Domanda del libro di testo
Show how the following compounds can be prepared, using ethyne as one of the starting materials:
2. 1-phenyl-2-butyn-1-ol
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Ch. 16 - Reactions of Aldehydes and Ketones • More Reactions of Carboxylic Acid Derivatives
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
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Bruice 8th EditionCh. 16 - Reactions of Aldehydes and Ketones • More Reactions of Carboxylic Acid DerivativesProblema 13b
Bruice 8th EditionCh. 16 - Reactions of Aldehydes and Ketones • More Reactions of Carboxylic Acid DerivativesProblema 13bCapitolo 16, Problema 13b
Explain why ethyne should be alkylated before, rather than after, nucleophilic addition.
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Ethyne (C₂H₂) is a terminal alkyne, meaning it has a hydrogen atom attached to the sp-hybridized carbon. This hydrogen is relatively acidic due to the high s-character of the sp orbital, making it easier to deprotonate using a strong base like sodium amide (NaNH₂). This step generates a nucleophilic acetylide ion (C≡C⁻), which is highly reactive and can participate in alkylation reactions.
Alkylation involves the reaction of the acetylide ion with an alkyl halide (R-X) to form a new carbon-carbon bond. This reaction is an SN2 mechanism, which requires a strong nucleophile (the acetylide ion) and a primary or methyl alkyl halide to avoid steric hindrance and competing elimination reactions.
If nucleophilic addition (e.g., addition of water or other electrophiles) occurs before alkylation, the triple bond in ethyne will be converted into a double or single bond, depending on the reaction conditions. This reduces the acidity of the remaining hydrogen atoms and eliminates the ability to form the acetylide ion, which is essential for alkylation.
Additionally, nucleophilic addition products (e.g., alcohols or ketones) are less reactive toward alkylation because they lack the strong nucleophilicity of the acetylide ion. This makes it impossible to perform the alkylation step after nucleophilic addition.
Therefore, ethyne must be alkylated first to preserve the triple bond and the ability to generate the acetylide ion. Once alkylation is complete, subsequent reactions, such as nucleophilic addition, can be performed on the alkylated product.
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Nucleophilic Addition
Nucleophilic addition is a fundamental reaction in organic chemistry where a nucleophile attacks an electrophilic carbon atom, typically in carbonyl compounds. This process leads to the formation of a new bond and is crucial for synthesizing various organic molecules. Understanding this mechanism is essential for predicting the outcomes of reactions involving compounds like ethyne.
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08:27
Nucleophilic Addition
Alkylation
Alkylation refers to the introduction of an alkyl group into a molecule, often through a reaction with an alkyl halide. In the context of ethyne, alkylation can enhance the reactivity of the molecule, making it more favorable for subsequent nucleophilic addition. This step is important for controlling the structure and properties of the final product.
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03:19Sodium Alkynide Alkylation
Reactivity of Ethyne
Ethyne, or acetylene, is a highly reactive alkyne due to its triple bond, which can participate in various chemical reactions. When considering the order of reactions, alkylating ethyne first can stabilize the resulting product and create a more favorable environment for nucleophilic addition. This strategic approach maximizes the efficiency of the overall synthetic pathway.
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01:17Reactivity of Molecules
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