Propyne reacts with excess $HBr$ to form the compound $Z$. The structure of $Z$ is:

  • A
    $CH_2(Br)CH_2CH_2Br$
  • B
    $CH_3CH_2CHBr_2$
  • C
    $CH_3CH(Br)CH_2Br$
  • D
    $CH_3CBr_2CH_3$

Explore More

Similar Questions

The reagent needed for converting $Ph-C \equiv C-Ph$ to trans-stilbene is:

$C_6H_5 - C \equiv C - CH_3 \xrightarrow{HgSO_4, H_2SO_4} A$

$(A)$ $\xrightarrow[dil. H_2SO_4]{HgSO_4} (B)$ $\xrightarrow{LiAlH_4} \underset{\text{racemic mixture}}{(C)}$
$\therefore$ reactant $(A)$ is

Difficult
View Solution

$Mg_2C_3 + H_2O \xrightarrow{X}$ (organic compound).
Compound $X$ is

Ozonolysis of acetylene $(HC \equiv CH)$ gives:

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