which has the largest max in the UV/Vis range?

SLUTINS T SAMPLE PRBLEMS: 1.1 a) an allylic carbocation b) a cumulated diene C 3 C=C-C 2 2 C=C=C 2 (There are many other possible examples here.) 1.2 a) 2,4-dimethyl-1,3-pentadiene b) trans,cis-2,4-heptadiene or (2E,4Z)-2,4-heptadiene c) 1,3,5,7-cyclooctatetraene 1.3 a) 1,3-cyclohexadiene (s-cis) b) allyl chloride c) trans-1,3-pentadiene C 3 \ / 2C=CC 2Cl C=C / \ 2C=C 2.1 Resonance structures: a) b) C2 C2 C2 C2 C2 2.2 A: 3 o allylic carbocation > 1 o allylic. Carbocation stability is more important to factor in, vs alkene stability. 2.3 C 3.1 a) Most stable C; b) least stable D; c) absorption maximum above 200 nm, C. 3.2 a) Most stable B (allylic); b) least stable D (vinylic) 3.3 a) Most stable B (allylic and 3 o ) ; b) least stable C (vinylic) 4.1 light a) 2 C=C-CD 3 Cl 2 -------> DCl 2 C=C-CD 2 Cl D 2 C=C-C 2 Cl light Initiation: Cl 2 ------> 2 Cl Propagation: Cl 2 C=CCD 3 ---> DCl 2 C=C-CD 2 <---> C 2 -C=CD 2 then 2 C=C-CD 2 Cl 2 ---> Cl 2 C=C-CD 2 Cl or C 2 -C=CD 2 Cl 2 ---> Cl ClC 2 -C=CD 2 (The termination steps have been omitted).

3 4.1 b) 2 C=C-C=C 2 2 -------> 3 C-C=C-C 2 4.2 C 4.3 D 2 C=C-C=C 2 3 ---> 2 3 C-C C=C 2 <---> 3 C-C=C-C 2 3 C-C=C-C 2 2 ---> 3 C-C=C-C 2 2 3 C-C=C-C 2 2 2 ---> 3 3 C-C=C-C 2 (Note: C 3 CC=C 2 also forms) 4.4 arrows can go clockwise or counterclockwise, as long as they re all in the same direction. a) b) c) d) 5. The product or products: a) high temperature Br2 ----------------------> Br enantiomer Br b) CCl4, dark Br2 ----------------> Br Br and its enantiomer peroxides c) 2 C=C-C=C 2 I (one mole) 2 C=C-CI-C 3 (R and S) C 3 -C=C-C 2 I (cis and trans) At low temp, 2 C=C-CI-C 3 is major; 1,2 product forms fastest At high temp, C 3 C=C-C 2 I is major; this 1,4 product is more stable

d) C2=C-C=C 2 ------> e) 2C=C-C N ----> same as CN endo CN f) -----> same as g) 6. Synthesis problems: a) Br 2 -------> 2 KtBu, heat -----------------> Br Br Also K: 1. NBS, RR (or Br 2 with heat or light), then KtBu b) C2=C-C=C2 ----> c) C3C CC 3 ----> C3 C3 d) 2C=CC2 ----> C2 same as C2

7. a) b) A: largest energy gap for least conjugation c) C: max is inversely related to energy

Name Third Drill Test, (Sample A) rganic Chemistry 2220DR Answer All Questions 1) Name: C 3C2 \ / 2) Draw 2-isopropyl-1,3-cycloheptadiene C=C / \ C 3 / Br C=C / \ C 2 C 3 3) a) Which of the compounds shown is the MST stable? b) Which one has an absorption maximum > 200 nm in its UV-visible spectrum? A. C C2 B. C=C2 C. CC3 D. C=C2 4) Predict the product or products (if any) of each of the following reactions. a) -C-C=C 2 3 b) C 2=C C=C 2 2 ---------> c) C2 Cl2 light 5) Propose a Diels-Alder synthesis of the compound shown. 6) Draw a resonance structure for:.. C2 7) Which of the following dienes gives the SLWEST Diels-Alder reaction? C2 C3 C2 C2 C3 C3 C3 C3 8) Propose a mechanism for: C 3 C=C-C=C 2 Cl C 3 C 2 -C=C-C 2 Cl

Name Third Drill Test (Sample B) rganic Chemistry 2220DR Answer All Questions 1. a) Give the complete IUPAC name of each compound. b) Classify each of the dienes as conjugated, cumulated, or isolated. c) Which of these absorbs UV-visible light at a longer wavelength? A. B. 2. Draw the structure(s) of the organic product(s) of each of the following reactions. a) Cl 2 --------> light b) -------> c) C 3 C 3 =C C= -----> 3. Propose a synthesis of each of the compounds shown from the indicated starting materials and any other needed reagents. a) C from

b) C 3 C=CC 2 Br from C 3 C 2 CC 3 4. Which of the following cations is the most stable? Which is least stable? A. B. C. 5. Propose a mechanism for the following reaction. 2 ------> 6. Draw a resonance structure of the one shown. C 3 C 2 C=C C=C C 2 C 3 C 2