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

Expert verified

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.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Write a rate equation for each reaction, given the indicated mechanism.

a.

b.

Draw an energy diagram for a two-step reaction, ABC, where the relative energy of these compounds is C<A<B, and the conversion of BCis rate-determining.

The conversion of (CH3)3Clto (CH3)2C=CH2can occur by either a one-step or a two-step mechanism, as shown in Equations [1] and [2].

a. What rate equation would be observed for the mechanism in Equation [1]?

b. What rate equation would be observed for the mechanism in Equation [2]?

c. What is the order of each rate equation (i.e., first, second, and so forth)?

d. How can these rate equations be used to show which mechanism is the right one for this reaction?

e. Assume Equation [1] represents an endothermic reaction and draw an energy diagram for the reaction. Label the axes, reactants, products, Ea, and H°. Draw the structure for the transition state.

f. Assume Equation [2] represents an endothermic reaction and that the product of the rate-determining step is higher in energy than the reactants or products. Draw an energy diagram for this two-step reaction. Label the axes, reactants and products for each step, and the Eaand H°for each step. Label H°overall. Draw the structure for both transition states.

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.

Indicate which factors affect the rate of a reaction.

  1. G°
  2. H°
  3. Ea
  4. Temperature
  5. concentration
  6. width="28">Keq
  7. k
  8. Catalysts
See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free