In the Synthesis of Methyl trans-cinnamte via Fischer Esterification experiment, the following reaction is performed. Draw a detailed arrow pushing mechanism for this reaction? E22A.1 PREPARATION OF METHYL trans-CINNAMATE:A COMPONENT OF STRAWBERRY AROMAOHCC=COHH2SO4H+ CH3OHAtrans-cinnamic acidmethanolHC=COCH3H+ H₂Omethyl trans-cinnamate

It is the esterification of a carboxylic acid by heating with an alcohol in the presence of a strong…

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In the Synthesis of Methyl trans-cinnamte via Fischer Esterification experiment, the following reaction is performed. Draw a detailed arrow pushing mechanism for this reaction?

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

Chapter29: Organic Polymer Chemistry

Section: Chapter Questions

Problem 29.17P: Polycarbonates (Section 29.5C) are also formed by using a nucleophilic aromatic substitution route...

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

In the Synthesis of Methyl trans-cinnamte via Fischer Esterification experiment, the following reaction is performed. Draw a detailed arrow pushing mechanism for this reaction?

E22A.1 PREPARATION OF METHYL trans-CINNAMATE:
A COMPONENT OF STRAWBERRY AROMA
O
H
CC=C
OH
H2SO4
H
+ CH3OH
A
trans-cinnamic acid
methanol
H
C=C
OCH3
H
+ H₂O
methyl trans-cinnamate

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