Ask Experts Questions for FREE Help !
Ask
    harvard896's Avatar
    harvard896 Posts: 1, Reputation: 1
    New Member
     
    #1

    Feb 16, 2014, 07:00 PM
    Halogenation
    Hi,
    I was wondering why only tertiary alcohol undergo halogenation(I know they are more reactive but what is the reason)?


    Thank you!
    ma0641's Avatar
    ma0641 Posts: 15,675, Reputation: 1012
    Uber Member
     
    #2

    Feb 16, 2014, 09:19 PM
    Methyl bromide is produced from CH3OH and HBr >CH3Br and HOH. Primary and secondary alcohols can be brominated.

Not your question? Ask your question View similar questions

 

Question Tools Search this Question
Search this Question:

Advanced Search

Add your answer here.


Check out some similar questions!

Halogenation of acetone [ 1 Answers ]

In my experiment, the concentrations stays the same in the mixture,which was made up of acetone, sulphuric acid and iodone. The mixture was titrated against sodium thiosulphate. Aliquots were withdrawn every 7 minutes. We withdrew six aliquots. The endpoint or the reaction between the iodine...


View more questions Search