Which of the following carbocations is the most stable?

Arrange the following free radicals in order of decreasing stability:
$(A)$ Cyclohexyl-CH2-CH2•
$(B)$ Cyclohexyl-$CH$•-CH3
$(C)$ Cyclohexyl=$CH$-CH2•
(Note: The dot represents the radical center.)

Which of the following is not expected to be an intermediate of the following reaction?

The stability of the following carbanions is in the order of:

The decreasing order of hydride affinity for the following carbocations is:
$A: CH_2=CH-C^+(CH_3)_2$
$B: (C_6H_5)_3C^+$
$C: (CH_3)_3C^+$
$D: (Cyclopropyl)_3C^+$
Choose the correct answer from the options given below:

Arrange the following in decreasing order of stability.
$(i)$ $CH_3^{\bullet}$,$(CH_3)_3C^{\bullet}$,$(CH_3)_2CH^{\bullet}$ and $CH_3CH_2^{\bullet}$
$(ii)$ $CH_3CH_2^{+}$,$(CH_3)_3C^{+}$,$(CH_3)_2CH^{+}$ and $CH_3^{+}$