《大学化学》课程PPT教学课件（英文版讲稿）Chapter 12 Organic Chemistry

Organic Chemistry Chapter 12 Copyright o The McGraw-Hill Companies, Inc. Permission required for reproduction or display

Organic Chemistry Chapter 12 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display

Carbon atoms have the ability to link together and form molecules made up of many carbon atoms The branch of chemistry that is the study of carbon-containing compounds is known as organic chemistry(有机化学) 13 million known organic compounds and 100,000 new ones are added annually Only 200,000-300,000 known inorganic compounds

• Carbon atoms have the ability to link together and form molecules made up of many carbon atoms. • The branch of chemistry that is the study of carbon-containing compounds is known as organic chemistry (有机化学). • 13 million known organic compounds and 100,000 new ones are added annually. • Only 200,000-300,000 known inorganic compounds

121 Hydrocarbons(碳氢化合物、烃) contain only carbon and hydrogen Hydrocarbons differ from each other by the number of carbon atoms methane cH4 Octane C8H18 polyethylene

12.1 Hydrocarbons (碳氢化合物、烃) contain only carbon and hydrogen • Hydrocarbons differ from each other by the number of carbon atoms. methane CH4 Octane C8H18 polyethylene

Hydrocarbons differ from each other also by the way carbon atoms connect to each other. Straight-chain hydrocarbon, branched hydrocarbon Molecules having the same chemical formula but different structures are called structural isomers(结构异构体). Structural isomers have different physical and chemical properties. The number of possible structural isomers for a chemical formula increases rapidly as the number of carbon atoms increases: 3 for CeH, 18 for Coha. 75 for C10H22366,319forC20H c624e 33● HHHH H H CH3H H H CH3 H H-C-C-C-C-C-HHCC-C一C一H HC-C-C—H HHHH H CH3 H n-pentane ISo-pentane Neo- pentane

• Hydrocarbons differ from each other also by the way carbon atoms connect to each other. Straight-chain hydrocarbon, branched hydrocarbon • Molecules having the same chemical formula but different structures are called structural isomers (结构异构体). Structural isomers have different physical and chemical properties. The number of possible structural isomers for a chemical formula increases rapidly as the number of carbon atoms increases: 3 for C5H12, 18 for C8H18, 75 for C10H22, 366,319 for C20H42. n-pentane iso-pentane Neo- pentane C H H H C C C C H H H H H H H H H C H H H C C C H CH3 H H H H H C H H H C C H CH3 CH3 H H

Carbon-based molecules can have different spatial orientations called conformations(构象) Fig 12.2 three conformation for a molecule of n-pentane. the molecule looks different in each conformation but the five-carbon framework is the same in all three conformations In a sample of liquid n-pentane the molecules are found in all conformations-not unlike a bucket of worms

Carbon-based molecules can have different spatial orientations called conformations (构象). Fig12.2 three conformation for a molecule of n-pentane. The molecule looks different in each conformation, but the five-carbon framework is the same in all three conformations. In a sample of liquid n-pentane, the molecules are found in all conformations- not unlike a bucket of worms

Hydrocarbons are usually from crude oil by fractional distillation(分馏) Gas Gasoline Fig 12.3 a 30°c-180°c schematic for Naphtha the fractional 110°c-195°c distillation of → Kerosene petroleum into 170c-290°C its useful hydrocarbon → Heating oil components 260°C-350°c Lubricating oil Heated 300°c-370°c crude oil at370°c → Residue

Hydrocarbons are usually from crude oil by fractional distillation (分馏). Fig12.3 a schematic for the fractional distillation of petroleum into its useful hydrocarbon components

122 Unsaturated hydrocarbons(不饱和烃) contain multiple bonds saturated hydrocarbon Unsaturated hydrocarbon CH3-CH2-CH2-CH3 CH3 CH=CH--CH3 n-butane 2-butene

12.2 Unsaturated hydrocarbons (不饱和烃) contain multiple bonds CH3 CH CH CH3 2-butene saturated hydrocarbon Unsaturated hydrocarbon CH3－CH2－ CH2 － CH3 n-butane

Benzene(苯) and aromatic compounds(芳香化合物) Fig 12.8 (a) the double bonds of benzene, C6H6, are able to migrate around the ring. (b) for this reason, they are often represented by a circle within the ring

Benzene (苯) and aromatic compounds (芳香化合物) Fig 12.8 (a) the double bonds of benzene, C6H6, are able to migrate around the ring. (b) for this reason, they are often represented by a circle within the ring (a) (b)

toluene naphthalene 1. 4-dichlorobenzene

toluene naphthalene 1,4-dichlorobenzene Cl Cl

12. 3 Organic molecules are classified by functional group(官能团) N Important Functional Groups and Their Reactions ·醇、酚、醚、豆 W Functional Group Name Typical Reactions Carbon-carbon Addition reactions with halogens 胺、酮、醛、 double bond hydrogen halides, and water: with hal 酰胺、羧酸、 triple bond hydrogen halides; hydrogenation to yield alkenes and alkanes 酯 halogen Exchange reactions (X=F, CL, Br, D CHCH,Br+K CHCH,I+ KBr 0-H Hydroxyl Esterification(formation of an ester) with carboxylic acids; oxidation to aldehydes, ketones, and carboxylic acids Reduction to yield alcohols, oxidation 4 o of aldehydes to yield carboxylic acids Carboxyl Esterification with alcohols: reaction with phosphorus pentachloride to yield acid chlorides :O: -O-R Ester Hydrolysis to yield acids and alcohols (R= hydrocarbon) An Formation of ammonium salts with (R= H or hydrocarbon)

12.3 Organic molecules are classified by functional group (官能团) • 醇、酚、醚、 胺、酮、醛、 酰胺、羧酸、 酯