Refer to Question. When the compound `(B)` on ozonolysis is followed by oxidation with `H_(2)O_(2)`, the products are `:`

Options

A.
B.
C.
D.

Explanation

To solve the problem, we need to analyze the ozonolysis of compound (B) and the subsequent oxidation with H₂O₂. Here’s a step-by-step breakdown of the solution:

### Step 1: Understand Ozonolysis
Ozonolysis is a reaction where an alkene is cleaved by ozone (O₃) to form carbonyl compounds. This process involves breaking the carbon-carbon double bond and adding oxygen to the resulting fragments.

**Hint:** Remember that ozonolysis typically results in the formation of aldehydes or ketones.

### Step 2: Identify the Structure of Compound (B)
Assuming compound (B) is an alkene, we need to visualize its structure. For this example, let’s consider a simple alkene like 2-butene (CH₃-CH=CH-CH₃).

**Hint:** Draw the structure of the alkene you are considering to visualize the double bond.

### Step 3: Perform Ozonolysis
When 2-butene undergoes ozonolysis, the double bond is broken, and oxygen is added to the fragments. This results in the formation of two carbonyl compounds:

1. Acetone (CH₃-C(=O)-CH₃)
2. Acetaldehyde (CH₃-CH₂-C(=O)-H)

**Hint:** After breaking the double bond, remember to add oxygen to both ends of the broken bond.

### Step 4: Identify the Products
The products of ozonolysis from 2-butene are acetone (a ketone) and acetaldehyde (an aldehyde).

**Hint:** Identify whether the carbonyl compounds formed are aldehydes or ketones, as this will affect the next step.

### Step 5: Oxidation with H₂O₂
Now, we need to consider the oxidation of the products with hydrogen peroxide (H₂O₂).

- **Aldehyde (Acetaldehyde)**: This will be oxidized to a carboxylic acid (acetic acid).
- **Ketone (Acetone)**: Ketones generally do not undergo oxidation with H₂O₂.

Thus, after oxidation, we will have:
1. Acetic acid (from acetaldehyde)
2. Acetone remains unchanged.

**Hint:** Remember that aldehydes are more easily oxidized than ketones.

### Step 6: Final Products
The final products after ozonolysis followed by oxidation with H₂O₂ are acetic acid and acetone.

**Hint:** Summarize the final products clearly to ensure you understand the outcome of the reactions.

### Conclusion
The products obtained from the ozonolysis of compound (B) followed by oxidation with H₂O₂ are acetic acid and acetone.