An organic compound A (C_4H_9Cl) on reaction | vedclass

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(A) The reaction of an alkyl halide with $Na$ in dry ether is the $Wurtz$ reaction,which produces a symmetric alkane. $A$ is $t$-butyl chloride,$(CH_3

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$t$-butyl chloride

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(A) The reaction of an alkyl halide with $Na$ in dry ether is the $Wurtz$ reaction,which produces a symmetric alkane. $A$ is $t$-butyl chloride,$(CH_3)_3C-Cl$. Reaction: $2 (CH_3)_3C-Cl + 2 Na \xrightarrow{	ext{ether}} (CH_3)_3C-C(CH_3)_3 + 2 NaCl$. The product is $2,2,3,3$-tetramethylbutane. In $2,2,3,3$-tetramethylbutane,all $18$ hydrogen atoms are equivalent because they are all primary hydrogens attached to methyl groups bonded to quaternary carbons. Thus,monochlorination of this hydrocarbon yields only one chloro derivative.

An organic compound $A$ $(C_4H_9Cl)$ on reaction with $Na$ in diethyl ether gives a hydrocarbon,which on monochlorination gives only one chloro derivative. $A$ is:

Similar Questions

Given below are two statements:
Statement $I$ : $C_2H_5OH$ and $AgCN$ both can generate nucleophile.
Statement $II$ : $KCN$ and $AgCN$ both will generate nitrile nucleophile with all reaction conditions.
Choose the most appropriate option :

The major product is:

The correct reactivity order of the following compounds towards alkaline hydrolysis is:-
$I. \ p-CH_3O-C_6H_4-CH_2Cl$
$II. \ C_6H_5-CH_2Cl$
$III. \ p-CH_3-C_6H_4-CH_2Cl$
$IV. \ m-CH_3-C_6H_4-CH_2Cl$

The optically inactive compound from the following is

An alkyl bromide reacts with sodium ethoxide and ethanol to give only one alkene. Hydrogenation of this alkene yields $2-$methylbutane. What is the alkyl halide?

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