Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide
Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide
3rd Edition
ISBN: 9781119351610
Author: David Klein
Publisher: Wiley Plus
Question
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Chapter 27, Problem 41PP

(a)

Interpretation Introduction

Interpretation:

Syndiotactic poly (vinyl chloride) segments need to be drawn.

Concept introduction:

If the polymer formed has chiral centers then with the relative configuration of the chiral centers the polymers can be classified as isotactic, Syndiotactic or atactic.  When monosubstituted ethylenes are used as monomer the polymer formed has huge number of chiral centers.  Isotactic means all the chiral center has the same configuration.  Syndiotactic means the chiral centers has alternating configuration.  Atactic means the chiral centers are in random arrangement.

Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide, Chapter 27, Problem 41PP , additional homework tip  1

(b)

Interpretation Introduction

Interpretation:

Isotactic polystyrene segments need to be drawn.

Concept introduction:

If the polymer formed has chiral centers then with the relative configuration of the chiral centers the polymers can be classified as isotactic, Syndiotactic or atactic.  When monosubstituted ethylenes are used as monomer the polymer formed has huge number of chiral centers.  Isotactic means all the chiral center has the same configuration.  Syndiotactic means the chiral centers has alternating configuration.  Atactic means the chiral centers are in random arrangement.

Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide, Chapter 27, Problem 41PP , additional homework tip  2

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Questions 4 and 5
For a titration of 40.00 mL of 0.0500 M oxalic acid H2C2O4 with 0.1000 M KOH, calculate the pH at each of the following volume of KOH used in the titration: 1) before the titration begin;2) 15 mL; 3) 20 mL; 4) 25 mL; 5) 40 mL; 6) 50 mL. Ka1 = 5.90×10^-2, Ka2 = 6.50×10^-5 for oxalic acid.
Predict the major organic product(s), if any, of the following reactions.  Assume all reagents are in excess unless otherwise indicated.
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