Organic Chemistry
Organic Chemistry
2nd Edition
ISBN: 9781118452288
Author: David R. Klein
Publisher: WILEY
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Chapter 26.4, Problem 3LTS
Interpretation Introduction

Interpretation:

Mechanism for transesterification of trilaurin using ethanol in presence of acid catalyst need to be drawn.

Concept introduction:

Transesterification is a process in which the alcohol group present in the carboxylate of triglyceride is exchanged by another organic alcohol group.  The general scheme can be shown as,

Organic Chemistry, Chapter 26.4, Problem 3LTS

The steps involved in transesterification is,

  • Protonation
  • Nucleophilic attack
  • Deprotonation
  • Protonation
  • Loss of leaving group
  • Deprotonation

To draw: the mechanism of transesterification of trilaurin using ethanol in presence of acid catalyst.

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6. Consider the following exothermic reaction below. 2Cu2+(aq) +41 (aq)2Cul(s) + 12(aq) a. If Cul is added, there will be a shift left/shift right/no shift (circle one). b. If Cu2+ is added, there will be a shift left/shift right/no shift (circle one). c. If a solution of AgNO3 is added, there will be a shift left/shift right/no shift (circle one). d. If the solvent hexane (C6H14) is added, there will be a shift left/shift right/no shift (circle one). Hint: one of the reaction species is more soluble in hexane than in water. e. If the reaction is cooled, there will be a shift left/shift right/no shift (circle one). f. Which of the changes above will change the equilibrium constant, K?
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