MCQ
An isocyanide on hydrolysis gives
- AAn amide
- BA carboxylic acid and ammonia
- CA $N-$substituted amide
- ✓A $1^o$- amine and formic acid
✓
Answer
Correct option: D.
A $1^o$- amine and formic acid
d
(d)$R - NC + 2{H_2}O \to RN{H_2} + HCOOH$.
(d)$R - NC + 2{H_2}O \to RN{H_2} + HCOOH$.
Need a full question paper?
Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.
Explore more
Similar questions
Which of the following structures is enantiomeric with the molecule (A) given below:
In which of the following reaction $2^o$ alcohol is obtained as a product ?
→Given below are certain cations. Using inorganic qualitative analysis, arrange them in increasing group number from 0 to $\mathrm{VI}$.
→$A$. $Al^{3+}$ $B$. $Cu^{2+}$ $C$. $Ba^{2+}$ $D$. $Co^{2+}$ $E$. $Mg^{2+}$
Choose the correct answer from the options given below.
The reaction of ethyl methyl ketone with $Cl_2$ excess $OH^-$ gives the following major product
→An example of a disaccharide is:
The electrode potentials for
→$C{u^{2 + }}_{{\text{(aq)}}}\, + \,\,{e^ - }\, \to \,C{u^ + }_{{\text{(aq)}}}$
and $C{u^+}_{{\text{(aq)}}}\, + \,\,{e^ - }\, \to \,C{u }_{{\text{(s)}}}$
are $+0.15\,V$ and $+0.50\,V$ respectively. The value of will be ............ $\mathrm{V}$
Assertion : Nitration of benzoic acid gives $m-$ nitrobenzoic acid.
Reason : Carboxyl group increases the electrondensity at meta-position
→Reason : Carboxyl group increases the electrondensity at meta-position
Four alkali metals $A, B, C $ and $D$ are having respectively standard electrode potential as $ -3.05,-1.66,-0.40$ and $0.80$. Which one will be the most reactive
→$298 \mathrm{~K}$. It could be increased by :
→Product $(C)$ of the reaction is
→