Organic Chemistry,5th Edition L.G.Wade,Jr. Chapter 20 Carboxylic Acids Jo Blackburn Richland College,Dallas,TX Dallas County Community College District ©2003，Prentice Hall
Chapter 20 Carboxylic Acids Jo Blackburn Richland College, Dallas, TX Dallas County Community College District © 2003, Prentice Hall Organic Chemistry, 5th Edition L. G. Wade, Jr
Introduction The functional group of carboxylic acids consists of a C=O with -OH bonded to the same carbon. Carboxyl group is usually written -COOH. Aliphatic acids have an alkyl group bonded to -COOH. Aromatic acids have an aryl group. Fatty acids are long-chain aliphatic acids. > Chapter 20
Chapter 20 2 Introduction • The functional group of carboxylic acids consists of a C=O with -OH bonded to the same carbon. • Carboxyl group is usually written -COOH. • Aliphatic acids have an alkyl group bonded to -COOH. • Aromatic acids have an aryl group. • Fatty acids are long-chain aliphatic acids. =>
Common Names Many aliphatic acids have historical names. Positions of substituents on the chain are labeled with Greek letters. -C-C-C-C一C-C OH 8 Ph CI O CH:CH2CH2CHCH2COOH CH3CH2CHC-OH β-phenylcaproic acid a-chlorobutyric acid Chapter 20 3 =>
Chapter 20 3 Common Names • Many aliphatic acids have historical names. • Positions of substituents on the chain are labeled with Greek letters. CH3 CH2 CHC Cl OH O -chlorobutyric acid CH3 CH2 CH2 CHCH2 COOH Ph -phenylcaproic acid =>
IUPAC Names Remove -e from alkane(or alkene) name,add -oic acid. The carbon of the carboxyl group is #1. CIO H CH:CH-CHC-OH Ph-c=C H COOH 2-chlorobutanoic acid trans-3-phenyl-2-propenoic acid (cinnamic acid) => Chapter 20
Chapter 20 4 IUPAC Names • Remove -e from alkane (or alkene) name, add -oic acid. • The carbon of the carboxyl group is #1. CH3 CH2 CHC Cl OH O 2-chlorobutanoic acid Ph C H C H COOH trans-3-phenyl-2-propenoic acid (cinnamic acid) =>
Naming Cyclic Acids Cycloalkanes bonded to -COOH are named as cycloalkanecarboxylic acids. Aromatic acids are named as benzoic acids. COOH COOH CH(CH3)2 OH 2-isopropylcyclopentanecarboxylic acid -hydroxybenzoic acid (salicylic acid) => Chapter 20 5
Chapter 20 5 Naming Cyclic Acids • Cycloalkanes bonded to -COOH are named as cycloalkanecarboxylic acids. • Aromatic acids are named as benzoic acids. COOH CH(CH3 ) 2 2-isopropylcyclopentanecarboxylic acid COOH OH o-hydroxybenzoic acid (salicylic acid) =>
Dicarboxylic Acids Aliphatic diacids are usually called by their common names (to be memorized). For IUPAC name,number the chain from the end closest to a substituent. Two carboxyl groups on a benzene ring indicate a phthalic acid. Br HOOCCH2CHCH2CH2COOH 3-bromohexanedioic acid B-bromoadipic acid Chapter 20 6
Chapter 20 6 Dicarboxylic Acids • Aliphatic diacids are usually called by their common names (to be memorized). • For IUPAC name, number the chain from the end closest to a substituent. • Two carboxyl groups on a benzene ring indicate a phthalic acid. HOOCCH2 CHCH2 CH2 COOH Br 3-bromohexanedioic acid -bromoadipic acid =>
Structure of Carboxyl Carbon is sp2 hybridized. ·Bond angles are close to120°. ·O-H eclipsed with C=O,to get overlap ofπ orbital with orbital of lone pair on oxygen. :O major very minor minor Chapter 20
Chapter 20 7 Structure of Carboxyl • Carbon is sp2 hybridized. • Bond angles are close to 120. • O-H eclipsed with C=O, to get overlap of orbital with orbital of lone pair on oxygen. =>
Boiling Points Higher boiling points than similar alcohols, due to dimer formation. ∠0H-0 R C- R 0-H…0 hydrogen-bonded acid dimer Acetic acid,b.p.118C 二> Chapter 20 8
Chapter 20 8 Boiling Points Higher boiling points than similar alcohols, due to dimer formation. Acetic acid, b.p. 118C =>
Melting Points Aliphatic acids with more than 8 carbons are solids at room temperature. Double bonds (especially cis)lower the melting point.Note these 18-C acids: >Stearic acid (saturated):72C >Oleic acid (one cis double bond):16C >Linoleic acid (two cis double bonds):-5C => Chapter 20 9
Chapter 20 9 Melting Points • Aliphatic acids with more than 8 carbons are solids at room temperature. • Double bonds (especially cis) lower the melting point. Note these 18-C acids: ➢Stearic acid (saturated): 72C ➢Oleic acid (one cis double bond): 16C ➢Linoleic acid (two cis double bonds): -5C =>
Solubility Water solubility decreases with the length of the carbon chain. Up to 4 carbons,acid is miscible in water. More soluble in alcohol. Also soluble in relatively nonpolar solvents like chloroform because it dissolves as a dimer. => Chapter 20 10
Chapter 20 10 Solubility • Water solubility decreases with the length of the carbon chain. • Up to 4 carbons, acid is miscible in water. • More soluble in alcohol. • Also soluble in relatively nonpolar solvents like chloroform because it dissolves as a dimer. =>