$A$ solution of optically active $1$-phenylethanol racemizes in acidified aqueous medium. It is due to

  • A
    enolization
  • B
    carbonium ion formation
  • C
    carbanion formation
  • D
    reversible oxidation-reduction

Explore More

Similar Questions

Order of reactivity of alcohols towards sodium metal is

What is the final product $(IV)$ in the following reaction sequence? $CH_3-CH(OH)-CH_3$ $\xrightarrow{PBr_3} I$ $\xrightarrow{Mg/ether} II$ $\xrightarrow{\text{Ethylene oxide}} III$ $\xrightarrow{H_2O} IV$

Write the main product of the given reactions:
$1$. $(CH_3)_2CHCHBrCH_3 \xrightarrow[ethanol]{KOH, \Delta }$
$2$. $(CH_3)_2CHCH(OH)CH_3 \xrightarrow{H_2SO_4, \Delta }$

Difficult
View Solution

What is the product '$A$' in the following reaction?
(Image of an epoxide ring fused to a cyclopentane ring with an exocyclic double bond,reacting with $H_3O^{\oplus}$ to form $A$.)

Which is the best reagent to convert isopropyl alcohol to isopropyl bromide?
$CH_3-CH(OH)-CH_3 \xrightarrow{?} CH_3-CH(Br)-CH_3$

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