Textbook Question
Explain why the acid-catalyzed condensation is a poor method for the synthesis of an unsymmetrical ether such as ethyl methyl ether, CH3CH2-O-CH3.
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Ch.11 - Reactions of Alcohols
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 11, Problem 24a
Contrast the mechanisms of the two preceding reactions, the dehydration and condensation of ethanol.
Verified step by step guidance1
Understand the two reactions: Dehydration of ethanol involves the removal of a water molecule to form ethene, while condensation of ethanol involves the combination of two ethanol molecules to form a larger molecule (e.g., diethyl ether) with the elimination of water.
For the dehydration mechanism: Recognize that it typically occurs under acidic conditions (e.g., H₂SO₄ or H₃PO₄) and heat. The first step involves protonation of the hydroxyl group (-OH) of ethanol, making it a better leaving group.
In the dehydration mechanism, after protonation, the -OH group leaves as water, forming a carbocation intermediate. This is followed by the elimination of a proton (H⁺) from a neighboring carbon, resulting in the formation of a double bond (ethene).
For the condensation mechanism: This reaction also occurs under acidic conditions but at lower temperatures. The hydroxyl group of one ethanol molecule is protonated, making it a better leaving group. A second ethanol molecule then attacks the carbocation formed, leading to the formation of an ether bond.
In the condensation mechanism, after the nucleophilic attack by the second ethanol molecule, a proton is lost to regenerate the acid catalyst, and the final product (e.g., diethyl ether) is formed along with water as a byproduct.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Dehydration Reaction
A dehydration reaction involves the removal of a water molecule from a reactant, typically resulting in the formation of a double bond or a new functional group. In the case of ethanol, dehydration can lead to the formation of ethylene (ethene) when heated in the presence of an acid catalyst. This process is crucial in organic synthesis as it helps in the formation of alkenes from alcohols.
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01:23
General Reaction of Dehydration with POCl3
Condensation Reaction
A condensation reaction is a chemical process where two molecules combine to form a larger molecule, accompanied by the loss of a small molecule, often water. In the context of ethanol, condensation can occur when two ethanol molecules react to form diethyl ether, releasing water in the process. This type of reaction is fundamental in forming larger organic compounds and polymers.
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Reaction Mechanisms
Reaction mechanisms describe the step-by-step sequence of elementary reactions by which overall chemical change occurs. Understanding the mechanisms of dehydration and condensation reactions of ethanol involves analyzing the intermediates and transition states formed during the reactions. This knowledge is essential for predicting the products and understanding the conditions required for each reaction.
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Related Practice
Textbook Question
Predict the products of the sulfuric acid-catalyzed dehydration of the following alcohols. When more than one product is expected, label the major and minor products.
(d) 1-isopropylcyclohexanol
(e) 2-methylcyclohexanol
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Textbook Question
Some alcohols undergo rearrangement or other unwanted side reactions when they dehydrate in acid. Alcohols may be dehydrated under mildly basic conditions using phosphorus oxy-chloride (POCl3) in pyridine. The alcohol reacts with phosphorus oxychloride much like it reacts with tosyl chloride (Section 11-5), displacing a chloride ion from phosphorus to give an alkyl dichlorophosphate ester. The dichlorophosphate group is an outstanding leaving group. Pyridine reacts as a base with the dichlorophosphate ester to give an E2 elimination. Propose a mechanism for the dehydration of cyclohexanol by POCl3 in pyridine.
Textbook Question
Propose a mechanism for each reaction.
(a)
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Textbook Question
Give the structures of the products you would expect when each alcohol reacts with (1) HCl, ZnCl2; (2) HBr; (3) PBr3; (4) P/I2; and (5) SOCl2.
(a) butan-1-ol
(b) 2-methylbutan-2-ol
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Textbook Question
Propose a mechanism for each reaction.
(c)
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