Explain the acidic dehydration of alcohols with an example.

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) Acidic dehydration of alcohols involves the removal of a water molecule from an alcohol in the presence of an acid catalyst to form an alkene.
General Reaction:
$CH_3-CH_2-OH \xrightarrow[\Delta, 443 \ K]{Conc. \ H_2SO_4} CH_2=CH_2 + H_2O$
Mechanism and Explanation:
$1$. In this reaction,the $-OH$ group is removed from the $\alpha$-carbon,and a hydrogen atom is removed from the $\beta$-carbon.
$2$. This results in the formation of a $\pi$-bond between the $\alpha$ and $\beta$ carbons.
$3$. Because a hydrogen atom is eliminated from the $\beta$-position,this process is also known as a $\beta$-elimination reaction.
$4$. Common dehydrating agents used include concentrated $H_2SO_4$,$H_3PO_4$,or anhydrous $Al_2O_3$ at high temperatures.

Explore More

Similar Questions

$CH \equiv CH$ $\xrightarrow{Hg^{2+}/H_2SO_4} B$ $\xrightarrow{CH_3MgX/H_2O} C$ $\xrightarrow{[O]} D$. What is the final product $D$?

Difficult
View Solution

Find the major product for the following reaction.

Identify the correct trend of acidic strength for the given alcohols.

Find out the major product from the following reaction.

Which of the following alcohols has the highest solubility in water?

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