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$A$ carbanion acts as a:

Which of the following carbocations is the most stable?

The geometry of the reaction intermediate in an $S_N1$ reaction is:

What is the decreasing order of stability for the following carbocations?
$(i)$ $CH_3-CH^{+}-CH_3$
$(ii)$ $CH_3-CH^{+}-OCH_3$
$(iii)$ $CH_3-CH^{+}-COCH_3$

State whether the following statements are True or False:
$(i)$ $CH_3-CH_2^+$ is more stable than $CH_3^+$
$(ii)$ $CH_3-CH_2^+$ is less stable than $CH_3^+$
$(iii)$ $(CH_3)_3C^+$ is less stable than $CH_3^+$
$(iv)$ $(CH_3)_3C^+$ is more stable than $CH_3^+$

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