Chemistry: Principles and Practice
Chemistry: Principles and Practice
3rd Edition
ISBN: 9780534420123
Author: Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher: Cengage Learning
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Chapter 19, Problem 19.35QE

(a)

Interpretation Introduction

Interpretation:

The complex, which has three isomers, two of which are enantiomers has to be given from the given set of options.

  (1) [Co(NH3)3Cl3](2) [Co(en)2Br2]+(3) [Cr(H2O)2Cl2Br2](4) [Pt(NH3)3SCN]+(5) [Cr(C2O4)3]3

(b)

Interpretation Introduction

Interpretation:

Linkage isomers having complex has to be given from the given set of options.

  (1) [Co(NH3)3Cl3](2) [Co(en)2Br2]+(3) [Cr(H2O)2Cl2Br2](4) [Pt(NH3)3SCN]+(5) [Cr(C2O4)3]3

(c)

Interpretation Introduction

Interpretation:

The complex, which does not show optically active isomers, has to be given from the given set of options.

  (1) [Co(NH3)3Cl3](2) [Co(en)2Br2]+(3) [Cr(H2O)2Cl2Br2](4) [Pt(NH3)3SCN]+(5) [Cr(C2O4)3]3

(d)

Interpretation Introduction

Interpretation:

The complex that has the greatest number of possible isomers has to be identified and those structures are showed.

  (1) [Co(NH3)3Cl3](2) [Co(en)2Br2]+(3) [Cr(H2O)2Cl2Br2](4) [Pt(NH3)3SCN]+(5) [Cr(C2O4)3]3

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Students have asked these similar questions
What are the IUPAC Names of all the compounds in the picture?
1) a) Give the dominant Intermolecular Force (IMF) in a sample of each of the following compounds. Please show your work. (8) SF2, CH,OH, C₂H₂ b) Based on your answers given above, list the compounds in order of their Boiling Point from low to high. (8)
19.78 Write the products of the following sequences of reactions. Refer to your reaction road- maps to see how the combined reactions allow you to "navigate" between the different functional groups. Note that you will need your old Chapters 6-11 and Chapters 15-18 roadmaps along with your new Chapter 19 roadmap for these. (a) 1. BHS 2. H₂O₂ 3. H₂CrO4 4. SOCI₂ (b) 1. Cl₂/hv 2. KOLBU 3. H₂O, catalytic H₂SO4 4. H₂CrO4 Reaction Roadmap An alkene 5. EtOH 6.0.5 Equiv. NaOEt/EtOH 7. Mild H₂O An alkane 1.0 2. (CH3)₂S 3. H₂CrO (d) (c) 4. Excess EtOH, catalytic H₂SO OH 4. Mild H₂O* 5.0.5 Equiv. NaOEt/EtOH An alkene 6. Mild H₂O* A carboxylic acid 7. Mild H₂O* 1. SOC₁₂ 2. EtOH 3.0.5 Equiv. NaOEt/E:OH 5.1.0 Equiv. NaOEt 6. NH₂ (e) 1. 0.5 Equiv. NaOEt/EtOH 2. Mild H₂O* Br (f) i H An aldehyde 1. Catalytic NaOE/EtOH 2. H₂O*, heat 3. (CH,CH₂)₂Culi 4. Mild H₂O* 5.1.0 Equiv. LDA Br An ester 4. NaOH, H₂O 5. Mild H₂O* 6. Heat 7. MgBr 8. Mild H₂O* 7. Mild H₂O+

Chapter 19 Solutions

Chemistry: Principles and Practice

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