Textbook Question
Show how the following products might be synthesized from suitable Michael donors and acceptors.
(e)
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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 56b
Wade 9th EditionCh. 22 - Condensations and Alpha Substitutions of Carbonyl CompoundsProblem 56bChapter 22, Problem 56b
Show how the following products might be synthesized from suitable Michael donors and acceptors.
(b) 
Verified step by step guidance1
Step 1: Identify the product structure and recognize the functional groups. The product contains a cyclic ketone, a nitro group (-NO2), and a β-diketone structure. This suggests that the synthesis involves a Michael addition reaction.
Step 2: Determine the Michael donor. A β-diketone, such as acetylacetone (CH3COCH2COCH3), is a suitable Michael donor because it has acidic α-hydrogens that can be deprotonated to form an enolate ion.
Step 3: Determine the Michael acceptor. A nitroalkene, such as nitroethylene (CH2=CHNO2), is a suitable Michael acceptor because the electron-withdrawing nitro group stabilizes the negative charge formed during the addition.
Step 4: Outline the reaction mechanism. The enolate ion formed from the β-diketone attacks the β-carbon of the nitroalkene in a conjugate addition reaction. This forms a new C-C bond between the donor and acceptor.
Step 5: Cyclization and final product formation. After the Michael addition, intramolecular cyclization occurs, forming the cyclic ketone structure. Protonation and tautomerization complete the synthesis of the final product.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Michael Addition
Michael addition is a nucleophilic addition reaction where a nucleophile adds to an α,β-unsaturated carbonyl compound. In this reaction, a Michael donor, typically a compound with a nucleophilic site, attacks the electrophilic β-carbon of the unsaturated carbonyl, forming a new carbon-carbon bond. This reaction is crucial in organic synthesis for constructing complex molecules and is often used in the formation of various natural products.
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Michael Donors and Acceptors
Michael donors are compounds that possess nucleophilic sites, such as enolates or other electron-rich species, which can donate electrons during the Michael addition. Michael acceptors, on the other hand, are typically α,β-unsaturated carbonyl compounds that can accept the nucleophilic attack due to the presence of a polarized double bond. Understanding the nature of these donors and acceptors is essential for predicting the outcome of the reaction and for designing synthetic pathways.
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Synthesis Strategies in Organic Chemistry
Synthesis strategies in organic chemistry involve planning and executing a series of chemical reactions to construct a desired compound from simpler starting materials. This includes selecting appropriate reagents, reaction conditions, and understanding the mechanisms involved. In the context of the Michael addition, strategizing the choice of suitable Michael donors and acceptors is vital for achieving the target compound efficiently and selectively.
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Related Practice
Textbook Question
Show how the following products might be synthesized from suitable Michael donors and acceptors.
(c)
1245
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Textbook Question
Propose a mechanism for the conjugate addition of a nucleophile (Nuc:–) to acrylonitrile (H2C=CHCN) and to nitroethylene. Use resonance forms to show how the cyano and nitro groups activate the double bond toward conjugate addition.
735
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Textbook Question
Propose a mechanism for the conjugate addition of a nucleophile (Nuc:–) to acrylonitrile (H2C=CHCN). Use resonance forms to show how the cyano activate the double bond toward conjugate addition.
522
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Textbook Question
Show how the following products might be synthesized from suitable Michael donors and acceptors.
(a)
1323
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Textbook Question
Show how the following products might be synthesized from suitable Michael donors and acceptors.
(d)
623
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