Domanda del libro di testo
Predict the products formed when the following sugars react with excess acetic anhydride and pyridine.
(a) α-D-glucopyranose
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Ch. 23 - Carbohydrates and Nucleic 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 23, Problema 28b
Predict the products formed when the following sugars react with excess acetic anhydride and pyridine.
(b) β-D-ribofuranose
Guida verificata passo dopo passo1
Identify the functional groups present in β-D-ribofuranose. It contains hydroxyl (-OH) groups on the sugar ring and a hemiacetal group at the anomeric carbon.
Understand the role of acetic anhydride and pyridine. Acetic anhydride is an acetylating agent that reacts with hydroxyl groups to form acetate esters, while pyridine acts as a base to neutralize the byproduct (acetic acid) and facilitate the reaction.
Determine the reaction sites. In β-D-ribofuranose, all hydroxyl groups (including the one at the anomeric carbon) will react with acetic anhydride to form acetate esters. The hemiacetal group at the anomeric carbon will also be acetylated.
Write the structure of the product. Replace each hydroxyl group (-OH) in β-D-ribofuranose with an acetate group (-OCOCH₃). Ensure that the stereochemistry of the sugar is preserved during the substitution.
Verify the final product. The product will be a fully acetylated derivative of β-D-ribofuranose, where all hydroxyl groups are converted to acetate esters, and the sugar retains its furanose ring structure.
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Acetic Anhydride Reactivity
Acetic anhydride is a powerful acetylating agent commonly used in organic chemistry to introduce acetyl groups into alcohols and sugars. When sugars react with acetic anhydride, the hydroxyl groups (-OH) on the sugar molecules are converted into acetyl groups (-OCOCH3), resulting in the formation of acetylated sugars. This reaction is important for modifying the solubility and reactivity of sugars.
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03:35
Anhydride Nomenclature
Pyridine as a Catalyst
Pyridine is often used as a base in organic reactions, including acetylation processes. It helps to deprotonate the hydroxyl groups of sugars, making them more nucleophilic and thus more reactive towards acetic anhydride. This catalytic role enhances the efficiency of the acetylation reaction, facilitating the formation of the acetylated products.
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Percorso guidato
2:10Introduction to Catalysis Concept 1
Sugar Structure and Reactivity
The structure of sugars, such as b-D-ribofuranose, influences their reactivity in chemical reactions. b-D-ribofuranose is a five-membered ring sugar with specific hydroxyl groups that can be acetylated. Understanding the stereochemistry and functional groups present in the sugar is crucial for predicting the products of the reaction, as different hydroxyl groups may react differently under the same conditions.
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02:21Reducing Sugars
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