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Draw the mechanism for formation of the two addition products.
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Ch. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing Compounds
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. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing CompoundsProblema 36b
Bruice 8th EditionCh. 10 - Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing CompoundsProblema 36bCapitolo 10, Problema 36b
The existence of the NIH shift was established by determining the major product obtained from rearrangement of the following arene oxide, in which a hydrogen has been replaced by a deuterium.
b. What would be the major product if the carbocation forms phenol by losing H+ or D+, rather than by going through the NIH shift?
Guida verificata passo dopo passo1
Step 1: Analyze the structure of the arene oxide provided in the image. The molecule contains a benzene ring with an epoxide group attached, where one hydrogen is replaced by deuterium (D). Additionally, there is a methyl group (-CH3) attached to the benzene ring.
Step 2: Understand the reaction conditions. The presence of HB+ indicates acidic conditions, which can lead to the opening of the epoxide ring. This process typically involves protonation of the oxygen atom in the epoxide, making it more electrophilic and susceptible to nucleophilic attack.
Step 3: Consider the mechanism of ring opening. Protonation of the epoxide oxygen leads to the formation of a carbocation intermediate. The carbocation can undergo rearrangement via the NIH shift, where the deuterium (D) migrates to the adjacent carbon, or it can directly lose H+ or D+ to form phenol.
Step 4: If the carbocation loses H+ or D+ without undergoing the NIH shift, the major product will be phenol. The loss of H+ or D+ will result in the formation of a hydroxyl group (-OH) on the benzene ring at the position where the epoxide was originally attached.
Step 5: Predict the major product. If the carbocation loses H+, the phenol product will retain the deuterium (D) at its original position. If the carbocation loses D+, the phenol product will have hydrogen (H) at the position where deuterium was originally located. The major product depends on which proton (H+ or D+) is preferentially lost during the reaction.
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NIH Shift
The NIH shift refers to a specific rearrangement mechanism in organic chemistry where a hydrogen atom is replaced by a deuterium atom during the transformation of an arene oxide to a phenolic compound. This process involves the migration of a hydrogen atom to a neighboring carbon atom, resulting in a new carbocation intermediate. Understanding this shift is crucial for predicting the products of reactions involving arene oxides.
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03:43
Alkyl Shift
Carbocation Stability
Carbocation stability is a key concept in organic chemistry that describes the relative stability of positively charged carbon species. Factors influencing stability include the degree of substitution (primary, secondary, tertiary), resonance effects, and inductive effects from nearby atoms or groups. A more stable carbocation is more likely to form and dictate the pathway of the reaction, impacting the final product.
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05:58Determining Carbocation Stability
Deprotonation Mechanism
Deprotonation is the process of removing a proton (H+ or D+) from a molecule, which can lead to the formation of a stable product such as phenol. In the context of the question, understanding how a carbocation can lose a proton directly to form phenol, rather than undergoing a rearrangement like the NIH shift, is essential for predicting the major product of the reaction. This mechanism highlights the importance of reaction pathways in organic synthesis.
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04:32General Mechanism
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a. What would be the major product if the NIH shift occurs? (Hint: A C—H bond is easier to break than a C—D bond.)
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