Organic Chemistry Study Guide and Solutions
Organic Chemistry Study Guide and Solutions
6th Edition
ISBN: 9781936221868
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
bartleby

Videos

Question
Book Icon
Chapter 4, Problem 4.69AP
Interpretation Introduction

(a)

Interpretation:

The stability of 1-butene and 2-methylpropene is to be compared.

Concept introduction:

Gibbs free energy is the useful work obtained from the system. It is the difference between the enthalpy and the product of entropy and absolute temperature. It is always negative. Therefore, more negative the gibbs free energy more stable the compound.

Interpretation Introduction

(b)

Interpretation:

The hydration reaction between 1-butene and 2-methylpropene is to be compared.

Concept introduction:

In hydration reaction, water molecules attack on a compound and it is an exothermic reaction. The molecule has standard activation energy to get hydrated. Lower the activation energy faster will be the hydration of that molecule.

Interpretation Introduction

(c)

Interpretation:

The free-energy-diagrams representing the hydration reaction of alkenes, 2-methylpropene and 1-butene on same scale with the relative free energies of both starting materials and rate-determining transition states are to be drawn.

Concept introduction:

Gibbs free energy is the useful work obtained from the system. The free energy diagram represents the gibbs free energy of reactants and products. The lower the gibbs free energy more stable the compound.

Interpretation Introduction

(d)

Interpretation:

The difference in the standard free energies of the transition states for the hydration reactions of 1-butene and 2-methylpropene using the mechanism is to be stated. The molecule which has lower transition state energy is to be stated. The reason fot the stable transition state is to be stated.

Concept introduction:

Gibbs free energy is the useful work obtained from the system. In hydration, the compound reacts with water to release energy. Hydration reaction has activation energy. Higher the activation energy, lower will be the rate of reaction. A reactant has to undergo transition state, transition state has highest energy than reactant and product. More stable the carbocation formed on hydration, lesser will be the transition state energy.

Blurred answer
Students have asked these similar questions
Kumada Coupling: 1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a mechanism and give two reasons why you would NOT get the desired product. Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene. Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?
Wintergreen from Aspirin: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? 2. Write the mechanism of the esterification reaction you did. 3. What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional group change. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?
Synthesis of ZybanⓇ: 1. Write a mechanism for the bromination of m-chloropropiophenone. Br₂ CH2Cl2 Cl Br 2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks). 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
The Laws of Thermodynamics, Entropy, and Gibbs Free Energy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=8N1BxHgsoOw;License: Standard YouTube License, CC-BY