Free radical stability increases with the number of alkyl substituents due to hyperconjugation and inductive effects. Tertiary radicals like (CH\textsubscript{3})\textsubscript{3}C• are most stable, followed by secondary (CH\textsubscript{3}–CH–CH\textsubscript{3}•), primary (CH\textsubscript{3}•), and least stable are vinylic radicals like CH\textsubscript{2}=CH•.