What is the correct order of stability for the following carbocations?

Given below are two statements:
Statement $I$: $(CH_3)_3C^{+}$ is more stable than $CH_3^{+}$ as nine hyperconjugation interactions are possible in $(CH_3)_3C^{+}$.
Statement $II$: $CH_3^{+}$ is less stable than $(CH_3)_3C^{+}$ as only three hyperconjugation interactions are possible in $CH_3^{+}$.
In the light of the above statements,choose the correct answer from the options given below.

Number of carbocations from the following that are not stabilized by hyperconjugation is $...........$ .

Intermediates formed in the reactions $P$ and $Q$ are:
$P: CH_3-CH=CH_2 \xrightarrow{HCl}$
$Q: CH_3-CH=CH_2 \xrightarrow[\text{Peroxide}]{HCl}$

Which of the following has an unstable enol form?

Match the intermediates given in Column $-I$ with their probable structure in Column $-II$.

Column $-I$	Column $-II$
$A$. Free radical	$1$. Trigonal planar
$B$. Carbocation	$2$. Pyramidal
$C$. Carbanion	$3$. Linear