Given below are two statements :

Statement I : On the basis of inductive effect, the order of stability of alkyl carbanions is $\mathrm{CH}_3{ }^{-}>\mathrm{CH}_3-\mathrm{CH}_2{ }^{-}>\left(\mathrm{CH}_3\right)_2 \mathrm{CH}^{-}>\left(\mathrm{CH}_3\right)_3 \mathrm{C}^{-}$.

Statement II : Allyl and benzyl carbanions are more stabilised by inductive effect and not by resonance effect.

In the light of the above statements, choose the correct answer from the options given below :

For the following Friedel Craft's alkylation reaction, which of the statements are correct?

A. Major product is n-propyl benzene.

B. iso-propyl carbocation intermediate is also generated.

C. Multiple substitution is inevitable.

D. Introducing electron-donating substituent on benzene will not produce any alkyl benzene.

Choose the correct answer from the options given below :

$$ \text {Benzyl isocyanide can be obtained from } $$

Choose the correct answer from the options given below :

Consider compounds $\mathrm{A}, \mathrm{B}$ and C with following structural formulae

$$ \begin{aligned} & \mathrm{A}=\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{OH} \\ & \mathrm{~B}=\mathrm{CH}_2=\mathrm{CH}-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}_3 \\ & \mathrm{C}=\mathrm{HO}-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}(\mathrm{OH})-\mathrm{CH}_3 \end{aligned} $$

For the conversion of B from A , reagent (D) required is $\_\_\_\_$ and structural formula of product $(\mathrm{E})$ obtained when C undergoes same reaction using excess reagent (D) is $\_\_\_\_$ .