CHEM 345 Problem Set 07 Key

Similar documents
Chem 263 March 7, 2006

REALLY, REALLY STRONG BASES. DO NOT FORGET THIS!!!!!

p Bonds as Electrophiles

Chapter 9 Aldehydes and Ketones Excluded Sections:

Loudon Chapter 19 Review: Aldehydes and Ketones CHEM 3331, Jacquie Richardson, Fall Page 1

ORGANIC - BROWN 8E CH ALDEHYDES AND KETONES.

Additions to the Carbonyl Groups

Reversible Additions to carbonyls: Weak Nucleophiles Relative Reactivity of carbonyls: Hydration of Ketones and Aldehydes

THE CHEMISTRY OF THE CARBONYL GROUP

Chem 263 Nov 14, e.g.: Fill the reagents to finish the reactions (only inorganic reagents)

Dr. Mohamed El-Newehy

ORGANIC - CLUTCH CH ALDEHYDES AND KETONES: NUCLEOPHILIC ADDITION

Chapter 12: Carbonyl Compounds II

Chem 263 Notes March 2, 2006

Lecture 15. More Carbonyl Chemistry. Alcohols React with Aldehydes and Ketones in two steps first O R'OH, H + OR" 2R"OH R + H 2 O OR" 3/8/16

Physical Properties. Alcohols can be: CH CH 2 OH CH 2 CH 3 C OH CH 3. Secondary alcohol. Primary alcohol. Tertiary alcohol

Reactions at α-position

Lecture Notes Chem 51C S. King. Chapter 20 Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation & Reduction

Synthesis of Nitriles a. dehydration of 1 amides using POCl 3 : b. SN2 reaction of cyanide ion on halides:

Carboxylic Acids and Nitriles

Section Practice Exam II Solutions

Chem 263 Nov 3, 2016

DAMIETTA UNIVERSITY CHEM-103: BASIC ORGANIC CHEMISTRY LECTURE

Suggested solutions for Chapter 6

Nucleophilic Addition Reactions of Carboxylic Acid Derivatives

Chapter 20 Carboxylic Acid Derivatives. Nucleophilic Acyl Substitution

Topic 9. Aldehydes & Ketones

2.222 Practice Problems 2003

But in organic terms: Oxidation: loss of H 2 ; addition of O or O 2 ; addition of X 2 (halogens).

MCAT Organic Chemistry Problem Drill 10: Aldehydes and Ketones

1- Reaction at the carbonyl carbon (Nucleophilic addition reactions).

The Claisen Condensation

Chemistry 14D Winter 2017 Final Exam Part A Page 1

18.8 Oxidation. Oxidation by silver ion requires an alkaline medium

Chapter 22 Amines. Nomenclature Amines are classified according to the degree of substitution at nitrogen.

When we deprotonate we generate enolates or enols. Mechanism for deprotonation: Resonance form of the anion:

Chapter 20 Carboxylic Acid Derivatives Nucleophilic Acyl Substitution

FIRST EXAMINATION. Name: CHM 332

Chapter 19 Substitutions at the Carbonyl Group

Chem 263 March 28, 2006

Lecture 3: Aldehydes and ketones

Chem 112A: Final Exam

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

Chapter 16 Aldehydes and Ketones I Nucleophilic Addition to the Carbonyl Group

b.p.=100 C b.p.=65 C b.p.=-25 C µ=1.69 D µ=2.0 D µ=1.3 D

c. Oxidizing agent shown here oxidizes 2º alcohols to ketones and 1º alcohols to carboxylic acids. 3º alcohols DO NOT REACT.

Chapter 20: Carboxylic Acids and Nitriles شیمی آلی 2

Enols and Enolates. A type of reaction with carbonyl compounds is an α-substitution (an electrophile adds to the α carbon of a carbonyl)

Aldehydes and Ketones

Aldehydes and Ketones : Aldol Reactions

Chapter 16 Aldehydes and Ketones I. Nucleophilic Addition to the Carbonyl Group

21.1 Introduction Carboxylic Acids Nomenclature of Carboxylic Acids. Acids Structure and Properties of Carboxylic Acids.

CHM 292 Final Exam Answer Key

CARBONYL COMPOUNDS: OXIDATION-REDUCTION REACTION

8-3 This exercise is worked out on page 293 as "Working with Concepts".

Ch 20 Carboxylic Acids and Nitriles

18.10 Conjugate Additions O O. O X BrCH 2 CH 2 CH 2 CCH 3 ± ± BrCH 2 CH 2 CH 2 CH 3. TsOH 1 O C O O W 3 CH 3 CCH 3 CH 3 CCH 2 CH 2 CH 2 CH 3

Chapter 11, Part 1: Polar substitution reactions involving alkyl halides

Chem 263 Nov 24, Properties of Carboxylic Acids

Chapter 20: Aldehydes and Ketones

Effect of nucleophile on reaction

REACTION AND SYNTHESIS REVIEW

Chemistry Final Examinations Summer 2006 answers

Aldehydes and Ketones Reactions. Dr. Sapna Gupta

75. A This is a Markovnikov addition reaction. In these reactions, the pielectrons in the alkene act as a nucleophile. The strongest electrophile will

Chapter 12 Alcohols from Carbonyl Compounds: Oxidation-Reduction and Organometallic Compounds

Homework for Chapter 7 Chem 2310

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

DAMIETTA UNIVERSITY. Energy Diagram of One-Step Exothermic Reaction

CHAPTER 23 HW: ENOLS + ENOLATES

CHAPTER 7. Further Reactions of Haloalkanes: Unimolecular Substitution and Pathways of Elimination

Module9. Nuclear Magnetic Resonance Spectroscopy Nuclear Magnetic Resonance (NMR) spectroscopy - Chemical shift - Integration of signal area

Ethers can be symmetrical or not:

Chapter 20: Aldehydes and Ketones

The problem is that your product still has a-protons, and can keep on forming enolates to get more methyl groups added:

Chapter 16. Aldehydes and Ketones I. Nucleophilic Addition to the Carbonyl Group. Physical Properties of Aldehydes and Ketones. Synthesis of Aldehydes

Chapter 19. Carbonyl Compounds III Reaction at the α-carbon

Chem 263 Nov 7, elimination reaction. There are many reagents that can be used for this reaction. Only three are given in this course:

Chapter 18: Ketones and Aldehydes. I. Introduction

TOK: The relationship between a reaction mechanism and the experimental evidence to support it could be discussed. See

CHEM 347 Organic Chemistry II (for Majors) Instructor: Paul J. Bracher. Quiz # 4. Due in Monsanto Hall 103 by: Friday, April 4 th, 2014, 7:00 p.m.

Aldol Reactions pka of a-h ~ 20

1/4/2011. Chapter 18 Aldehydes and Ketones Reaction at the -carbon of carbonyl compounds

Chapter 19 Carboxylic Acids

Chapter 9:Nucleophiles & Substitution Reactions

Chapter 22 Enols and Enolates

Chapter 20: Aldehydes and Ketones

CHEM 343 Principles of Organic Chemistry II Summer Instructor: Paul J. Bracher. Quiz # 3. Monday, July 21 st, :30 a.m.

Carbonyl Chemistry IV + C O C. Lecture 10. Chemistry /30/02

22.7 Reactions of Amines: A Review and a Preview

Aldehydes and Ketones 2. Based on Organic Chemistry, J. G. Smith 3rde.

Aldehydes, Ketones and Carboxylic acids

Chem 345 Reaction List: Chem 343 Reactions: Page 1 (You do not need to know the mechanism for the reactions in the boxes).

Lecture 18. Oxidation and Reduction. Oxidation. Reduction O CH 4 CH 3 OH H C H. Chemistry 328N

Important Note: We will NOT accept papers written in pencil back for re-marking after they have been returned to you. Please do not ask!

12. Aldehydes & Ketones (text )

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

Loudon Chapter 10 Review: Alcohols & Thiols Jacquie Richardson, CU Boulder Last updated 4/26/2016

Reactions SN2 and SN1

Nuggets of Knowledge for Chapter 17 Dienes and Aromaticity Chem 2320

Transcription:

CHEM 345 Problem Set 07 Key 1.) Fill in the appropriate reaction arrow. The starting material is on the left, the product is on the right. Use. Simple Ring Size. 5 and 6 are favored. 3 is not. That s it. or a. b. c. pka Table R=H or sp 3 C -5 0 5 10 15 20 25 35 45 HCl H R H R H R R H R H R R H R H H R R H R R H H R SH HC

2.) This is a critical thinking problem. Using the base strengths of the anions, predict which reaction arrow you should use. The pka table on the previous page is one you should know. will have it on the first exam. After that Assume all of these products have approximately the same basicity (conj. pka ~15). ( ) Point the large arrow to the weakest base. f the numbers are close (say within six or so, it is reversible. f it is ten, then it can be reversible but does slow slowly. f it is greater than ten, not gonna happen) a. conj. pka ~ 15 H Me conj. pka ~ 15 b. Cl H conj. pka ~ -5 Me Cl conj. pka ~ 15 c. H conj. pka ~ 20 Me conj. pka ~ 15 d. H conj. pka ~ 45 Me conj. pka ~ 15 e. conj. pka ~ 10 C H Me C conj. pka ~ 15

3.) Draw mechanisms for the following reactions. Label the products as acetals, hemiacetals, imines, or cyanohydrins. A. cat. ah H H 2 H Hemiacetal B. H cat. H 2 S 4 H 2 H Hemiacetal

C. H cat. H 2 S 4 EtH Acetal

D. cat. AcH H 2 imine

E. cat. ah HC H Cyanohydrin C F. KC AcH H Cyanohydrin C

4.) Predict the products: A. cat. H 2 S 4 H B. KC H H C C. H 2 cat. AcH D. cat. H 2 S 4 H optically active H optically active E. cat. AcH H 2 F. cat. ah C HC H

5.) The following compounds come from a carbonyl (ketone or aldehyde). Fill in the boxes A. H cat. H 2 S 4 H ketone or aldehyde conditions B. cat. H 2 S 4 Ph H 2 Ph ketone or aldehyde conditions C. cat. H 2 S 4 H ketone or aldehyde conditions D. H cat. ah, HC or KC, AcH optically active C optically active ketone or aldehyde conditions E. ketone or aldehyde H cat. H 2 S 4 conditions H

6.) Draw the mechanisms for the following reactions. Show all curved arrows and intermediates: a. H 2 trace AcH s the product? Why or why not? Two Possibilities: The product is achiral, so it is neither optically active nor. r

6.) continued: b. Me Me H 2 trace AcH

7.) Predict the products: a.) H 2 Ph Ph trace AcH Major b.) H 2 trace AcH H 2 3 signals in 1 H MR

8.) Critical thinking: The following acetals when exposed to acid and water, aldehydes are formed. Which acetal is cleaved faster and why? Draw the mechanism of the formation of benzaldehyde from each of these acetals. Acetal A Acetal B

8.) Continued Acetal B is cleaved slower than A. When the first is protonated and leaves to form the carbocation, the is still tethered and will back before water can add. n the case of acetal A, the becomes completely detached and becomes less likely to come back as it diffuses away.

9.) Write the mechanisms for the following problems: a. abd 4 EtH H D b. H 1.) excess MeMgBr/Et 2 2.) H 3 + H H

a.) 10.) Using CD 3 D and abd 4 as your sole sources of deuterium, synthesize the following compounds. D abd 4 EtH H b.) D D 1.) Et 2 2.) H 3 + MgBr H D D PCC CH 2 Cl 2 c.) D D H 1.) Et 2 2.) H 3 + D D MgBr CD 3 D H H D D HBr Mg Et 2 D D H Br 1.) Et 2 2.) H 3 + MgBr PCC CH 2 Cl 2 CD 3 D d.) D D CD 3 Br acd 3 ah CD 3 D

e.) H 1.) Et 2 Mg 2.) H 3 + Et 2 MgBr Br CD 3 H H CD 3 CD 3 PBr 3 D 3 C Br Mg Et 2 D 3 C MgBr 1.) Et 2 2.) H 3 + H PBr 3 CD 3 f.) CD 3 D CD 3 1.) Et 2 2.) H 3 + Mg Et 2 H BrMg CD 3 Br CD 3 g.) CD 3 D PBr 3 D 3 C Br Mg Et 2 CD 3 D D 3 C MgBr 1.) Et 2 2.) H 3 + PBr 3 H CD 3 h.) D CD 3 D a D h. is just an acid base reaction. That is all. MgBr

11.) MR Problem: Predict the MRs of the following compounds:

12.) C 9 H 8. The MR is from the Sigma Aldrich Company.

13.) Chem 343 review: S 1 vs. S 2 vs. E2 The nucleophiles below (except for one) are all good enough nucleophiles to work in a S 2 reaction (except one). They have various base strengths which is inversely proportional to the strength of the conjugate acid. The basicity of a nucleophile as well as the hindrance of the electrophile provides a good measure whether a reaction will undergo S 1 or S 2 or E2. f the alpha carbon (the carbon connected to the good leaving group) is tertiary, then only nucleophiles whose conjugate acids have a pka less than 5 will give S 1 products in an appreciative amount. f the pka is above 5, then E2 becomes the major pathway. (At pka of five expect a complex mixture of E2 and S 1 products). f the alpha carbon is secondary, when the conjugate acid is 10 or below, then S 2 is the major product. When it is 15 or above, then E2 is the major product. f the alpha carbon is primary, the major pathway is S 2 except when a bulky base like tbu - is used, then E2 happens. f the alpha carbon is a methyl group, then E2 is impossible and S 2 is the only option besides no reaction. Even tbu - will react with Me in a S 2 reaction. Write next to each nucleophile what the approximate pka of its conjugate acid is. Then, react it with each of the four electrophiles. Write the major pathway and major product. (32 reactions total). ucleophiles Electrophiles conj. pka ~ 25 Br conj. pka ~ -5 C conj. pka ~ 15 conj. pka ~ 15 optically active S conj. pka ~ 10 conj. pka ~ 10 C conj. pka ~ 5 conj. pka ~ 10 Me

a. Br S 1 Br b. Br S 2 Br optically active optically active c. Br S 2 Br d. e. Br Me S 2 E2 MeBr f. E2 optically active g. E2 h. Me S 2

i. E2 j. S 2 Ph optically active optically active k. S 2 l. Me S 2 Me m. C E2 n. C E2 optically active o. C S 2 p. C S 2 Me

r. E2 s. E2 optically active t. S 2 u. S 2 v. S Me E2 w. S 2 S S optically active optically active x. S S 2 S y. S Me S 2 S

z. C E2 aa. C S 2 C optically active optically active ab. C S 2 C ac. ad. C Me S 2 E2 and S 1 Me C ae. S 2 optically active af. S 2 optically active ag. S 2 Me

14.) From the MR provided, determine the structure of the following compound. Assign the peaks Ha, Hb, Hc etc. accordingly. The MR spectra are from the Sigma-Aldrich Corporation. ntegrations are in bold above each signal. C 8 H 6 3 6 DBE

15.) From the MR provided, determine the structure of the following compound. Assign the peaks Ha, Hb, Hc etc. accordingly. The MR spectra are from the Sigma-Aldrich Corporation. ntegrations are in bold above each signal. C 4 H 9 1 DBE

16.) From the MR provided, determine the structure of the following compound. Assign the peaks Ha, Hb, Hc etc. accordingly. The MR spectra are from the Sigma-Aldrich Corporation. ntegrations are in bold above each signal. All signals are shown. C 3 H 6 3 1 DBE

17.) From the MR provided, determine the structure of the following compound. Assign the peaks Ha, Hb, Hc etc. accordingly. The MR spectra are from the Sigma-Aldrich Corporation. ntegrations are in bold above each signal. C 9 H 12 3 4 DBE

18.) From the MR provided, determine the structure of the following compound. The MR spectra are from the Sigma-Aldrich Corporation. ntegrations are in bold above each signal. C 9 H 10 5 DBE

19.) Sometimes it is possible to combine two reactions in the same pot to get a new reaction. Draw the mechanism for the following reactions a.) AcH H H 3 b.) AcH KC H C

c.) H 4 Cl H 2 KC C

20.) ne way to make amines is to treat an imine with sodium borohydride in EtH. Draw the mechanism of the following two step sequence. AcH MeH 2 abh 4 EtH H

21.) Sodium cyanoborohydride is a weaker hydride source than sodium borohydride. Why is sodium cyanoborohydride weaker than sodium borohydride? The nitrile group is a strongly electronegative and electron withdrawing group. t pulls electron density from the boron which then pulls electron density from the hydrogens. The hydrogens then have less electron density and are thus less likely to attack a carbonyl. H H B a C Sodium Cyanoborohydride H t is a very handy reagent, because you do not need to preform the imine. The imine can be made in situ, so a two step procedure becomes a one step procedure. Draw the mechanism for the reaction. Hint: This goes through an imine reaction. n this mechanism try to avoid making a negative nitrogen. egative nitrogens are very basic and you should try to avoid them if possible. AcH MeH 2 abh 3 C H What goes wrong if abh4 is used instead? What major side reaction takes place? The aldehyde can be reduced by sodium borohydride to give an alcohol.

Chem 345 Reaction Sheets: Acetal formation cat. H 2 S 4 H Mechanism: cat. H 2 S 4 H Summary (Key words): Acetals are made under acidic conditions, so no basic compounds can be used in the mechanism. The mechanism consists of hemiacetal formation followed by an S1 reaction. The carbonyl oxygen is lost as water. Acetals are useful to protect ketones and aldehydes from nucleophiles such as Grignards. Acetal formation is reversible.

Chem 345 Reaction Sheets: Acetal Cleavage cat. H 2 S 4 H 2 H H Mechanism: cat. H 2 S 4 H 2 Summary (Key words): Acetals are cleaved by acid and water. The carbonyl oxygen comes from water. Acetals are useful to protect ketones and aldehydes from nucleophiles such as Grignards. All steps in the mechanism are reversible.

Chem 345 Reaction Sheets: mine Formation cat. H 2 S 4 H 2 Mechanism: cat. H 2 S 4 H 2 Summary (Key words): f a strong acid is used, then it must be catalytic. t is not necessary for the carbonyl before the amine attacks. Reaction generates water. All steps are reversible.

Chem 345 Reaction Sheets: mine Hydrolysis cat. H 2 S 4 H 2 H 2 Mechanism: cat. H 2 S 4 H 2 Summary (Key words): mines are slightly basic. t is not necessary for there to be an acid catalyst. mines are water sensitive and are readily converted to carbonyls. All steps are reversible.

Chem 345 Reaction Sheets: Cyanohydrin Formation AcH, KC or cat. ah, HC C H Mechanisms: AcH, KC cat. ah, HC Summary (Key words): Reaction is reversible. Cyanohydrins are base sensitive. Cyanide is a good nucleophile. t attacks the carbonyl directly.

Chem 345 Reaction Sheets: Cyanohydrin cleavage H cat. ah C Mechanism: H cat. ah C Summary (Key words): All steps reversible. Cyanohydrins are base sensitive.

Chem 345 Reaction Sheets: Reduction of a ketone with sodium borohydride abh 4 EtH H Mechanism: abh 4 EtH Summary (Key words): Addition of the hydride to carbonyl is irreversible. The hydrogen that attacks the carbonyl carbon comes from sodium borohydride. The proton that adds to the oxygen comes from the alcohol solvent. Sodium borohydride is basic. t can also deprotonate H s (cyanohydrins, hemiacetals)

Chem 345 Reaction Sheets: Reaction of a ketone with a Grignard Reagent 1.) MeMgBr, Et 2 2.) H 3 + H Mechanism: 1.) MeMgBr, Et 2 2.) H 3 + Preparation of a Grignard Reagent: Mg MeBr MeMgBr Summary (Key words): Addition of the carbon group to the carbonyl is irreversible. Always a two step procedure. Grignards are really strong bases. t will react with acidic hydrogens very quickly. This includes H s on cyanohydrins or hemiacetals.