English
Karnataka Board PUCPUC Science 2nd PUC Class 12

Write the mechanism of hydration of ethene to yield ethanol.

Advertisements
Advertisements

Question

Write the mechanism of hydration of ethene to yield ethanol.

Short Answer
Very Short Answer
Advertisements

Solution 1

Step 1: Protonation of the alkene to form a carbocation by the electrophilic attack of H3O+.

\[\ce{H2O + H+ -> H3O+}\]

Step 2: Nucleophilic attack of water on carbocation.

Step 3: Deprotonation to form an alcohol.

shaalaa.com

Solution 2

The acid-catalysed hydration of ethene may be represented as:

The mechanism followed by the above reaction may be depicted as:

Step 1: Generation of carbocation: Protonation of ethene yields a carbocation as,

Step 2: Nucleophilic attack of water on carbocation: The carbocation polarises the lone pair electrons of O of water, and hydration takes place.

Step 3: Formation of product, regeneration of the proton:

shaalaa.com
  Is there an error in this question or solution?
Chapter 7: Alcohols, Phenols and Ethers - Exercises [Page 222]

APPEARS IN

NCERT Chemistry Part 1 and 2 [English] Class 12
Chapter 7 Alcohols, Phenols and Ethers
Exercises | Q 7.11 | Page 222

RELATED QUESTIONS

Name the reagents used in the following reactions:


Name the reagents used in the following reactions:


Write the structures of the main products when acetone (CH3 − CO − CH3) reacts with the following reagents :

CH3MgBr and then H3O+


Show how will you synthesize 1-phenylethanol from a suitable alkene.


How is the following conversion carried out?

\[\ce{Propene -> Propan-2-ol}\]


Name the reagent used in the following reaction:

Butan-2-one to butan-2-ol.


Write the structures of A, B and C in the following reactions :

\[{CH}_3 CI \to^{KCN} A \to^{LiAIH} B \to^{{HNO}_2}_{273K} C\]

Primary alcohols are prepared by the reduction of carboxylic acids. Though lithium aluminium hydride is a strong reducing agent, it is not used in the reaction. This is so because:


Aldehydes are reduced to the corresponding alcohols by the addition of hydrogen in the presence of catalysts to form ____________.


Monochlorination of toluene in sunlight followed by hydrolysis by aq. \[\ce{NaOH}\] yields.


Alkenes convert into alcohols by ____________.


Acetone reacts with Grignard reagent to form:


Select the acid(s) which cannot be prepared by Grignard reagent.


The best reagent to convert pent 3 – en 2 – 01 into pent 3 – in – 2 – one is


Glycerol is used in the manufacture


An aldehyde isomeric with allyl alcohol gives phenyl hydrazone. Pick out a ketone that too gives a phenyl hydrazone containing the same percentage of nitrogen.


For distinction between \[\ce{CH3CHO}\] and \[\ce{C6H5CHO}\] the reagent used is ______.


How are the following conversions carried out?

\[\ce{Methyl magnesium bromide ->2-Methylpropan-2-ol}\]


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×