Textbook Question
Show a complete mechanism for this reaction.
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Ch. 18 - Ketones and Aldehydes
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
Chapter 18, Problem 68b
One of these reacts with dilute aqueous acid and the other does not. Give a mechanism for the one that reacts, and show why this mechanism does not work for the other one.
(b) 
Verified step by step guidance1
Identify the functional groups present in both compounds. Look for groups that are known to react with dilute aqueous acid, such as esters, amides, or epoxides.
Determine the reactivity of each functional group with dilute aqueous acid. For example, esters can undergo hydrolysis in the presence of acid, while amides are generally more resistant.
For the compound that reacts, propose a mechanism. If it is an ester, the mechanism involves protonation of the carbonyl oxygen, followed by nucleophilic attack by water, leading to the formation of a tetrahedral intermediate.
Explain why the mechanism does not work for the other compound. If the other compound is an amide, discuss the resonance stabilization of the amide bond, which makes it less susceptible to acid-catalyzed hydrolysis.
Illustrate the complete mechanism for the reacting compound, showing each step with curved arrows to indicate electron movement, and highlight the key differences in structure or stability that prevent the reaction in the non-reacting compound.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Acid-Base Reactions
Acid-base reactions involve the transfer of protons (H+) between reactants. In organic chemistry, understanding how different functional groups interact with acids is crucial. For example, alcohols can react with acids to form alkyl halides through protonation, while other groups, like alkenes, may not undergo the same reaction due to their structural characteristics.
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The Lewis definition of acids and bases.
Reaction Mechanisms
A reaction mechanism outlines the step-by-step process by which reactants transform into products. It includes details about bond breaking and forming, intermediates, and transition states. For the compound that reacts with dilute aqueous acid, the mechanism may involve protonation followed by nucleophilic attack, while the non-reacting compound may lack a suitable site for protonation or nucleophilic attack.
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Functional Group Reactivity
Different functional groups exhibit varying reactivities based on their electronic and steric properties. For instance, alcohols are generally more reactive towards acids than alkenes due to their ability to form stable carbocations. Understanding the specific functional groups present in the compounds in question is essential to predict their behavior in acid reactions.
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Related Practice
Textbook Question
Within each set of structures, indicate which will react fastest, and which slowest, toward nucleophilic addition in basic conditions.
(c)
2
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Textbook Question
The nucleosides that make up DNA have heterocyclic rings linked to deoxyribose by an aminoacetal functional group. Point out the aminoacetal linkages in deoxycytidine and deoxyadenosine.
2
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Textbook Question
Show a complete mechanism for this equilibrium established in diethyl ether with HCl gas as catalyst.
Textbook Question
One of these reacts with dilute aqueous acid and the other does not. Give a mechanism for the one that reacts, and show why this mechanism does not work for the other one.
(a)
1
views
Textbook Question
Within each set of structures, indicate which will react fastest, and which slowest, toward nucleophilic addition in basic conditions.
(b)
2
views