Primary alcohols can also dehydrate to alkenes. Unlike secondary and tertiary alcohols, the dehydration reaction occurs under an E2 elimination instead of an El mechanism, due to the instability of the primary carbocation that would be formed. H, SO, Consider the reaction: CH,CH,CH,CH,OH product Draw the expected dehydration product of 1 equiv. of a primary alcohol. Select Draw Rings More Erase

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
Section16.SE: Something Extra
Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...
icon
Related questions
Question
Primary alcohols can also dehydrate to alkenes. Unlike secondary and tertiary alcohols, the dehydration reaction occurs under
an E2 elimination instead of an El mechanism, due to the instability of the primary carbocation that would be formed.
H, SO,
Consider the reaction: CH, CH,CH,CH,OH
product
Draw the expected dehydration product of 1 equiv. of a primary alcohol.
Select
Draw
Rings
More
Erase
Transcribed Image Text:Primary alcohols can also dehydrate to alkenes. Unlike secondary and tertiary alcohols, the dehydration reaction occurs under an E2 elimination instead of an El mechanism, due to the instability of the primary carbocation that would be formed. H, SO, Consider the reaction: CH, CH,CH,CH,OH product Draw the expected dehydration product of 1 equiv. of a primary alcohol. Select Draw Rings More Erase
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 1 images

Blurred answer
Knowledge Booster
Types of Polymers on the Basis of Physical Properties
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning