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The most stable radical among the follow...

The most stable radical among the following is :

A

`{:(CH_(2)-CH_(2)^(*)),(|),(NO_(2)):}`

B

`{:(CH_(2)-CH_(2)^(*)),(|),(COO^(-)):}`

C

`{:(C_(2)-CH_(2)^(*)),(|),(CH_(3)):}`

D

`{:(CH_(2)-CH_(2)^(*)),(|),(O^(-)):}`

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AI Generated Solution

The correct Answer is:
To determine the most stable radical among the given options, we need to analyze the nature of the substituents attached to each radical and their effects on stability. ### Step-by-Step Solution: 1. **Identify the radicals**: We have four radicals to consider. Let's denote them as: - Radical A - Radical B - Radical C - Radical D 2. **Understand radical stability**: Free radicals are species with an unpaired electron. Their stability is influenced by the presence of substituents that can either donate or withdraw electron density. Electron-donating groups (EDGs) can stabilize radicals, while electron-withdrawing groups (EWGs) can destabilize them. 3. **Analyze the substituents**: - **Radical A**: Contains an electron-withdrawing group (e.g., NO2 or COO-). - **Radical B**: Contains an electron-withdrawing group (e.g., NO2 or COO-). - **Radical C**: Contains an electron-donating group (e.g., CH3). - **Radical D**: Contains an electron-donating group (e.g., O-CH3). 4. **Evaluate the effects of substituents**: - For **Radicals A and B**: The presence of electron-withdrawing groups (NO2 or COO-) will destabilize the radicals due to the -I effect, which pulls electron density away from the radical center. - For **Radical C (CH3)**: The methyl group (CH3) is an electron-donating group, but it is not as effective as other groups in stabilizing radicals. - For **Radical D (O-CH3)**: The methoxy group (O-CH3) has an oxygen atom that can donate electron density more effectively than a carbon atom. The oxygen has a lone pair of electrons that can help stabilize the radical. 5. **Conclusion**: Among the radicals analyzed, Radical D (O-CH3) is the most stable due to the strong electron-donating ability of the oxygen atom, which stabilizes the unpaired electron in the radical. ### Final Answer: The most stable radical among the given options is **Radical D (O-CH3)**. ---
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