Tag: chemistry

Questions Related to chemistry

Reaction at ${ 0-5 }^{ 0 }C$ between aniline, ${ NaNO } { 2 }$ and HCl is known as___________

  1. Suphonation of benzene

  2. Acylation of aniline

  3. Alkylation of aniline

  4. Diazotisation


Correct Option: D
Explanation:

This is the diazotization reaction.


The reaction goes as follows :
$PhNH _{2} + NaNO _{2} + HCl \rightarrow PhN _{2}^{+} Cl^{-}$

The benzendiazonium salt thus formed acts as a synthetic intermediate and can be used to synthesize a wide variety of substituted benzene compounds.

For example,
$PhN _{2}^{+} Cl^{-} + CuCN \rightarrow PhCN$ (cyanobenzene)
$PhN _{2}^{+} Cl^{-} + CuI (KI) \rightarrow PhI$ (iodobenzene)

Option D is correct.

Aniline when treated with $NaNO { 2 }$ and $HCl$ at $0- { 5 }^{ 0 }C$ gives ___________ as a product.

  1. chloroaniline

  2. benzene diazonium chloride

  3. chlorobenzene

  4. dichlorobenzene


Correct Option: B
Explanation:

Aniline reacts with sodium nitrite and HCl in cold condition to form benzene diazonium chloride.
$\underset {aniline} {{ C } _{ 6 }{ H } _{ 5 }{ NH } _{ 2 }}\xrightarrow [ { NaNO } _{ 2 } ]{ HCl } \underset {benzene diazonium chloride} {[C _6H _5-N _2^+Cl^-]}$

Which of the following amines will form stable diazonium salt at 273-283 K? 

  1. $\displaystyle { C } _{ 2 }{ H } _{ 5 }{ NH } _{ 2 }$

  2. $\displaystyle { C } _{ 6 }{ H } _{ 5 }{ NH } _{ 2 }$

  3. $\displaystyle { C } _{ 6 }{ H } _{ 5 }{ CH } _{ 2 }{ NH } _{ 2 }$

  4. $\displaystyle { C } _{ 6 }{ H } _{ 5 }{ N\left( { CH } _{ 3 } \right) } _{ 2 }$


Correct Option: B

Diazonium salts are used at a very lower temperature because:

  1. they are poisonous at room temperature

  2. they are highly unstable at room temperature

  3. they are highly volatile at room temperature

  4. none of these


Correct Option: B
Explanation:

Diazonium salt is used at very low temperature because of the fact that at the higher temperature they are unstable, as at higher temperature $N _2$ can leave out.

Diazonium salts are used:

  1. after storing for a few days after preparation

  2. immediately after its preparation

  3. after storing for $2-3$ hours

  4. difficult to prepare commercially


Correct Option: B
Explanation:

Diazonium salts are light sensitive and break down under near UV or violet light.This is why it is used immedietly after being prepared so that it does not loses its properties.

What makes diazonium ion one of the best leaving group of organic chemistry? 

  1. Half filled electronic configuration of nitrogen atom

  2. High electronegativity of nitrogen atom

  3. Very high stability of dinitrogen molecule in the atmosphere

  4. Weaker $C-N$ bond


Correct Option: C
Explanation:

Diazonium ion is one of best leaving group of organic chemistry because of very high stability of dinitrogen molecule in the atmosphere.

What is the molarity of 0.2 N Na2 CO3 solution ?
  1. 0.1M

  2. 0M

  3. 0.4M

  4. 0.2M


Correct Option: A

Diazomethane was photolysed to generate singlet carbine which was treated with cis-2-butene. The main product(s) of the reaction is/are:

  1. cis-1, 2-dimethylcyclopropane

  2. trans-1, 2-dimethylcyclopropane

  3. mixture of $(A)$ and $(B)$

  4. Ethylcyclopropane


Correct Option: A
Explanation:

Solution:- (A) cis-$1,2$-dimethylcyclopropane

$\underset{\text{Diazomethane}}{C{H} _{2}-\overset{+}{N}={N}^{-}} \xrightarrow[-N \equiv N]{h \nu} \underset{\text{Singlet carbene} \left( \text{Methylene} \right)}{:C{H} _{2}}$
The addition of methylene would yield trans-$1,2$-dimethylcyclopropane from trans-$2$-butene and cis-$1,2$-dimethylcyclopropane from cis-$2$-butene.

Which of the following diazonium salt is relatively stable of $0-5^\circ C$- :

  1. $CH _{3}CH _2N\equiv N\left. \right } ^\oplus Cl^{-} $

  2. $CH _{3}-C(CH _{3}) _{2}-N\equiv N\left. \right } ^\oplus Cl^{-} $

  3. $CH _{3}-N\equiv N\left. \right } ^\oplus Cl^{-} $

  4. $(CH _{3}) _{3}C-N\equiv N\left. \right } ^\oplus Cl^{-} $


Correct Option: C
Explanation:

The diazonium salt  $CH _{3}-N\equiv N\left.  \right } ^\oplus Cl^{-}$ obtained by treatment of methylamine with nitrous acid is relatively stable at $0-5^\circ C$.

Which of the following diazonium salt is relatively stable at $\displaystyle 0-5^{\circ}$C?

  1. $\displaystyle CH _{3}-N\equiv N \left. \right }^{\oplus }Cl^{-}$

  2. $\displaystyle CH _{3}C\left ( CH _{3} \right )-N\equiv N \left. \right }^{\oplus }Cl^{-}$

  3. $\displaystyle C _{6}H _{5}-N\equiv N \left. \right }^{\oplus }Cl^{-}$

  4. $\displaystyle \left ( CH _{3} \right ) _{3}C-N\equiv N \left. \right }^{\oplus }Cl^{-}$


Correct Option: C
Explanation:

Diazonium salts obtained from aliphatic primary amines are unstable. Those obtained from aromatic primary amines are relatively stable.
Benzene diazonium chloride $(\displaystyle C _{6}H _{5}-N\equiv N \left.  \right }^{\oplus }Cl^{-})$ is obtained from aromatic primary amine. Hence, it is relatively stable.