71.
In the following sequence of reactions
\[\underset{A}{\mathop{C{{H}_{3}}C{{H}_{2}}I}}\,\xrightarrow[\text{ether}]{Mg}B\xrightarrow{HCHO}C\xrightarrow{{{H}_{2}}O}D\]
the compound $$D$$ is
On hydrolysis both gives different compounds.
\[\underset{\text{Ethylene dichlorid}e}{\mathop{C{{H}_{2}}Cl-C{{H}_{2}}Cl}}\,\xrightarrow{aq.\,KOH}\] \[\underset{\text{Glycol}}{\mathop{C{{H}_{2}}OH-C{{H}_{2}}OH}}\,\]
75.
Which of the following haloalkanes is most reactive?
The alkyl halides are highly reactive, the order of reactivity is Iodide > Bromide > Chloride ( nature of the halogen atom ).
Tertiary > Secondary > Primary.
Thus, 2-bromopropane is the most reactive.
76.
The reaction, \[C{{H}_{2}}=CH-C{{H}_{3}}+HBr\to \] \[C{{H}_{3}}\overset{\begin{smallmatrix}
Br\,\, \\
|\,\,\,\,
\end{smallmatrix}}{\mathop{-CH-}}\,C{{H}_{3}}\] is an example of
78.
An alkyl chloride produces a single alkene on reaction with sodium ethoxide and ethanol. The alkene further undergoes hydrogenation to yield 2-methylbutane. Identify the alkyl chloride amongst the following compounds.
A
$$ClC{H_2}CH\left( {C{H_3}} \right)C{H_2}C{H_3}$$
B
$$ClC{H_2}C{H_2}C{H_2}C{H_3}$$
C
$$ClC{H_2}CH\left( {C{H_3}} \right)C{H_2}C{H_3}$$
D
$$C{H_3}C\left( {Cl} \right)\left( {C{H_3}} \right)C{H_2}C{H_3}$$
79.
Halogen acids react with alcohols to form alkyl halides. The reaction follows a nucleophilic substitution mechanism. What will be the major product of the following reaction?
\[C{{H}_{3}}\overset{\begin{smallmatrix}
\,\,C{{H}_{3}} \\
|\,\,\,\,
\end{smallmatrix}}{\mathop{-CH-}}\,\underset{\begin{smallmatrix}
|\,\,\,\,\,\,\,\,\,\, \\
OH\,\,\,\,\,\,\,\,
\end{smallmatrix}}{\mathop{CH-}}\,C{{H}_{3}}+HCl\to \]
A
\[\underset{\begin{smallmatrix}
| \\
\,\,\,C{{H}_{3}}
\end{smallmatrix}}{\mathop{C{{H}_{3}}CH-}}\,\underset{\begin{smallmatrix}
|\,\,\,\,\,\,\,\,\,\,\, \\
Cl\,\,\,\,\,\,\,\,\,\,\,
\end{smallmatrix}}{\mathop{CH-}}\,C{{H}_{3}}\]
B
\[\underset{\begin{smallmatrix}
| \\
Cl
\end{smallmatrix}}{\mathop{C{{H}_{3}}CH-}}\,\underset{\begin{smallmatrix}
|\,\,\,\,\,\,\,\,\,\, \\
C{{H}_{3}}\,\,\,\,\,\,
\end{smallmatrix}}{\mathop{CH-}}\,C{{H}_{3}}\]
C
\[C{{H}_{3}}\underset{\begin{smallmatrix}
| \\
Cl
\end{smallmatrix}}{\overset{\begin{smallmatrix}
\,\,\,\,\,C{{H}_{3}} \\
|
\end{smallmatrix}}{\mathop{-C-}}}\,C{{H}_{2}}C{{H}_{3}}\]
D
\[C{{H}_{3}}C{{H}_{2}}C{{H}_{2}}C{{H}_{2}}C{{H}_{2}}Cl\]
4 - nitrobenzyl chloride is likely to react by the $${S_N}2$$ mechanism as the strongly electron-withdrawing nitro group would destabilize the carbocation intermediate of the $${S_N}1$$ mechanism, a benzylic chloride that disfavours the $${S_N}1$$ mechanism.