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.For the resulting hydrocarbon to yi

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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.For the resulting hydrocarbon to yield only one monochloro derivative,all hydrogen atoms in the alkane must be equivalent.$t$-Butyl chloride ($CH_3)_3CCl$ reacts with $Na$/dry ether to form $2,2,3,3$-tetramethylbutane: $(CH_3)_3C-C(CH_3)_3$.In $2,2,3,3$-tetramethylbutane,all $18$ hydrogen atoms are equivalent,so its monochlorination produces only one product.Therefore,$A$ is $t$-butyl chloride.

Reactants	Products
$A$. $C_2H_5Cl$,moist $Ag_2O$	$I$. $CH_3CH_2ONO$
$B$. $C_2H_5Cl$,aqueous ethanolic $AgCN$	$II$. $C_2H_4$
$C$. $C_2H_5Cl$,aqueous ethanolic $AgNO_2$	$III$. $CH_3CH_2OH$
$D$. $C_2H_5Cl$,ethanolic $KOH$	$IV$. $CH_3CH_2NC$

An organic compound $A$ $(C_4H_9Cl)$ on reaction with $Na$/dry ether gives a hydrocarbon which on monochlorination gives only one chloro derivative. What is $A$?

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Which of the following compounds will produce a precipitate with $AgNO_3$?

Match the following:
Reactants Products
$A$. $C_2H_5Cl$,moist $Ag_2O$ $I$. $CH_3CH_2ONO$
$B$. $C_2H_5Cl$,aqueous ethanolic $AgCN$ $II$. $C_2H_4$
$C$. $C_2H_5Cl$,aqueous ethanolic $AgNO_2$ $III$. $CH_3CH_2OH$
$D$. $C_2H_5Cl$,ethanolic $KOH$ $IV$. $CH_3CH_2NC$

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