Tre 2.) Given the final product and reagents for each step in the forward synthesis of this cyclohexane-containing internal alkyne, please propose the structures for the synthetic intermediates A-E below.

Organic Chemistry
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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...
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3) Tre 2.) Given the final product and reagents for each step in the forward synthesis of this
nd t cyclohexane-containing internal alkyne, please propose the structures for the synthetic
the cur intermediates A-E below. s
KOC(CH3)3
Br2
KOC(CH3)3
NaNH2
E
CH3I
(2 equiv)
DMSO
CHOH
but-2ayne
N-chlorosucclinimide
Transcribed Image Text:3) Tre 2.) Given the final product and reagents for each step in the forward synthesis of this nd t cyclohexane-containing internal alkyne, please propose the structures for the synthetic the cur intermediates A-E below. s KOC(CH3)3 Br2 KOC(CH3)3 NaNH2 E CH3I (2 equiv) DMSO CHOH but-2ayne N-chlorosucclinimide
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