'Alkyl group' diaporamas de présentation

CHAPTER 8 INTRODUCTION TO ORGANIC CHEMISTRY

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Chapter 22

Chapter 22. Introduction to General, Organic, and Biochemistry, 10e John Wiley & Sons, Inc Morris Hein, Scott Pattison, and Susan Arena. Alcohols, Ethers, Phenols, and Thiols. This field of switch grass is a prime source of biomass for ethanol production. 22.1 Functional Groups

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Esters

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FATS

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11.11 The Birch Reduction

11.11 The Birch Reduction. Dr. Wolf's CHM 201 & 202. H. H. H. H. H. H. H. H. H. H. H. H. H. H. Birch Reduction of Benzene. Product is non-conjugated diene. Reaction stops here. There is no further reduction. Reaction is not hydrogenation. H 2 is not involved in any way. .

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Chem 51, Exam 1. October 13, 2009

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Reactions of Benzene and its Derivatives

Reactions of Benzene and its Derivatives. Chapter 22. Chapter 22. Reactions of Benzene. The most characteristic reaction of aromatic compounds is substitution at a ring carbon. This is Electrophilic Aromatic Substitution (EAS) . Sulfonation:. H. S. O. 2. 4. S. O. S. O. H. 3. 3.

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Chemistry 20

Chemistry 20. Unit 3 Part 5 Nomenclature. Nomenclature. IUPAC Naming System (Nomenclature) IUPAC = __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ __ abcdefghijklmnopqrstuvqxyz. Nomenclature (Ionic).

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Ch 22: Organic Chemistry

Ch 22: Organic Chemistry. Section 1: Organic Compounds. Organic Compounds : covalently bonded compounds containing carbon, excluding carbonates and oxides. Carbon is unique in that its electronic structure allows it: to bind to itself to form chains and rings

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Chemistry

Chemistry. Session - 2. Carboxylic Acids. Session Objectives. Introduction to carboxylic acids Physical properties and structure General method of preparation By oxidation Carbonation of grignard reagent Hydrolysis of acid derivatives From nitriles

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Alcohols and ethers

Alcohols and ethers. Structure. R-OH alcohol R = alkyl group (substituted or unsubstituted). Sterols - the steroid ring system. Physical properties of alcohols.

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Organic reaction mechanisms

Organic reaction mechanisms. Click a box below to go to the mechanism. Click here for advice. Homolytic. Free Radical Substitution. Free Radical Addition. Heterolytic. Electrophilic Addition. S N 2. S N 1. Nucleophilic Substitution. Nitration. Br 2. Electrophilic Substitution.

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Organic Chemistry

Organic Chemistry. Brown, LeMay Ch 25 AP Chemistry Monta Vista High School. Problem Set: #5, 7, 9, 10, 11, 15, 20, 23 (not c), 41(not c), 44; Recommended: #2, 16, 17, 43, 69. 25.1: Organic Chemistry. The study of carbon compounds, but not limited to living systems

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Organic Functional Groups

Organic Functional Groups. What is a functional Group?. Element, Compound, or entire chain that replaces a hydrogen on a hydrocarbon chain Alter the properties of the original hydrocarbon Create a new molecule with unique properties

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STER

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medicines and drugs

medicines and drugs. a ntibacterials. Diseases caused by bacteria. tuberculosis, syphilis, cholera, salmonella, bronchitis, anthrax, meningitis, gonorrhea, chlamydia . antibacterials.

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Dr. Pandit Khakre Asst. Prof Mrs. K.S.K. College, Beed

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Reactions for Exam (you will have the reducing agent chart on exam) :

Reactions for Exam (you will have the reducing agent chart on exam) : Everything from 241a ( epoxidation s , halides from alcohols, ether synthesis) Electrophilic substitution reactions: bromination & chlorination* iodination nitration* sulfonation *

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