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Esterification is the reaction of a carboxylic acid (RCOOH) with an alcohol (R'OH) to form an ester (RCOOR') with a loss of water. Equation [1] is an example of an intermolecular esterification reaction. Equation [2] is an example of an intramolecular esterification reaction; that is, the carboxylic acid and alcohol are contained in the same starting material, forming a cyclic ester as the product. The equilibrium constants for both reactions are given. Explain why Keqis different for these two apparently similar reactions.

[1]

[2]

Short Answer

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Answer

Entropy does not play a role in reaction[1] as the number of molecules present in the starting material and the products are similar. The entropy increases in reaction[2] as the small molecule of starting material lead to product formation.

Step by step solution

01

Step-by-Step SolutionStep 1: Esterification

Esterification reactions are reactions where an ester is created when alcohol and carboxylic acid are combined. Acid anhydrides can also combine with alcohol to generate an ester.

02

Equilibrium constant Keq

The equilibrium constant connects the quantity of starting material with the product at equilibrium.The equilibrium acts to the right if the equilibrium constant Keq is greater than one. It acts to the left if the equilibrium constant is less than one.

03

Difference in the equilibrium constant for the given reactions

Entropy does not have a role in reaction[1] as the number of molecules of reactants and products is similar. In reaction [2], the single-molecule of starting material leads to form two products, so the entropy increases.

This leads ∆G° to becoming more favorable, thereby leading to an increase in Keq.

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Most popular questions from this chapter

As we will learn in Section 15.12, many antioxidants—compounds that prevent unwanted radical oxidation reactions from occurring—are phenols, compounds that contain an OH group bonded directly to a benzene ring.

  1. Explain why homolysis of the O-H bond in phenol requires considerably less energy than homolysis of the O-H bond in ethanol (362 kJ/mol vs 438 kJ/mol).
  2. Why is the C-O bond in phenol shorter than C-O bond in ethanol?

Question: Draw an energy diagram for a reaction in which the products are higher in energy than the starting materials and Eais large. Clearly label all of the following on the diagram: the axes, the starting materials, the products, the transition state, ∆H°,and Ea.

Given each value, determine whether the starting material or the product is favored at equilibrium.

a.Keq=0.5

b.∆G°=-100kJ/mol

c.∆H°=8.0kJ/mol

d. Keq=16

e.∆G°=-2.0kJ/mol

f.∆H°=200kJ/mol

g.∆S°=8J/(K.mol)

h.∆S°=-8J/(K.mol)

PGF2α (Section 4.15) is synthesized in cells using a cyclooxygenase enzyme that catalyzesa multistep radical pathway. Two steps in the pathway are depicted in the accompanying equations.

(a) Draw in curved arrows to illustrate how C is converted to D in Step [1].

(b) Identify Y, the product of Step [2], using the curved arrows that are drawn on compound D.

Consider the following energy diagram for the conversion of A→G.

a. Which points on the graph correspond to transition states?

b. Which points on the graph correspond to reactive intermediates?

c. How many steps are present in the reaction mechanism?

d. Label each step of the mechanism as endothermic or exothermic.

e. Label the overall reaction as endothermic or exothermic.

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