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

Similar documents
CHEM 345 Problem Set 07 Key

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

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

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

CARBONYL COMPOUNDS: OXIDATION-REDUCTION REACTION

12.5 Organometallic Compounds

DAMIETTA UNIVERSITY. Energy Diagram of One-Step Exothermic Reaction

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

Organometallic Reagents

Chapter 9 Aldehydes and Ketones Excluded Sections:

ORGANIC - BROWN 8E CH ALDEHYDES AND KETONES.

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

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

Reducing Agents. Linda M. Sweeting 1998

Topic 6 Alkyl halide and carbonyl compounds Organic compounds containing a halogen

Topic 6 Alkyl halide and carbonyl compounds Organic compounds containing a halogen

ALCOHOLS AND PHENOLS

Lecture 3: Aldehydes and ketones

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

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

Chem 263 Notes March 2, 2006

Alcohols. Have seen many reactions to synthesize alcohols: In this chapter we will study reactions of the alcohols

ORGANIC - CLUTCH CH ALDEHYDES AND KETONES: NUCLEOPHILIC ADDITION

10. Alkyl Halides. What Is an Alkyl Halide. An organic compound containing at least one carbonhalogen

Chapter 8: Ethers and Epoxides. Diethyl ether in starting fluid

Organic Chemistry. M. R. Naimi-Jamal. Faculty of Chemistry Iran University of Science & Technology

Carbonyl groups react via nucleophilic addition, with the mechanism being represented as follows:

Chapter 12. Alcohols from Carbonyl Compounds Oxidation-Reduction & Organometallic Compounds. Structure

Identifying Functional Groups. Why is this necessary? Alkanes. Why is this so important? What is a functional group? 2/1/16

Allyl radicals are especially stable due to resonance ( and double bond switch places):

Ch 19 Aldehydes and Ketones

Organic Chemistry Lecture 2 - Hydrocarbons, Alcohols, Substitutions

ORGANIC - BROWN 8E CH INFRARED SPECTROSCOPY.

Name: Unit 3 Packet: Activation Energy, Free Radical Chain Reactions, Alkane Preparations, S N 2, E 2

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

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

Chap 11. Carbonyl Alpha-Substitution Reactions and Condensation Reactions

MCAT Organic Chemistry Problem Drill 10: Aldehydes and Ketones

Chapter 17: Alcohols and Phenols. Based on McMurry s Organic Chemistry, 7 th edition

Loudon Chapter 17 Review: Allylic/Benzylic Reactivity

CHEM 203. Final Exam December 18, This a closed-notes, closed-book exam. You may use your set of molecular models

Aryl Halides. Structure

Topic 9. Aldehydes & Ketones

Alcohol Synthesis. Dr. Sapna Gupta

Ethers. Synthesis of Ethers. Chemical Properties of Ethers

Available chemicals from the catalog (the starting sources of carbon compounds will continually decrease as we learn new reactions.

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.

DAMIETTA UNIVERSITY CHEM-103: BASIC ORGANIC CHEMISTRY LECTURE

Electrophile = electron loving = any general electron pair acceptor = Lewis acid, (often an acidic proton)

p Bonds as Electrophiles

ORGANIC - EGE 5E CH. 2 - COVALENT BONDING AND CHEMICAL REACTIVITY

Ethers can be symmetrical or not:

ORGANIC - BRUICE 8E CH MASS SPECT AND INFRARED SPECTROSCOPY

Dr. Mohamed El-Newehy

Learning Guide for Chapter 11 - Alkenes I

An unknown molecule A has 4 signals in the 1 H NMR spectrum. Which of the following corresponds to molecule A

Chem 263 March 28, 2006

KOT 222 Organic Chemistry II

MOLECULAR REPRESENTATIONS AND INFRARED SPECTROSCOPY

Ch 20 Carboxylic Acids and Nitriles

CHM 292 Final Exam Answer Key

Learning Guide for Chapter 17 - Dienes

Nuggets of Knowledge for Chapter 17 Dienes and Aromaticity Chem 2320

CHEM 203. Final Exam December 18, 2013 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

Nucleophilic Addition Reactions of Carboxylic Acid Derivatives

Loudon Chapter 23 Review: Amines Jacquie Richardson, CU Boulder Last updated 4/22/2018

acetaldehyde (ethanal)

Alkenes. Dr. Munther A. M-Ali For 1 st Stage Setudents

Ketones and Aldehydes Reading Study Problems Key Concepts and Skills Lecture Topics: Structure of Ketones and Aldehydes Structure:

Strategies for Organic Synthesis

ORGANIC - CLUTCH CH ANALYTICAL TECHNIQUES: IR, NMR, MASS SPECT

Mechanisms. . CCl2 F + Cl.

First 2-Hour Exam. By printing your name below, you pledge that

Infrared Spectroscopy: How to use the 5 zone approach to identify functional groups

ORGANIC - CLUTCH CH ANALYTICAL TECHNIQUES: IR, NMR, MASS SPECT

Nuggets of Knowledge for Chapter 12 Alkenes (II) Chem reaction what is added to the C=C what kind of molecule results addition of HX HX only

Chemistry 3720 Old Exams. Practice Exams & Keys

Chemistry 2030 Introduction to Organic Chemistry Fall Semester 2017 Dr. Rainer Glaser

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

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

Essential Organic Chemistry. Chapter 9

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

Chem 263 Nov 3, 2016

Learning Guide for Chapter 15 - Alcohols (II)

2.222 Practice Problems 2003

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!

Chapter 1 Reactions of Organic Compounds. Reactions Involving Hydrocarbons

12. Aldehydes & Ketones (text )

Downloaded from

(Neither an oxidation or reduction: Addition or loss of H +, H 2 O, HX).

Chem 263 Nov 24, Properties of Carboxylic Acids

Aldehydes and Ketones : Aldol Reactions

Amines Reading Study Problems Key Concepts and Skills Lecture Topics: Amines: structure and nomenclature

2Dstructuredrawing Chem314 Beauchamp

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

1. Radical Substitution on Alkanes. 2. Radical Substitution with Alkenes. 3. Electrophilic Addition

10. Organohalides. Based on McMurry s Organic Chemistry, 7 th edition

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

Organic Chemistry 1 CHM 2210 Exam 4 (December 10, 2001)

Table 8.2 Detailed Table of Characteristic Infrared Absorption Frequencies

Transcription:

CHEM 345 Problem Set 4 Key Grignard (RMgX) Problem Set You will be using Grignard reagents throughout this course to make carbon-carbon bonds. To use them effectively, it will require some knowledge from Chem 343. Making Grignard Reagents: Molecules containing a carbon halogen bond can be transformed into a Grignard reagent. Iodides react faster than bromides. omides react faster than chlorides. Fluorides react very slowly to form Grignards and are in general not used. omides are the most widely used because they balance good reactivity while not as high of cost as iodides. To make a Grignard reagent, simply add magnesium metal and diethyl ether to a molecule containing a carbon halogen bond. The magnesium will insert itself between the carbon halogen bond. (The actual mechanism probably involves radicals, but I will never ask for that mechanism) R X Mg R MgX Grignards are highly reactive compounds. First, and foremost, they are REALLY, REALLY STRNG BASES. D NT FRGET THIS!!!!! Grignards are essentially carbanions. They will react with acidic protons such as H s, NH s, SH s, and terminal alkynes. So, the Grignard reagent cannot have an acidic hydrogen on it. Second, they will react with carbon nitrogen or carbon oxygen pi bonds. Grignards cannot have carbonyls or nitriles. They also cannot contain epoxides. Third, they cannot have a leaving group (even a poor one like Me) attached to the same carbon or the carbon next to the halogen. Such Grignards eliminate to give alkenes or carbenes (that end up giving a mess) Examples of Bad Grignard Reagents H Me MgCl

1.) Circle the following molecules that can be made into a Grignard reagent. Cl contains an acidic proton Cl H contains an acidic proton contains a carbonyl Reactions of Grignard Reagents: In Chem 343, you learned that Grignards can react with epoxides to give alcohols. The Grignard typically attacks the less hindered side. This actually only works when a copper salt like CuCN is present and really is not the best use of a Grignard reagent. Grignards are primarily used to make carbon carbon bonds by reacting with carbonyl carbons to form alcohols. A Grignard reaction consists of two steps. The first step is reacting the Grignard reagent with a carbonyl in an inert solvent such as diethyl ether. The carbon carbon bond forming reaction happens here forming an alkoxide. The alkoxide is then protonated by a mild acid (H 3 + ) in a second step. H 3 + is a general term form an aqueous acidic workup step. It is just assumed that it is a weak or dilute answer in water. H 3 + R R R H The mechanism is straight forward. The electrons move from the carbon magnesium bond to the carbonyl carbon. The electrons from the pi bond go the oxygen which is protonated in the next step. R R H H H R H

2.) The following alcohols can be made by combining a Grignard reagent and a ketone/aldehyde followed by an aqueous acidic workup. Some can be made by multiple methods. Provide the Grignard and the appropriate electrophile. a.) 1.) Et 2 2.) H 3 + H a.) 1.) Et 2 2.) H 3 + H c.) 1.) Et 2 2.) H 3 + H d.) 1.) Et 2 2.) H 3 + H d.) 1.) Et 2 2.) H 3 + H

3.) Draw the following mechanism. Ph 1.) Et 2 2.) H 3 + H Ph H Ph Ph H H Ph H Chem 343 Review: Formation of alkyl bromides: S N 2 reaction Change alkyl alcohols into alkyl bromides. Two common reagents: H and P 3. P 3 is a selective reagent that converts H s into bromides by S N 2. The alpha carbon (carbon attached to the H) must be sp 3 hybridized and unhindered. H is less selective and can react with alkenes, alcohols, alkynes, and ethers. It should be used to convert tertiary alcohols into alkyl bromides. 4.) Circle the alcohols below that can be converted into bromides using P 3. a. b. H H tertiary alpha carbon too hindered for S N 2 H could be used here. c. H d. e. H f. H H neopentyl alpha carbon too hindered for S N 2 alpha carbon is sp 2 and not sp 3. need sp 3 alpha carbon for S N 2 reaction

5.) Fill in the boxes: P 3 Mg H 1.) 2.) H 3 + Mg, Et2 P 3 H 1.) 2.) H 3 + H H

6.) Chem 343 Review: The difference between PCC/CH 2 Cl 2 and H 2 Cr 4. (PCC generates aldehydes, but does not react with them. H 2 Cr 4 converts aldehydes to carboxylic acids). Fill in the boxes: For no detectable reaction, write NDR. Chiral molecules must be labeled as or. a. H PCC, CH 2 Cl 2 b. H H 2 Cr 4, H 2 H c. H PCC, CH 2 Cl 2 + D A deuterium behaves just like a hydrogen. D d. H H 2 Cr 4, H 2 D H

6.) continued. e. H PCC, CH 2 Cl 2 f. H H 2 Cr 4, H 2 g. H PCC, CH 2 Cl 2 NDR h. H H 2 Cr 4, H 2 NDR i. H PCC, CH 2 Cl 2 or H j. or H H 2 Cr 4 H 2 H

9.) From the NMR provided, determine the structure of the following compound. Assign the peaks Ha, Hb, Hc etc. accordingly. The NMR spectra are from the Sigma-Aldrich Corporation. Integrations are in bold below each peak. C 13 H 10

10.) From the NMR provided, determine the structure of the following compound. Assign the peaks Ha, Hb, Hc etc. accordingly. The NMR spectra are from the Sigma-Aldrich Corporation. Integrations are in bold below each peak. C 5 H 10