Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
8th Edition
ISBN: 9781305864504
Author: Brent L. Iverson, Sheila Iverson
Publisher: Cengage Learning
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Chapter 18, Problem 18.39P

(a)

Interpretation Introduction

Interpretation:

Possible mechanism for the given reaction has to be proposed.

Concept Introduction:

Reaction of an ester with ammonia or an amine:

Treatment of an ester with ammonia or a primary or secondary amine gives an amide.

The nucleophilic addition of the ammonia or amine to the carbonyl carbon occurs followed by a proton transfer and a tetrahedral addition intermediate is formed. The intermediate can directly alkoxide and lose a proton to the alkoxide to give products.

Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition, Chapter 18, Problem 18.39P

(b)

Interpretation Introduction

Interpretation:

More acidic has to be identified in the given barbital molecule and the acidity of this molecule has to be accounted.

Concept Introduction:

PKaValue: The pKa value computes the acidity of an acid. This value depends upon the chemical property and identity of the compound.

            pKa= - log Ka

Where,

Ka is the measure of strength of an acid. If the acid is strong means Ka on the order of 1010 and weak means Ka on the order of 1050. Strong acid means pKa value is low value and Weak acid means pKa value is high.

If we know which proton is the more acidic and which proton is the less acidic we can make the determination regarding basicity.

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Chapter 18 Solutions

Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition

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