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5. Diisobutylaluminum hydride (pictured below) reacts with nitrile A to form product B, which no longer contains a nitrile. While we have not yet seen this reaction in this course, you will be able to answer the following questions given the information below. CN 1. н в 2. Hо" A a. What change(s) in the IR spectrum are consistent with the disappearance of A as the reaction progresses? b. The IR spectrum and molecular formula of B are shown below. Use arrows to point out important IR stretches and label each arrow with the type of bond or functional group present. You may find some helpful information on page 7.

5. Diisobutylaluminum hydride (pictured below) reacts with nitrile A to form product B, which no longer contains a nitrile. While we have not yet seen this reaction in this course, you will be able to answer the following questions given the information below. CN 1. н в 2. Hо" A a. What change(s) in the IR spectrum are consistent with the disappearance of A as the reaction progresses? b. The IR spectrum and molecular formula of B are shown below. Use arrows to point out important IR stretches and label each arrow with the type of bond or functional group present. You may find some helpful information on page 7.

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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5. Diisobutylaluminum hydride (pictured below) reacts with nitrile A to form product B, which no longer contains a nitrile. While we have not yet seen this reaction in this course, you will be able to answer the following questions given the information below. Al 1. H CN в 2. Hао A a. What change(s) in the IR spectrum are consistent with the disappearance of A as the reaction progresses? b. The IR spectrum and molecular formula of B are shown below. Use arrows to point out important IR stretches and label each arrow with the type of bond or functional group present. You may find some helpful information on page 7.
Transcribed Image Text:5. Diisobutylaluminum hydride (pictured below) reacts with nitrile A to form product B, which no longer contains a nitrile. While we have not yet seen this reaction in this course, you will be able to answer the following questions given the information below. Al 1. H CN в 2. Hао A a. What change(s) in the IR spectrum are consistent with the disappearance of A as the reaction progresses? b. The IR spectrum and molecular formula of B are shown below. Use arrows to point out important IR stretches and label each arrow with the type of bond or functional group present. You may find some helpful information on page 7.
b. The IR spectrum and molecular formula of B are shown below. Use arrows to point out important IR stretches and label each arrow with the type of bond or functional group present. You may find some helpful information on page 7. 100 3000 VEN Rat c. Propose the structure of compound B.
Transcribed Image Text:b. The IR spectrum and molecular formula of B are shown below. Use arrows to point out important IR stretches and label each arrow with the type of bond or functional group present. You may find some helpful information on page 7. 100 3000 VEN Rat c. Propose the structure of compound B.
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