Organic Chemistry, Binder Ready Version
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
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Chapter 26, Problem 45PP
Interpretation Introduction

Interpretation:

Mechanism for the base-catalyzed transesterification of trimyristin using ethanol 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.  This can occur in presence of either acid or base as catalyst.  The general scheme can be shown as,

Organic Chemistry, Binder Ready Version, Chapter 26, Problem 45PP

Please remember that transesterification using basic condition is done in few steps rather than acidic conditions.

To draw: the mechanism for the base-catalyzed transesterification.

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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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