Occasionally in organic synthesis, an ionic product is formed. In these cases, it is often necessary to supply the product mixture with an excess of protons to neutralize the ionic product. This can be accomplished by adding an acid- to a product mixture in a separatory funnel. Acids are aqueous and will therefore form the aqueous layer. Some lab activities in Virtual Chemlab, Organic willrequire you to do this. Using the above details, how would you acid neutralize the reactant below (anion) to form the protonated product. Propose a mechanism. SH Acetylide anion

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Chapter1: Chemical Foundations
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I need to propose a mechanism

Occasionally in organic synthesis, an ionic product is formed. In these cases, it is often necessary to
supply the product mixture with an excess of protons to neutralize the ionic product. This can be
accomplished by adding an acid- to a product mixture in a separatory funnel. Acids are aqueous and
will therefore form the aqueous layer. Some lab activities in Virtual Chemlah Organic willrequire you
to do this.
Using the above details, how would you acid neutralize the reactant below (anion) to form the
protonated product. Propose a mechanism.
SH
Acetylide anion
Transcribed Image Text:Occasionally in organic synthesis, an ionic product is formed. In these cases, it is often necessary to supply the product mixture with an excess of protons to neutralize the ionic product. This can be accomplished by adding an acid- to a product mixture in a separatory funnel. Acids are aqueous and will therefore form the aqueous layer. Some lab activities in Virtual Chemlah Organic willrequire you to do this. Using the above details, how would you acid neutralize the reactant below (anion) to form the protonated product. Propose a mechanism. SH Acetylide anion
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