Among the aromatic isomers with the molecular formula $C_8H_8O$,one isomer $X$ gives the iodoform test,while another isomer $Y$ gives the Benedict's test. What are the structures of $X$ and $Y$ respectively?

  • A
    $X = \text{Acetophenone}, Y = \text{Phenylacetaldehyde}$
  • B
    $X = \text{Acetophenone}, Y = \text{Benzaldehyde}$
  • C
    $X = o-\text{Methylbenzaldehyde}, Y = \text{Phenylacetaldehyde}$
  • D
    $X = p-\text{Methylbenzaldehyde}, Y = \text{Acetophenone}$

Explore More

Similar Questions

Arrange the following compounds in the increasing order of their equilibrium constants for the formation of a hydrate:
$(I)$ $6$-amino-$1$-tetralone
$(II)$ $7$-amino-$1$-tetralone
$(III)$ $1$-tetralone
$(IV)$ $6$-nitro-$1$-tetralone

Which of the following does not give an aldol reaction with dil. $NaOH$?

The product $B$ is formed by the reaction of cyclohexanone with hydroxylamine $(NH_2OH)$ to form an oxime $(A)$,followed by a Beckmann rearrangement using polyphosphoric acid $(PPA)$. Identify the product $B$.

Difficult
View Solution

Which of the following gives aldol condensation reaction?

Which of the following gives a positive iodoform test?

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