$(1)$ $C{H_3} - \mathop {CH}\limits^ \bullet C{H_3}$
$(2)$ (ચિત્ર.)
$(3)$ $\mathop {C{H_2}}\limits^ \bullet - CH{(C{H_3})_2}$
$(4)$ $\mathop {C{H_2}}\limits^ \bullet - C{H_3}$
$(2)$ (fig.)
$(3)$ $\mathop {C{H_2}}\limits^ \bullet - CH{(C{H_3})_2}$
$(4)$ $\mathop {C{H_2}}\limits^ \bullet - C{H_3}$
The stability of free radicals is mostly affected by the factors like resonance, hyperconjugation and inductive effect. In compound $ (II)$, there is high resonance effect due to which it is highly stable than other three compounds. The effect of hyperconjugation is directly proportional to the number alpha hydrogen. So, compound $I$ has six alpha hydrogen atoms, compound $III $ has one alpha hydrogen atom and compound $IV$ has three alpha hydrogen atoms. Therefore, the order is $II > I > IV > III.$

$(1)\,\,{{(C{{H}_{3}})}_{3}}\bar{\ddot{C}}$
$(2)\,\,{{(C{{H}_{3}})}_{2}}\bar{\ddot{C}}$
$\,(3)\,\,C{{H}_{3}}\bar{\ddot{C}}{{H}_{2}}$
$(4)\,\,{{C}_{6}}{{H}_{5}}\bar{\ddot{C}}{{H}_{2}}$

