21.50 Determine the combinations of haloalkane(s) and alkoxide(s) that could be used to synthesize the following ethers through Williamson ether synthesis. (a) (c) (d) (e) (f) H₂CO 21.41 From each pair, select the stronger base. (a) or (b) or (d) (c) or H&C H&C Reactions at the Benzylic Position 21.44 Identify the products of each reaction. (a) (b) H₂ (1 mol) Pt or Cl₂ (excess) light CH3CH₂Br (d) H₂CrO (e) OH K2Cr2O7 H₂SO4
21.50 Determine the combinations of haloalkane(s) and alkoxide(s) that could be used to synthesize the following ethers through Williamson ether synthesis. (a) (c) (d) (e) (f) H₂CO 21.41 From each pair, select the stronger base. (a) or (b) or (d) (c) or H&C H&C Reactions at the Benzylic Position 21.44 Identify the products of each reaction. (a) (b) H₂ (1 mol) Pt or Cl₂ (excess) light CH3CH₂Br (d) H₂CrO (e) OH K2Cr2O7 H₂SO4
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
Chapter24: Catalytic Carbon-carbon Bond Formation
Section: Chapter Questions
Problem 24.26P: The compound eutypine is an antibacterial agent isolated from the fungus Eutypa lata. This fungus...
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Transcribed Image Text:21.50 Determine the combinations of haloalkane(s) and alkoxide(s) that could be used to
synthesize the following ethers through Williamson ether synthesis.
(a)
(c)
(d)
(e)
(f)
H₂CO

Transcribed Image Text:21.41 From each pair, select the stronger base.
(a)
or
(b)
or
(d)
(c)
or
H&C
H&C
Reactions at the Benzylic Position
21.44 Identify the products of each reaction.
(a)
(b)
H₂ (1 mol)
Pt
or
Cl₂ (excess)
light
CH3CH₂Br
(d)
H₂CrO
(e)
OH
K2Cr2O7
H₂SO4
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