Objective. Reactions of Haloalkanes with metals When a solution of an alkyl halide in dry ether is treated with magnesium, an alkyl magnesium halide is.

Slides:



Advertisements
Similar presentations
10. Organohalides Based on McMurry’s Organic Chemistry, 7 th edition.
Advertisements

Oxidation-Reduction & Organometallic
1 2 ALKYL HALIDES – ELIMINATION REACTIONS ALKYL HALIDES UNDERGO ELIMINATION OF HX WHEN TREATED WITH BASE. THE PRODUCTS.
Chapter 10. Alkyl Halides. What Is an Alkyl Halide An organic compound containing at least one carbon-halogen bond (C-X) –X (F, Cl, Br, I) replaces H.
10. Alkyl Halides Based on McMurry’s Organic Chemistry, 6 th edition.

15-1 Organometallic Compounds Chapter Organometallic Compounds  Organometallic compound:  Organometallic compound: A compound that contains.
Chemistry 2412L Grignard Reaction Pre-lab lecture.
Synthesis of Alcohols Reduction of Aldehydes and Ketones Common reducing agents and conditions: NaBH 4 ( sodium borohydride ) alcohol, ether, or H 2 O.
Compounds that contain _________________bond (______): Examples of M include ________(Grignard reagents), _____________. ____________ carbon: Reacts with.
Chapter 8: Ethers and Epoxides Diethyl ether in starting fluid.
Your Questions ?? α-bromoethylbenzene Answers to MiniQuiz 4: α-dibromoethylbenzene: one singlet and groups of aromatics Quartet 1:3:3:1 ! Score: 2*/2.
Alcohols: Structure & Synthesis
MiniQuiz 3 Problem: Draw a rough (but clear) H-NMR of a sample that contains (only)  -monobromoethyl benzene in CCl 4.
Organometallic Reagents: Sources of Nucleophilic Carbon for Alcohol Synthesis 8-7 If the carbonyl carbon of an aldehyde or ketone could be attacked by.
WWU -- Chemistry REAGENTS WITH CARBON- METAL BONDS; ORGANOMETALLIC SYNTHESIS OF ALCOHOLS Chapter 15.
Chapter 14 Organometallic Compounds
Chemistry 2412L Grignard Reaction Pre-lab lecture.
Chapter 14 Organometallic Compounds Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Chapter 14: Organometallics, structure and nomenclature.
Dr Manal F. AbouTaleb Alkanes 1 Introduction 2 Nomenclature of Alkanes
Ethers & Epoxides. Ether Nomenclature Compounds that contain two organic groups attached to an oxygen atom General formula is 1. Common Names – Name both.
Objective. Reactions of Haloarenes with metals When the magnesium metal reacts with bromobenzene and iodobenzene in presence of ether to form Grignard.
Ethers Nanoplasmonic Research Group Organic Chemistry Chapter 8 Part I.
Chapter 15 Reagents with Carbon-Metal Bonds
1 FIVE METHODS OF PREPARING ALCOHOLS. 2 5 METHODS OF PREPARING ALCOHOLS 1. Hydroxide ions (OH - ) replace halogens in unhindered alkyl halides (Me° and.
Renee Y. Becker CHM 2210 Valencia Community College
John E. McMurry Paul D. Adams University of Arkansas Chapter 10 Organohalides.
Reactions of Oxacyclopropanes 9-9 Nucleophilic ring opening of oxacyclopropanes by S N 2 is regioselective and stereospecific. Oxacyclopropane can be ring-opened.
Learning Objectives Preparation of alcohols Intermolecular dehydration
VIDEO EXAMPLE OF SUBSTITUTION The hydrolysis of t-butyl halides They’re often easy/fast (facile) Done at room.
Study the target molecule and the list of available reagents. CH 12-4: Performing a Grignard Synthesis-II From the reagent list (stockroom) identify the.
Preparation of Alkanes Methane through -pentane and iso-pentane can be obtained in pure form by fractional distillation of petroleum and natural gas; neo-pentane.
John E. McMurry Paul D. Adams University of Arkansas Chapter 10 Organohalides.
Organometallic Reagents: Sources of Nucleophilic Carbon for Alcohol Synthesis 8-7 If the carbonyl carbon of an aldehyde or ketone could be attacked by.
10. Alkyl Halides. 2 What Is an Alkyl Halide An organic compound containing at least one carbon- halogen bond (C-X) X (F, Cl, Br, I) replaces H Can contain.
John E. McMurry Paul D. Adams University of Arkansas Chapter 10 Organohalides.
Alkane Reactions. t Alkanes have only single, covalent, non- polar bonds Alkanes are relatively inert to most chemical reagents Alkanes are also called.
© 2016 Cengage Learning. All Rights Reserved. John E. McMurry Chapter 10 Organohalides.
Ch. 7 Alcohols and Phenols BY MAHWASH HAFEEZ. General Formulas and Functional Groups Both of these families contain a hydroxyl group (OH) as functional.
Chapter 2 ALKANES Dr. Yasser Mostafa
Grignard’s reagents understand methods of increasing the length of the carbon chain in a molecule by the use of magnesium to form Grignard reagents and.
Organic Halogen Compounds
Oxidation-Reduction & Organometallic
Chapter 14 Organometallic Compounds
Organometallic Compounds
Chemistry Department, College of Science, King Saud University
Chapter 10 Organohalides
Chapter 10 Organohalides
Chapter 10 Organohalides
Chapter 10 Organohalides
Organomettalic Chemistry Y. B. Chavan College of Pharmacy
Chapter 10 Organohalides.
CH 12-3: Grignard Reaction-I
Chapter 10 Organohalides
Preparation Reactions of Alkanes
ALKANES.
Organometallic Compounds
Preparation of alkanes
Chapter 20 Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction.
Based on McMurry’s Organic Chemistry, 7th edition
Based on McMurry’s Organic Chemistry, 7th edition
Organ metallic Compounds
GRIGNARDS REAGENT NEW CHAPTER R-Mg-X.
10. Alkyl Halides Based on McMurry’s Organic Chemistry, 6th edition
GRIGNARDS REAGENT NEW CHAPTER R-Mg-X.
Based on McMurry’s Organic Chemistry, 7th edition
Chapter 10 Organohalides
Synthesis, Properties and Reactions of Alkanes
GRIGNARD’S REAGENT R-Mg-X.
Presentation transcript:

Objective

Reactions of Haloalkanes with metals When a solution of an alkyl halide in dry ether is treated with magnesium, an alkyl magnesium halide is formed. Alkyl magnesium halides, generally, represented as RMgX, are known as Grignard reagents.

Action with Sodium Two molecules of alkyl halides (same or different) react with metallic sodium in the presence of ether to form alkanes. This reaction is called Wurtz reaction and is used to prepare symmetrical alkanes.

Reaction with other Active Metals Haloalkanes react with other active metals such as lithium, zinc, mercury, lead, etc. in the presence of dry ether to form the corresponding organometallic compounds. For example,