Domanda del libro di testo
Indicate how the following compounds can be synthesized from cyclohexanone and any other necessary reagents:
d.
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Ch. 17 - Reactions at the Alpha-Carbon
Bruice8th EditionOrganic ChemistryISBN: 9780135213711
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TOC.tableOfContents
- Ch. 1 - Remembering General Chemistry: Electronic Structure and Bonding31
- Ch. 2 - Acids and Bases: Central to Understanding Organic Chemistry84
- Ch. 3 - An Introduction to Organic Compounds: Nomenclature, Physical Properties, and Structure183
- Ch. 4 - Isomers: The Arrangement of Atoms in Space121
- Ch. 5 - Alkenes: Structure, Nomenclature, and an Introduction to Reactivity • Thermodynamics and Kinetics83
- Ch. 6 - The Reactions of Alkenes • The Stereochemistry of Addition Reactions175
- Ch. 7 - The Reactions of Alkynes • An Introduction to Multistep Synthesis119
- Ch. 8 - Delocalized Electrons: Their Effect on Stability, pKa, and the Products of a Reaction • Aromaticity and Electronic Effects: An Introduction to the Reactions of Benzene148
- Ch. 9 - Substitution and Elimination Reactions of Alkyl Halides212
- Ch. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing Compounds131
- Ch. 11 - Organometallic Compounds60
- Ch. 12 - Radicals90
- Ch. 13 - Mass Spectrometry; Infrared Spectroscopy; UV/Vis Spectroscopy62
- Ch. 14 - NMR Spectroscopy95
- Ch. 15 - Reactions of Carboxylic Acids and Carboxylic Acid Derivatives123
- Ch. 16 - Reactions of Aldehydes and Ketones • More Reactions of Carboxylic Acid Derivatives141
- Ch. 17 - Reactions at the Alpha-Carbon101
- Ch. 18 - Reactions of Benzene and Substituted Benzenes144
- Ch. 19 - More About Amines • Reactions of Heterocyclic Compounds49
- Ch. 20 - The Organic Chemistry of Carbohydrates80
- Ch. 21 - Amino Acids, Peptides, and Proteins57
- Ch. 22 - Catalysis in Organic Reactions and in Enzymatic Reactions35
- Ch. 23 - The Organic Chemistry of the Coenzymes—Compounds Derived from Vitamins1
- Ch. 28 - Pericyclic Reactions58
Capitolo 17, Problema 67c
The Reformatsky reaction is an addition reaction in which an organozinc reagent is used instead of a Grignard reagent to add to the carbonyl group of an aldehyde or a ketone. Because the organozinc reagent is less reactive than a Grignard reagent, a nucleophilic addition to the ester group does not occur.
The organozinc reagent is prepared by treating an α-bromo ester with zinc.
Describe how each of the following compounds can be prepared, using a Reformatsky reaction:
c. 
Guida verificata passo dopo passo1
Identify the target compound that needs to be synthesized using the Reformatsky reaction. This will typically involve recognizing the carbonyl compound (aldehyde or ketone) and the ester that will form the organozinc reagent.
Determine the structure of the alpha-bromo ester needed to form the organozinc reagent. The alpha-bromo ester should have the same carbon skeleton as the desired product, minus the carbonyl group.
React the alpha-bromo ester with zinc metal to form the organozinc reagent. This step involves the insertion of zinc into the carbon-bromine bond, creating a nucleophilic organozinc species.
Perform the nucleophilic addition of the organozinc reagent to the carbonyl compound (aldehyde or ketone). This step involves the organozinc reagent attacking the electrophilic carbon of the carbonyl group, forming a new carbon-carbon bond.
Finally, perform a workup step, typically involving the addition of an acid, to protonate the alkoxide intermediate and yield the desired beta-hydroxy ester product.
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Reformatsky Reaction
The Reformatsky reaction is a chemical reaction that involves the addition of an organozinc reagent to a carbonyl compound, typically an aldehyde or ketone. This reaction is notable for using organozinc reagents, which are less reactive than Grignard reagents, allowing for selective reactions without unwanted side reactions, such as nucleophilic addition to esters.
Video consigliato:
05:09
Heck Reaction
Organozinc Reagents
Organozinc reagents are organometallic compounds that contain a carbon-zinc bond. They are generally less reactive than Grignard reagents, making them useful in reactions where controlled reactivity is desired. These reagents are typically prepared by reacting zinc with alkyl or aryl halides, such as a-bromo esters, which are crucial for the Reformatsky reaction.
Video consigliato:
01:52Reagents
Nucleophilic Addition
Nucleophilic addition is a fundamental reaction mechanism in organic chemistry where a nucleophile attacks an electrophilic carbon atom, typically in a carbonyl group. In the context of the Reformatsky reaction, the reduced reactivity of organozinc reagents prevents unwanted nucleophilic addition to ester groups, allowing for more selective reactions with aldehydes and ketones.
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08:27Nucleophilic Addition
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Indicate how each of the following compounds can be synthesized from the given starting material and any other necessary reagents:
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