Chemical Reactions of Haloalkanes

What is the order of reactivity of following compounds towards  $S_N{}^1$ substitutions reaction.
(i) 

(ii) 

(iii) 

What is the order of reactivity of following compounds towards  ${\mathrm{S}}_{\mathrm{N}}1$ substitution reaction.

Which one of the following two substances undergoes ${\mathrm{S}}_{\mathrm{N}}1$ reaction faster?

(i)    or   (ii) 

(CH₃)₃CMgCl on reaction with D₂O produces –

An S_N2 reaction at an asymmetric carbon of a compound always gives:

A solution of (+) -2-chloro-2-phenylethane in toluene racemises slowly in the presence of small amount of  $SbC{l}_5$ , due to the formation of –

A solution of (+) -2-chloro-1-phenylethane in toluene racemises slowly in the presence of small amount of  ${\mathrm{SbCl}}_5$, due to the formation of:

n–propyl bromide on treatment with ethanolic potassium hydroxide produces

The major product of the following reaction is

The product of following reaction is –

${\text{C}}_2{\text{H}}_5{\text{O}}^{-}+\text{C}{\text{H}}_3\text{C}{\text{H}}_2\text{I}\to$

In the reaction, ${\mathrm{CH}}_3\mathrm{Br} \stackrel{\mathrm{KCN}}{⟶} \mathrm{A} \stackrel{{\mathrm{H}}^{+}}{\to } \mathrm{B} \stackrel{{\mathrm{LiAlH}}_4}{⟶} \mathrm{C}$

The product C is.

In the following question a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.

Assertion: $\mathrm{KCN}$ reacts with methyl chloride to give methyl isocyanide.
Reason: ${\mathrm{CN}}^{–}$ is an ambident nucleophile.

Saytzeff's rule states that _____ product is the major product in dehydrohalogenation of an alkyl halide.

Which of the following best describes Saytzeff's rule?

Match the alkyl halide reacting with reagent given in Column $\mathrm{I}$ with their respective substituted product given in  Column $\mathrm{II}$ and choose the correct option from the codes given below: 

Which of the given options shows the correct product of the reaction, $\mathrm{MeCl}+\mathrm{RNa}⟶?$