. Like acid chlorides, acid anhydrides react with alcohols in the presence of pyridine to form esters. For the following reaction: (a) Draw a circle around the nucleophile; (b) Draw a square around the electrophile; (c) Put a star next to the base; (d) Draw the structure of the tetrahedral intermediate in the box below. Then draw a reasonable 3-step arrow pushing mechanism for the reaction. pyridine HO Structure of tetrahedral intermediate Iechanism:

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2. Like acid chlorides, acid anhydrides react with alcohols in the presence of pyridine to form
esters. For the following reaction: (a) Draw a circle around the nucleophile; (b) Draw a square
around the electrophile; (c) Put a star next to the base; (d) Draw the structure of the tetrahedral
intermediate in the box below. Then draw a reasonable 3-step arrow pushing mechanism for
the reaction.
pyridine
+
но
Structure of tetrahedral intermediate
Mechanism:
Transcribed Image Text:2. Like acid chlorides, acid anhydrides react with alcohols in the presence of pyridine to form esters. For the following reaction: (a) Draw a circle around the nucleophile; (b) Draw a square around the electrophile; (c) Put a star next to the base; (d) Draw the structure of the tetrahedral intermediate in the box below. Then draw a reasonable 3-step arrow pushing mechanism for the reaction. pyridine + но Structure of tetrahedral intermediate Mechanism:
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