I know the answer is D but I do not understand fully. Please explain. Thank you very much!

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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I know the answer is D but I do not understand fully. Please explain. Thank you very much!

The image shows a chemistry problem:

**Question 6:** 
"Select the possible reactant(s) that would give the product shown of the following reaction."

The reaction involves:

1. Use of ozone (O₃) as the first reagent.
2. Use of dimethyl sulfide (Me₂S) as the second reagent.

**Product Structure:**
The product is a linear diketone with carbonyl groups at each end.

**Potential Reactants:**

1. Compound 1: A bicyclic structure composed of two five-membered rings sharing a double bond.
2. Compound 2: A cyclic structure with two six-membered rings and a 3-carbon side chain with a double bond.
3. Compound 3: A polycyclic aromatic hydrocarbon with a methyl group attached.

**Multiple Choice Options:**
- A. 1 only
- B. 2 only
- C. 3 only
- D. 1 and 2
- E. 1 and 3
- F. 2 and 3

This problem requires selecting the reactant(s) that, upon ozonolysis followed by reduction with Me₂S, would yield the given diketone product.
Transcribed Image Text:The image shows a chemistry problem: **Question 6:** "Select the possible reactant(s) that would give the product shown of the following reaction." The reaction involves: 1. Use of ozone (O₃) as the first reagent. 2. Use of dimethyl sulfide (Me₂S) as the second reagent. **Product Structure:** The product is a linear diketone with carbonyl groups at each end. **Potential Reactants:** 1. Compound 1: A bicyclic structure composed of two five-membered rings sharing a double bond. 2. Compound 2: A cyclic structure with two six-membered rings and a 3-carbon side chain with a double bond. 3. Compound 3: A polycyclic aromatic hydrocarbon with a methyl group attached. **Multiple Choice Options:** - A. 1 only - B. 2 only - C. 3 only - D. 1 and 2 - E. 1 and 3 - F. 2 and 3 This problem requires selecting the reactant(s) that, upon ozonolysis followed by reduction with Me₂S, would yield the given diketone product.
Expert Solution
Step 1

Alkenes can be converted into carbonyl compounds on reaction with ozonide followed by cleavage with dimethyl sulfide.

In order to write the products of ozonolysis, simply the break the double bond and attach oxygen atoms to the double bonded carbon atoms.

 

 

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