Compound $A$ (molecular formula $C_3H_8O$) is treated with acidified potassium dichromate to form a product $B$ (molecular formula $C_3H_6O$). $B$ forms a shining silver mirror on warming with ammoniacal silver nitrate,and $B$ when treated with an aqueous solution of $NH_2NHCONH_2$ and sodium acetate gives a product $C$. Identify the structure of $C$.

  • A
    $CH_3CH_2CH=NNHCONH_2$
  • B
    $CH_3C(CH_3)=NNHCONH_2$
  • C
    $CH_3C(CH_3)=NCONHNH_2$
  • D
    $CH_3CH_2CH=NCONHNH_2$

Explore More

Similar Questions

Which of the following reactions converts the carbonyl group of aldehydes and ketones to a methylene group on treatment with zinc amalgam and concentrated $HCl$?

Wolff-Kishner reduction reduces which of the following groups?

The major product $A$ is:

Consider the following reaction sequence:
$B \xleftarrow{NaBH_4} CH_2=CH-CHO \xrightarrow{H_2/Pt} A$
Identify $A$ and $B$.

The product of the above reaction is

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo