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Draw the major product of this reaction. Ignore inorganic byproducts and the alkoxide side product. or N H 1. excess LIAIH4 2. H₂O

Draw the major product of this reaction. Ignore inorganic byproducts and the alkoxide side product. or N H 1. excess LIAIH4 2. H₂O

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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**Instruction:** Draw the major product of the reaction. Ignore inorganic byproducts and the alkoxide side product. **Reaction Details:** 1. **Starting Compound:** A cyclic amide structure is provided, specifically, a caprolactam. The molecule consists of a 6-membered ring with an amide linkage (C=O connected to NH). 2. **Reagents:** - Step 1: Excess LiAlH₄ (Lithium aluminum hydride) - Step 2: H₂O (Water) **Reaction Pathway:** LiAlH₄ is a strong reducing agent typically used to reduce amides to amines. When a cyclic lactam like caprolactam is treated with LiAlH₄, it is expected to reduce the amide group to a secondary amine without breaking the ring structure. **Outcome:** The reaction should convert the amide group (C=O) to a methylene (CH₂) linked to nitrogen, resulting in a ring with a secondary amine. **Drawing:** A placeholder is provided indicating where the drawing of the product should go.
Transcribed Image Text:**Instruction:** Draw the major product of the reaction. Ignore inorganic byproducts and the alkoxide side product. **Reaction Details:** 1. **Starting Compound:** A cyclic amide structure is provided, specifically, a caprolactam. The molecule consists of a 6-membered ring with an amide linkage (C=O connected to NH). 2. **Reagents:** - Step 1: Excess LiAlH₄ (Lithium aluminum hydride) - Step 2: H₂O (Water) **Reaction Pathway:** LiAlH₄ is a strong reducing agent typically used to reduce amides to amines. When a cyclic lactam like caprolactam is treated with LiAlH₄, it is expected to reduce the amide group to a secondary amine without breaking the ring structure. **Outcome:** The reaction should convert the amide group (C=O) to a methylene (CH₂) linked to nitrogen, resulting in a ring with a secondary amine. **Drawing:** A placeholder is provided indicating where the drawing of the product should go.
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