Home
Class 12
CHEMISTRY
Formation of methyl tertiary butyl ether...

Formation of methyl tertiary butyl ether by the reaction of sodium tertiary butoxide and methyl bromide involves

A

elimination reaction

B

electrophilic addition reaction

C

nucleophilic addition reaction

D

nucleophilic substitution reaction

Text Solution

Verified by Experts

The correct Answer is:
B
Promotional Banner

Topper's Solved these Questions

  • ALCOHOLS, PHENOLS AND ETHERS

    AAKASH SERIES|Exercise EXAMPLES|41 Videos
  • ALCOHOLS, PHENOLS AND ETHERS

    AAKASH SERIES|Exercise EXERCISE - 2.1.1|9 Videos
  • ALCOHOLS, PHENOLS AND ETHERS

    AAKASH SERIES|Exercise ETHERS(Objective exercise-2)|9 Videos
  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise Exercise 3.2|41 Videos

Similar Questions

Explore conceptually related problems

Methyl bromide to propanone

Ester formation involves the reaction of

From which of the following, tertiary butyl alcohol is obtained by the action of methyl magnesium iodide ?

When methyl iodide reacts with sodium ethoxide it forms

Friedel-Crafts reaction of bromobenzene with methyl chloride gives

What product is expected when tertiary butyl bromide is reacted with sodium ethoxide? Why that product is not formed and how that product can be obtained?

Preparation of ethers by acid dehydration of secondary or tertiary alcohols is not a suitable method. Give reason.

Preparation of ethers by acid dehydration of secondary or tertiary alcohols is not a suitable method. Give reason.

The oxidation of aryl methyl or cyclo alkyl methyl by the treatment with chromyl chloride to an aldehyde via the formation of esters is known as Etard reaction. The oxidation stops at aldehyde stage because the product of the reaction is acylal, R - CH(OCOCH_3)_2 which is resistance to oxidation with this reagent. The acylal on hydrolysis gives aldehyde. What is the product obtained when ethyl benzene is subjected to Etard reaction ?

The oxidation of aryl methyl or cyclo alkyl methyl by the treatment with chromyl chloride to an aldehyde via the formation of esters is known as Etard reaction. The oxidation stops at aldehyde stage because the product of the reaction is acylal, R - CH(OCOCH_3)_2 which is resistance to oxidation with this reagent. The acylal on hydrolysis gives aldehyde. Which of the other reactions will produce benzaldehyde ?