Free Radical Stability Homework: Find the Optimal Temp

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    Radical Stability
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The discussion centers on determining the optimal temperature for free radical stability, with options presented as 1°C and 3°C. Participants debate the significance of stabilizing factors, particularly the mesomeric effect, which influences radical stability. The conversation highlights the preference for universal terminology, such as tertiary and primary carbons, over numerical designations. It is noted that radical stability trends align with carbocation stability, emphasizing that resonance structures should be considered for greater clarity. Ultimately, understanding the interplay of these factors is crucial for accurately determining radical stability.
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Homework Statement

Homework Equations

The Attempt at a Solution


option 1: 1 degree C
option 2: 1 degree C
option 3: 3 degree C
option 4: 1 degree C

SO the answer should be option 3?
 
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Is that the only stabilizing factor involved here?
Any polar effect involved?
PS- always thought saying tertiary or secondary carbon was a more universal naming system
 
Suraj M said:
Is that the only stabilizing factor involved here?
Any polar effect involved?
PS- always thought saying tertiary or secondary carbon was a more universal naming system
Why would there be a polar effect? Carbon and hydrogen have very similar electronegativities.
Yeah tertiary and primary are the universal terms, somehow this book doesn't refer to them as tertiary and primary carbons but as 1 degree, 2 degree and 3 degree carbons.
 
By polar effect, I am referring to mesmeric effect in this case
 
Suraj M said:
By polar effect, I am referring to mesmeric effect in this case
If the mesomeric effect is considered, then option 3 and 4 are ruled out. But I don't understand why I can't just see which carbon is tertiary and say that's the most stable.
 
Mesmeric effect ALWAYS dominates here
 
Decide between 1 and 2 then
 
I suggest thinking about what types of resonance give the greatest stability. Also consider drawing out resonance structures. Radical stability trends closely resemble carbocation trends (tertiary > secondary > primary). Think about where aromaticity fits into this trend.
 

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