Urea is not used:

Nitroparaffins on reduction give:

Which of the following is not a nitro derivative?

Which of the following amines is optically active?

(3) ${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{CH}}_2-\stackrel{\stackrel{{\mathrm{CH}}_3}{|}}{\mathrm{N}}-{\mathrm{C}}_2{\mathrm{H}}_5$

The number of $\mathrm{\pi }$-bonds in the formula given below, NC-CH=CH-CN are:

Ketones and $1°$ amines react to form:

Which compound will liberate CO₂ from NaHCO₃ solution?

${\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NO}}_2\stackrel{\mathrm{Fe}/\mathrm{HCl}}{\to }\mathrm{A}\underset{273 \mathrm{K}}{\overset{{\mathrm{NaNO}}_2/\mathrm{HCl}}{\to }}\mathrm{B}\underset{283 \mathrm{K}}{\overset{{\mathrm{H}}_2\mathrm{O}}{\to }}\mathrm{C}$ 'C' is 

Nitrobenzene on reaction with $\mathrm{Conc}. {\mathrm{HNO}}_3/{\mathrm{H}}_2{\mathrm{SO}}_4$ at 80-100 $°$C forms which one of the following products?

Which of the following compounds is most basic here

The melting point is highest for -

Carbylamine test is performed in alcoholic $KOH$ by heating a mixture of 

Hinsberg reagent is 

When acetamide is treated with $NaOBr$, the product formed is

The compound which one reaction with aqueous nitrous acid at low temperature produces an oily nitrosamine is

Which compound is formed when ${\left(C{H}_3\right)}_4{N}^{+}O{H}^{-}$ is heated ?

The reagent that converts nitromethane to methylhydroxylamine is -

An amine that does not give carbylamine reaction is -

Which is most basic?

Which of the following reagent can be used to convert benzenediazonium chloride into benzene

Which of the following reacts with Hinsberg reagent (Benzene sulphonyl chloride) to form a product, soluble in $\mathrm{KOH}$?

 The most reactive towards electrophilic substitution among the following is -

Carbylamine reaction can be given by -

${\mathrm{CH}}_3{\mathrm{NH}}_2+{\mathrm{CHCl}}_3+\mathrm{KOH} \to \mathrm{Nitrogen} \mathrm{containing} \mathrm{compound}+\mathrm{KCl}+{\mathrm{H}}_2\mathrm{O}$. The nitrogen-containing compound is

C₂H₅NH₂ , C₆H₅NHCH₃, (C₂H₅)₂NH and C₆H₅NH₂ 

_{For the above compounds, decreasing order of the pKb values (in gaseous phase) is -}

The increasing order of boiling point of 

 C₂H₅OH, (CH₃)₂NH, C₂H₅NH₂ is-

The increasing sequence of solubility of the following molecules ;C₆H₅NH₂, (C₂H₅)₂NH, C₂H₅NH₂  

in water is -

Arrange the following in increasing order of their basic strength: CH₃NH₂, (CH₃)₂NH, (CH₃)₃N, C₆H₅NH₂, C₆H₅CH₂NH₂

_{$$\begin{gathered} 1. {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}< {\mathrm{CH}}_3{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH} \\ 2. {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\mathrm{CH}}_3{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH} \\ 3. {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH}< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\mathrm{CH}}_3{\mathrm{NH}}_2 \\ 4. {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}<{\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\mathrm{CH}}_3{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH} \end{gathered}$$}

${\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{N}}_2\mathrm{Cl}+{\mathrm{H}}_3{\mathrm{PO}}_2+{\mathrm{H}}_2\mathrm{O}$:

The product from the above reaction would be -

Arrange the following in increasing order of their basic strength: ${\left({\mathrm{CH}}_3\right)}_2\mathrm{NH}, {\mathrm{CH}}_3{\mathrm{NH}}_2, {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}, {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2, {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2$

_{$$\begin{gathered} 1. {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}< {\mathrm{CH}}_3{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH} \\ 2. {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\mathrm{CH}}_3{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH} \\ 3. {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH}< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\mathrm{CH}}_3{\mathrm{NH}}_2 \\ 4. {\left({\mathrm{CH}}_3\right)}_3\mathrm{N}<{\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2< {\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2{\mathrm{NH}}_2 < {\mathrm{CH}}_3{\mathrm{NH}}_2< {\left({\mathrm{CH}}_3\right)}_2\mathrm{NH} \end{gathered}$$}