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What is the major organic product(s) of the following reaction? Draw the product on your file and name the compound below. If you cannot name it, describe it.

What is the major organic product(s) of the following reaction? Draw the product on your file and name the compound below. If you cannot name it, describe it.

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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**Question:** What is the major organic product(s) of the following reaction? Draw the product on your file and name the compound below. If you cannot name it, describe it. **Reaction:** The starting material is a molecule containing a carbonyl group (C=O) with a chlorine atom attached to the carbon adjacent to the carbonyl carbon. Reagents: 1. Lithium aluminium tri-tert-butoxy hydride (LiAlH[OC(CH₃)₃]₃) 2. Water (H₂O) **Explanation:** Lithium aluminium tri-tert-butoxy hydride is a reducing agent that is selective for the reduction of acyl chlorides to aldehydes. The reaction proceeds with lithium aluminium tri-tert-butoxy hydride converting the acyl chloride to an aldehyde. The subsequent step involves hydrolysis with water.
Transcribed Image Text:**Question:** What is the major organic product(s) of the following reaction? Draw the product on your file and name the compound below. If you cannot name it, describe it. **Reaction:** The starting material is a molecule containing a carbonyl group (C=O) with a chlorine atom attached to the carbon adjacent to the carbonyl carbon. Reagents: 1. Lithium aluminium tri-tert-butoxy hydride (LiAlH[OC(CH₃)₃]₃) 2. Water (H₂O) **Explanation:** Lithium aluminium tri-tert-butoxy hydride is a reducing agent that is selective for the reduction of acyl chlorides to aldehydes. The reaction proceeds with lithium aluminium tri-tert-butoxy hydride converting the acyl chloride to an aldehyde. The subsequent step involves hydrolysis with water.
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