Textbook Question
What product is obtained from the reaction of each of the following alcohols with
a. H2CrO4?
1. 3-pentanol
2. 1-pentanol
3. 2-methyl-2-pentanol
Ch. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing Compounds
Bruice8th EditionOrganic ChemistryISBN: 9780135213711
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Table of contents
- Ch. 1 - Remembering General Chemistry: Electronic Structure and Bonding (Part 1)31
- Ch. 1 - Remembering General Chemistry: Electronic Structure and Bonding (Part 2)65
- 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. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing CompoundsProblem 23
Bruice 8th EditionCh. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing CompoundsProblem 23Chapter 11, Problem 23
What are the major products obtained when the following ether is heated with one equivalent of HI?
Verified step by step guidance1
Step 1: Analyze the structure of the ether provided. The ether consists of an oxygen atom bonded to two alkyl groups: ethyl (CH₃CH₂-) and isopropyl (CH₃CH(CH₃)-).
Step 2: Understand the reaction mechanism. When an ether is heated with one equivalent of HI, the bond between the oxygen and one of the alkyl groups is cleaved. The cleavage occurs via an SN2 mechanism if the alkyl group is primary or secondary, and via an SN1 mechanism if the alkyl group is tertiary.
Step 3: Determine which bond will break. In this case, the ethyl group is primary, and the isopropyl group is secondary. The bond between the oxygen and the ethyl group is more likely to break due to the SN2 mechanism being favored for primary alkyl groups.
Step 4: Predict the products. The cleavage of the ether will result in the formation of two products: ethyl iodide (CH₃CH₂I) and isopropanol (CH₃CH(CH₃)OH). The ethyl group reacts with the iodide ion (I⁻), while the isopropyl group retains the hydroxyl group (OH).
Step 5: Summarize the reaction. Heating the ether with one equivalent of HI results in the major products ethyl iodide and isopropanol, formed through the cleavage of the ether bond.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Ethers and Their Reactions
Ethers are organic compounds characterized by an oxygen atom connected to two alkyl or aryl groups. When heated with strong acids like HI, ethers undergo cleavage, breaking the C-O bond. This reaction typically results in the formation of alcohols and alkyl halides, depending on the structure of the ether and the conditions of the reaction.
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How to predict the products of Ether Cleavage.
Hydroiodic Acid (HI) as a Cleavage Agent
Hydroiodic acid is a strong acid that can protonate ethers, making them more susceptible to nucleophilic attack. In the presence of HI, the ether is cleaved to yield iodide ions and alcohols. The reactivity of HI facilitates the breaking of the ether bond, leading to the formation of the corresponding alkyl iodide and alcohol.
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1:45Cleavage of Phenyl Ethers Concept 1
Mechanism of Ether Cleavage
The mechanism of ether cleavage involves protonation of the ether oxygen, followed by nucleophilic attack by iodide ions. This results in the formation of an alkyl iodide and an alcohol. Understanding this mechanism is crucial for predicting the products of the reaction, as the structure of the ether influences the pathway and the major products formed.
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1:57Cleavage of Phenyl Ethers Example 1
Related Practice
Textbook Question
What alcohol would you treat with phosphorus oxychloride and pyridine to form each of the following alkenes?
a.
b.
Textbook Question
What are the major products obtained when each of the following ethers is heated with one equivalent of HI?
e.
1
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Textbook Question
Explain why methyl propyl ether forms both methyl iodide and propyl iodide when it is heated with excess HI.
1
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Textbook Question
What are the major products obtained when each of the following ethers is heated with one equivalent of HI?
c.
d.
1
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Textbook Question
What product is obtained from the reaction of each of the following alcohols with
c. the regents required for a Swern oxidation?
1. 3-pentanol
2. 1-pentanol
3. 2-methyl-2-pentanol