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Compound A has the formula C„H and is known not to contain any triple 10 16 bonds. When treated with excess hydrogen and a platinum catalyst, Compound A is converted to compound B with the formula CH,„: Compound B can be identified as 2,6-dimethyloctane. Ozonolysis of compound A followed by treatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of acetone (CH COCH,), and compound C with the formula C,H,0,.

Compound A has the formula C„H and is known not to contain any triple 10 16 bonds. When treated with excess hydrogen and a platinum catalyst, Compound A is converted to compound B with the formula CH,„: Compound B can be identified as 2,6-dimethyloctane. Ozonolysis of compound A followed by treatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of acetone (CH COCH,), and compound C with the formula C,H,0,.

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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[VII] Instructions: Answer the following: (Refer to the photo below)

1. What is the index of hydrogen deficiency of Compound A?

2. How many rings does Compound A contain?

3. How many double bonds does Compound A contain?

Compound A has the formula C„H and is known not to contain any triple 10 16 bonds. When treated with excess hydrogen and a platinum catalyst, Compound A is converted to compound B with the formula CH,„: Compound B can be identified as 2,6-dimethyloctane. Ozonolysis of compound A followed by treatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of acetone (CH COCH,), and compound C with the formula C,H,0,.
Transcribed Image Text:Compound A has the formula C„H and is known not to contain any triple 10 16 bonds. When treated with excess hydrogen and a platinum catalyst, Compound A is converted to compound B with the formula CH,„: Compound B can be identified as 2,6-dimethyloctane. Ozonolysis of compound A followed by treatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of acetone (CH COCH,), and compound C with the formula C,H,0,.
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