Alkenes react with water in the presence of acid to form alcohols. Identify the steps involved in the mechanism of the reaction from the following :
a) Nucleophilic addition of hydroxide ion to alkene
b) Protonation of alkene by electrophilic attack of $H_3O^{+}$
c) Electrophilic attack of $H_2O$ on carbanion
d) Nucleophilic attack of $H_2O$ on carbocation
e) Loss of $^{\ominus}OH$ to form an alcohol
f) Loss of $H^{\oplus}$ to form an alcohol

  • A
    $a, c, e$
  • B
    $b, c, e$
  • C
    $b, d, f$
  • D
    $a, c, f$

Explore More

Similar Questions

Which process converts olefins into paraffins?

$2-$methylbut$-2-$ene $\xrightarrow[\text{(ii) } Zn / H_2 O]{\text{(i) } O_3}$ products here are . . . . . . .

What is the product formed when ethene reacts with acidic $KMnO_4$ solution?

Reaction of $HBr$ with propene in the presence of peroxide gives

Ozonolysis of an organic compound gives formaldehyde as one of the products. This indicates the presence of:

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