ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG(LL)
ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG(LL)
4th Edition
ISBN: 9781119659587
Author: Klein
Publisher: WILEY
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Chapter 13, Problem 64IP
Interpretation Introduction

Interpretation: The product of the given reaction to be predicted.

Concept Introduction:

Ring-opening reactions of epoxide:

  • Generally, Epoxides have significant ring strain (high in energy), thus it undergoes reaction in which the ring is opened and alleviates the strain. Ring-opening occurs under conditions involving a strong nucleophile or under acid-catalyzed conditions.
  • The reaction transformation involves two mechanistic step:
    1. I. Nucleophilic attack via SN2 process.
    2. II. Proton transfer.
  • Regiochemistry: if the epoxide is unsymmetrical, the nucleophile attacks at the less hindered position (less substituted).
  • Stereochemistry:  when the attack takes place at the chiral center, inversion of configuration is observed. Only the center being attacked undergoes an inversion of configuration.

To Identify: The product of the given reaction to be identified.

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Use the literature Ka value of the acetic acid, and the data below to answer these questions. Note: You will not use the experimental titration graphs to answer the questions that follow.  Group #1:   Buffer pH = 4.35 Group #2: Buffer pH = 4.70 Group #3: Buffer pH = 5.00 Group #4: Buffer pH = 5.30 Use the Henderson-Hasselbalch equation, the buffer pH provided and the literature pKa value of acetic acid to perform the following: a) calculate the ratios of [acetate]/[acetic acid] for each of the 4 groups buffer solutions above. b) using the calculated ratios, which group solution will provide the best optimal buffer (Hint: what [acetate]/[acetic acid] ratio value is expected for an optimal buffer?) c) explain your choice

Chapter 13 Solutions

ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG(LL)

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