Domanda del libro di testo
Show how to synthesize the following compounds, using appropriate carboxylic acids and amines.
(b)
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Ch. 20 - Carboxylic Acids
Wade9th EditionOrganic ChemistryISBN: 9780135213728
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TOC.tableOfContents
- Ch.1 - Structure and Bonding107
- Ch. 2 - Acids and Bases; Functional Groups115
- Ch.3 - Structure and Stereochemistry of Alkanes100
- Ch.4 - The Study of Chemical Reactions99
- Ch.5 - Stereochemistry93
- Ch.6 - Alkyl Halides; Nucleophilic Substitution118
- Ch. 7 - Structure and Synthesis of Alkenes; Elimination158
- Ch.8 - Reactions of Alkenes171
- Ch.9 - Alkynes91
- Ch.10 - Structure and Synthesis of Alcohols143
- Ch.11 - Reactions of Alcohols104
- Ch. 12 - Infrared Spectroscopy and Mass Spectrometry22
- Ch. 13 - Nuclear Magnetic Resonance Spectroscopy45
- Ch. 14 - Ethers, Epoxides, and Thioethers72
- Ch. 15 - Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy89
- Ch. 16 - Aromatic Compounds74
- Ch. 17 - Reactions of Aromatic Compounds126
- Ch. 18 - Ketones and Aldehydes193
- Ch. 19 - Amines129
- Ch. 20 - Carboxylic Acids77
- Ch. 21 - Carboxylic Acid Derivatives141
- Ch. 22 - Condensations and Alpha Substitutions of Carbonyl Compounds175
- Ch. 23 - Carbohydrates and Nucleic Acids93
- Ch. 24 - Amino Acids, Peptides, and Proteins54
Capitolo 20, Problema 18a
Show how to synthesize the following compounds, using appropriate carboxylic acids and amines.
(a) 
Guida verificata passo dopo passo1
Step 1: Identify the functional groups in the target molecule, DEET. It contains an amide functional group (-CONR2) attached to a benzene ring with a methyl substituent in the meta position.
Step 2: Select the appropriate carboxylic acid precursor. The carboxylic acid should have the benzene ring with a methyl group in the meta position relative to the carboxylic acid group. This compound is meta-toluic acid (C8H8O2).
Step 3: Choose the amine precursor. The amine required is diethylamine (CH3CH2)2NH, as the amide group in DEET contains two ethyl groups attached to the nitrogen atom.
Step 4: Perform the synthesis reaction. React meta-toluic acid with diethylamine in the presence of a dehydrating agent such as dicyclohexylcarbodiimide (DCC) or by using acid chloride formation followed by amine addition. This will result in the formation of the amide bond.
Step 5: Purify the product. Use techniques such as recrystallization or chromatography to isolate and purify the synthesized DEET compound.
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Carboxylic Acids
Carboxylic acids are organic compounds characterized by the presence of a carboxyl group (-COOH). They are important in organic synthesis as they can react with amines to form amides. Understanding the reactivity and properties of carboxylic acids is crucial for synthesizing compounds like DEET, where the carboxylic acid serves as a precursor in the formation of the amide bond.
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04:20
Carboxylic Acids Nomenclature
Amines
Amines are organic compounds derived from ammonia by replacing one or more hydrogen atoms with alkyl or aryl groups. They can act as nucleophiles in chemical reactions, particularly in the formation of amides from carboxylic acids. In the synthesis of DEET, the amine component is essential for creating the desired structure and functionality of the insect repellent.
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07:12Reductive Amination
Amide Formation
Amide formation is a key reaction in organic chemistry where a carboxylic acid reacts with an amine to produce an amide and water. This reaction is significant in the synthesis of various compounds, including pharmaceuticals and agrochemicals. In the case of DEET, understanding the mechanism of amide formation helps in designing the synthesis pathway and optimizing reaction conditions.
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01:33Amide Nomenclature
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Show how you would synthesize the following compounds from the appropriate carboxylic acids or acid derivatives.
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The mechanism of the Fischer esterification was controversial until 1938, when Irving Roberts and Harold Urey of Columbia University used isotopic labeling to follow the alcohol oxygen atom through the reaction. A catalytic amount of sulfuric acid was added to a mixture of 1 mole of acetic acid and 1 mole of special methanol containing the heavy 18O isotope of oxygen. After a short period, the acid was neutralized to stop the reaction, and the components of the mixture were separated.
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The given was missing some important resonance forms of the intermediates shown in brackets. Complete this mechanism by drawing all the resonance forms of these intermediates. Do your resonance forms help to explain why this reaction occurs under very mild conditions (water with a tiny trace of acid)?
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Show how to synthesize the following compounds, using appropriate carboxylic acids and amines.
(c)
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