carboxylic acids and derivatives. naming carboxylic acids starting materials for acyl derivatives...
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Carboxylic Acids and Derivatives
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Naming Carboxylic Acids Starting materials for acyl derivatives (esters, amides, and acid chlorides) Abundant in nature from oxidation of aldehydes and alcohols in
metabolism Carboxylic Acids, RCO2H If derived from open-chain alkanes, replace the terminal -e of the alkane
name with -oic acid The carboxyl carbon atom is C1
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Alternative Names
Compounds with CO2H bonded to a ring are named using the suffix -carboxylic acid
The CO2H carbon is not itself numbered in this system
Use common names for formic acid (HCOOH) and acetic acid (CH3COOH)
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Common names
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Structure and Physical Properties of Carboxylic Acids Carboxyl carbon sp2 hybridized: carboxylic acid
groups are planar with C–C=O and O=C–O bond angles of approximately 120°
Carboxylic acids form hydrogen bonds, existing as cyclic dimers held together by two hydrogen bonds
Strong hydrogen bonding causes much higher boiling points than the corresponding alcohols
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Dissociation of Carboxylic Acids
Carboxylic acids are proton donors toward weak and strong bases, producing metal carboxylate salts, RCO2
+M Carboxylic acids with more than six carbons are only
slightly soluble in water, but their conjugate base salts are water-soluble
Sodium Carboxylate
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Acidity Compared to Alcohols
Carboxylic acids are better proton donors than are alcohols (The pKa of ethanol is ~16, compared to ~5 for acetic acid)
In an alkoxide ion, the negative charge is localized on oxygen while in a carboxylate ion the negative charge is delocalized over two equivalent oxygen atoms, giving resonance stabilization
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Substituent Effects on Acidity
Electronegative substituents promote formation of the carboxylate ion
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Substituent Effects in Substituted Benzoic Acids
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Preparation of Carboxylic Acids
Oxidation of a primary alcohol or an aldehyde with CrO3 in aqueous acid
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From alkyl benzene
Oxidation of a substituted alkylbenzene with KMnO4 gives a substituted benzoic acid
1° and 2° alkyl groups can be oxidized, but tertiary groups are not
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From Alkenes
Oxidative cleavage of an alkene with KMnO4 gives a carboxylic acid if the alkene has at least one vinylic hydrogen
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Hydrolysis of Nitriles
Hot acid yields carboxylic acids Conversion of an alkyl halide to a nitrile (with cyanide
ion) followed by hydrolysis produces a carboxylic acid with one more carbon (RBr RCN RCO2H)
Best with primary or secondary halides because tertiary alkyl halides are sterically hindered
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Carboxylation of Grignard Reagents
Grignard reagents react with dry CO2 to yield a metal carboxylate
Limited to alkyl halides that can form Grignard reagents
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Mechanism of Grignard Carboxylation
The organomagnesium halide adds to C=O of carbon dioxide
Protonation by addition of aqueous HCl in a separate step gives the free carboxylic acid
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Reactions of Carboxylic Acids: An Overview Carboxylic acids transfer a proton to a base to give
anions, which are good nucleophiles in SN2 reactions Like ketones, carboxylic acids undergo addition of
nucleophiles to the carbonyl group In addition, carboxylic acids undergo other reactions
characteristic of neither alcohols nor ketones
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Reduction of Carboxylic Acids
Reduced by LiAlH4 to yield primary alcohols The reaction is difficult and often requires heating in
tetrahydrofuran solvent to go to completion
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Reduction with Borane
Borane in tetrahydrofuran (BH3/THF) converts carboxylic acids to primary alcohols selectively
Preferable to LiAlH4 because of its relative ease, safety, and specificity
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Nucleophilic Acyl Substitution
Carboxylic acid derivatives have an acyl carbon bonded to a group Y that can leave
A tetrahedral intermediate is formed and the leaving group is expelled to generate a new carbonyl compound, leading to substitution
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Carboxylic acid derivatives
Acyl group bonded to X, an electronegative atom or leaving group
Includes: X = halide (acid halides), acyloxy (anhydrides), alkoxy (esters), amine (amides), thiolate (thioesters)
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Naming Carboxylic Acid Derivatives Acid Halides, RCOX
Derived from the carboxylic acid name by replacing the -ic acid ending with -yl or the -carboxylic acid ending with –carbonyl and specifying the halide
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Naming Acid Anhydrides, RCO2COR'
If symmetrical replace “acid” with “anhydride” based on the related carboxylic acid
Unsymmetrical anhydrides— cite the two acids alphabetically
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Naming Amides, RCONH2
With unsubstituted NH2 group. replace -oic acid or -ic acid with -amide, or by replacing the -carboxylic acid ending with –carboxamide
If the N is further substituted, identify the substituent groups (preceded by “N”) and then the parent amide
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Naming Esters, RCO2R’
Name R’ and then, after a space, the carboxylic acid (RCOOH), with the “-ic acid” ending replaced by “-ate”
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Name the following compounds
4-methylpentanoyl Chloride Cylopentyl 2-methylpropanoate
Isopropyl Cyclopentanecarboxylate
Isopropyl 2-methylpropanoate
2-Cylcohexyl Acetamide
N-Methyl-4-pentenamide
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Relative Reactivity of Carboxylic Acid Derivatives Nucleophiles react
more readily with unhindered carbonyl groups
More electrophilic carbonyl groups are more reactive to addition (acyl halides are most reactive, amides are least)
The intermediate with the best leaving group decomposes fastest