EscContent54°FClear*Aktiv Chemistryapp.101edu.coDraw the major product of the substitution reaction shownbelow. Ignore any inorganic byproducts.F1CH3CO2HEdit SN1 ProductX OSN2/SN1 Reactions Fl: XF2F3BrOHxF4âG Which alkyl bromide X G whats aF5Question 13 of 224)6F6Please seleVF7

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Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts.

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

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.52P: Alcohols are important for organic synthesis, especially in situations involving alkenes. The...

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Aktiv Chemistry
app.101edu.co
Draw the major product of the substitution reaction shown
below. Ignore any inorganic byproducts.
F1
CH3CO2H
Edit SN1 Product
X OSN2/SN1 Reactions Fl: X
F2
F3
Br
OH
x
F4
â
G Which alkyl bromide X G whats a
F5
Question 13 of 22
4)
6
F6
Please sele
V
F7

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Alcohols are important for organic synthesis, especially in situations involving alkenes. The alcohol might be the desired product, or the OH group might be transformed into another functional group via halogenation, oxidation, or perhaps conversion to a sulfonic ester derivative. Formation of an alcohol from an alkene is particularly powerful because conditions can be chosen to produce either the Markovnikov or non-Markovnikov product from an unsymmetrical alkene. Using your reaction roadmap as a guide, show how to convert 4-methyl-1-pentene into 5-methylhexanenitrile. You must use 4-methyl-1-pentene and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.
[Review Topics] [References] HO pyridine 1. SOCIl, + sO2 + H. Aqueous acetone H3C H20 H3C HBr 2. Br H OH optically active racemic f = SN1 Nucleophilic substitution g = SN2 Nucleophilic substitution a = Proton transfer d = E1 Elimination b = Lewis acid/base e = E2 Elimination c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2.