Draw the possible products of this epoxide ring-opening reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts. 4111 タ 1) NaOH/ H₂O 2) dilute HCI TH L K

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 24.39P: E. J. Coreys 1964 total synthesis of -caryophyllene (essence of cloves) solves a number of problems...
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Draw the possible products of this epoxied ring opening reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts. 

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Aktiv Chemistry
!
app.aktiv.com
Draw the possible products of this epoxide ring-opening
reaction. Use a dash or wedge bond to indicate
stereochemistry of substituents on asymmetric centers, Ignore
any inorganic byproducts.
F1
4/11
14
O
X
1) NaOH / H₂O
2) dilute HCI
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F2
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F3
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F4
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do
%
Canvas LMS
오
F5
Problem 12 of 20
tv ♫♬
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F6
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Transcribed Image Text:← → C esc N k Aktiv Chemistry ! app.aktiv.com Draw the possible products of this epoxide ring-opening reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts. F1 4/11 14 O X 1) NaOH / H₂O 2) dilute HCI -☀ y MCPBA - Yahoo Search Result X F2 # H K NOV C 5 80 JO F3 $ F4 OOO do % Canvas LMS 오 F5 Problem 12 of 20 tv ♫♬ X F6 + Pleas & S F7
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