Title: Why is a terminal alkyne favored when sodium amide (NaNH2) is used in an elimination reaction with ... Post by: Lola617 on Jan 3, 2019 Why is a terminal alkyne favored when sodium amide (NaNH2) is used in an elimination reaction with 2,3-dichlorohexane?
• The positions of the Cl atoms induce the net formation of the terminal alkyne. • The strong base deprotonates the terminal alkyne and removes it from the equilibrium. • The terminal alkyne is not favored in this reaction. • The terminal alkyne is more stable than the internal alkyne and is naturally the favored product. • The resonance favors the formation of the terminal rather than internal alkyne. Title: Why is a terminal alkyne favored when sodium amide (NaNH2) is used in an elimination reaction with ... Post by: tiffanyswh on Jan 3, 2019 Content hidden
Title: Why is a terminal alkyne favored when sodium amide (NaNH2) is used in an elimination reaction with ... Post by: Lola617 on Jan 3, 2019 Smart ... Thanks!
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