The most common method for the synthesis of unsymmetrical ethers is the Williamson synthesis, a reaction (SN2) of an alkoxide ion with an alkyl halide. Two pathways are possible, but often one is preferred. Construct the preferred pathway for the synthesis of 2-propoxypropane from propene, with propene-derived alkyl halide and alkoxide intermediates, by dragging the appropriate intermediates and reagents into their bins. Not every given reagent or intermediate will be used HBr но Br CH2CI2 Step 1 Product BзН6 H2O2 Reagent 1 Br Na Но propene Reagent 2 Reagent 3 Nat о. H20 Step 2 Product Step 3 Product H2SO4 HBr ROOR + - NaBr NaH 2-propoxypropane

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter9: Nucleophilic Substitution And Β-elimination
Section: Chapter Questions
Problem 9.48P: The Williamson ether synthesis involves treatment of a haloalkane with a metal alkoxide. Following...
icon
Related questions
Question
100%
The most common method for the synthesis of unsymmetrical ethers is the Williamson synthesis, a reaction
(SN2) of an alkoxide ion with an alkyl halide. Two pathways are possible, but often one is preferred. Construct
the preferred pathway for the synthesis of 2-propoxypropane from propene, with propene-derived alkyl halide
and alkoxide intermediates, by dragging the appropriate intermediates and reagents into their bins. Not every
given reagent or intermediate will be used
HBr
но
Br
CH2CI2
Step 1
Product
BзН6
H2O2
Reagent 1
Br
Na
Но
propene
Reagent 2
Reagent 3
Nat
о.
H20
Step 2
Product
Step 3
Product
H2SO4
HBr
ROOR
+
- NaBr
NaH
2-propoxypropane
Transcribed Image Text:The most common method for the synthesis of unsymmetrical ethers is the Williamson synthesis, a reaction (SN2) of an alkoxide ion with an alkyl halide. Two pathways are possible, but often one is preferred. Construct the preferred pathway for the synthesis of 2-propoxypropane from propene, with propene-derived alkyl halide and alkoxide intermediates, by dragging the appropriate intermediates and reagents into their bins. Not every given reagent or intermediate will be used HBr но Br CH2CI2 Step 1 Product BзН6 H2O2 Reagent 1 Br Na Но propene Reagent 2 Reagent 3 Nat о. H20 Step 2 Product Step 3 Product H2SO4 HBr ROOR + - NaBr NaH 2-propoxypropane
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning
Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning