Textbook Question
Predict the major products of the following crossed Claisen condensations.
(c)
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Ch. 22 - Condensations and Alpha Substitutions of Carbonyl Compounds
Wade9th EditionOrganic ChemistryISBN: 9780135213728
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Table of contents
- 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
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Wade 9th EditionCh. 22 - Condensations and Alpha Substitutions of Carbonyl CompoundsProblem 45a
Wade 9th EditionCh. 22 - Condensations and Alpha Substitutions of Carbonyl CompoundsProblem 45aChapter 22, Problem 45a
Show how Claisen condensations could be used to make the following compounds.
(a) 
Verified step by step guidance1
Step 1: Identify the target compound structure. The compound shown is a β-keto ester with a phenyl group attached to the carbonyl carbon. This suggests that a Claisen condensation reaction can be used to form the β-keto ester.
Step 2: Recall the Claisen condensation mechanism. It involves the reaction of two esters (or one ester and one ketone) in the presence of a strong base, typically an alkoxide, to form a β-keto ester. The base deprotonates the α-hydrogen of one ester, generating an enolate ion that attacks the carbonyl carbon of the second ester.
Step 3: Choose appropriate starting materials. To synthesize the target compound, you need an ester with a phenyl group (e.g., ethyl benzoate) and a cyclic ester (e.g., ethyl cyclopentanecarboxylate). These will undergo Claisen condensation to form the desired β-keto ester.
Step 4: Outline the reaction conditions. Mix ethyl benzoate and ethyl cyclopentanecarboxylate in the presence of a strong base, such as sodium ethoxide (NaOEt), in ethanol as the solvent. The base will generate the enolate ion from the cyclic ester, which will then attack the carbonyl carbon of ethyl benzoate.
Step 5: Describe the product formation. After the enolate ion attacks the carbonyl carbon of ethyl benzoate, a tetrahedral intermediate is formed. This intermediate collapses, expelling the ethoxide group and forming the β-keto ester product shown in the image.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Claisen Condensation
Claisen condensation is a reaction between two esters or an ester and a carbonyl compound in the presence of a strong base, leading to the formation of a β-keto ester or a β-diketone. This reaction involves the nucleophilic attack of an enolate ion on the carbonyl carbon of another ester, followed by elimination of an alcohol. Understanding this mechanism is crucial for synthesizing complex organic molecules.
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Claisen Condensation
Enolate Ion Formation
Enolate ions are formed when a strong base abstracts a proton from the alpha carbon of a carbonyl compound, resulting in a resonance-stabilized anion. This species is a key intermediate in Claisen condensation, as it acts as a nucleophile that attacks the carbonyl carbon of another ester. Mastery of enolate chemistry is essential for predicting reaction outcomes in organic synthesis.
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Cyclization in Organic Synthesis
Cyclization refers to the process of forming a cyclic compound from a linear precursor, often through intramolecular reactions. In the context of Claisen condensation, cyclization can occur when the reaction leads to the formation of a cyclic β-keto ester or diketone, as seen in the provided compound. Understanding the factors that favor cyclization, such as ring strain and sterics, is important for designing synthetic pathways.
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Related Practice
Textbook Question
Predict the major products of the following crossed Claisen condensations.
(b)
1114
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Textbook Question
Show how Claisen condensations could be used to make the following compounds.
(c)
811
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Textbook Question
Show how Claisen condensations could be used to make the following compounds.
(b)
987
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Textbook Question
Show how Claisen condensations could be used to make the following compounds.
(d)
875
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Textbook Question
Predict the major products of the following crossed Claisen condensations.
(a)
1097
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