
Chemistry: A Molecular Approach (4th Edition)
4th Edition
ISBN: 9780134112831
Author: Nivaldo J. Tro
Publisher: PEARSON
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Chapter 10, Problem 10E
Interpretation Introduction
Interpretation: The interaction between the electron and nucleus of one electrons of another atom.
Concept Introduction:
In
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Part I.
a)
Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone
b) Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone
(3,3-dimethyl-2-butanone) and 2, 3-dimethyl - 1,3-butadiene. Give reasonable mechanism
the formation of
the products
For
3. The explosive decomposition of 2 mole of TNT (2,4,6-trinitrotoluene) is shown below:
Assume the C(s) is soot-basically atomic carbon (although it isn't actually atomic carbon in real life).
2
CH3
H
NO2
NO2
3N2 (g)+7CO (g) + 5H₂O (g) + 7C (s)
H
a. Use bond dissociation energies to calculate how much AU is for this reaction in kJ/mol.
Part I.
Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff:
Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone
and
(3,3-dimethyl-2-butanone) 2,3-dimethyl-1,3-butadiene. Give reasonable mechanism
the formation of the products
For
Chapter 10 Solutions
Chemistry: A Molecular Approach (4th Edition)
Ch. 10 - Prob. 1SAQCh. 10 - Prob. 2SAQCh. 10 - Prob. 3SAQCh. 10 - Prob. 4SAQCh. 10 - Prob. 5SAQCh. 10 - Prob. 6SAQCh. 10 - Prob. 7SAQCh. 10 - Prob. 8SAQCh. 10 - Prob. 9SAQCh. 10 - Q10. Apply molecular orbital theory to predict...
Ch. 10 - Q11. Apply molecular orbital theory to determine...Ch. 10 - Q12. Which hybridization scheme occurs about...Ch. 10 - Q13. Which molecular geometry results when a...Ch. 10 - Prob. 14SAQCh. 10 - Prob. 15SAQCh. 10 - 1. Why is molecular geometry important? Cite some...Ch. 10 - 2. According to VSEPR theory, what determines the...Ch. 10 - 3. Name and sketch the five basic electron...Ch. 10 - 4. Explain the difference between electron...Ch. 10 - 5. Give the correct electron and molecular...Ch. 10 - 6. How do you apply VSEPR theory to predict the...Ch. 10 - Prob. 7ECh. 10 - Prob. 8ECh. 10 - 9. In valence bond theory, what determines the...Ch. 10 - 10. In valence bond theory, the interaction energy...Ch. 10 - Prob. 11ECh. 10 - Prob. 12ECh. 10 - 13. How is the number of hybrid orbitals related...Ch. 10 - Prob. 14ECh. 10 - Prob. 15ECh. 10 - 16. Name the hybridization scheme that corresponds...Ch. 10 - Prob. 17ECh. 10 - Prob. 18ECh. 10 - 19. What is a bonding molecular orbital?
Ch. 10 - 20. What is an antibonding molecular orbital?
Ch. 10 - 21. What is the role of wave interference in...Ch. 10 - Prob. 22ECh. 10 - 23. How is the number of molecular orbitals...Ch. 10 - 24. Sketch each molecular orbital.
a. σ2s
b.
c....Ch. 10 - Prob. 25ECh. 10 - Prob. 26ECh. 10 - Prob. 27ECh. 10 - Prob. 28ECh. 10 - Prob. 29ECh. 10 - 30. Write a short paragraph describing chemical...Ch. 10 - 31. A molecule with the formula AB3 has a trigonal...Ch. 10 - 32. A molecule with the formula AB3 has a trigonal...Ch. 10 - 33. For each molecular geometry, list the number...Ch. 10 - Prob. 34ECh. 10 - 35. Determine the electron geometry, molecular...Ch. 10 - 36. Determine the electron geometry, molecular...Ch. 10 - 37. Which species has the smaller bond angle, H3O...Ch. 10 - Prob. 38ECh. 10 - 39. Determine the molecular geometry and sketch...Ch. 10 - Prob. 40ECh. 10 - Prob. 41ECh. 10 - Prob. 42ECh. 10 - 43. Each ball-and-stick model shows the electron...Ch. 10 - 44. Each ball-and-stick model shows the electron...Ch. 10 - 45. Determine the geometry about each interior...Ch. 10 - Prob. 46ECh. 10 - Prob. 47ECh. 10 - Prob. 48ECh. 10 - Prob. 49ECh. 10 - Prob. 50ECh. 10 - 51. Determine whether each molecule is polar or...Ch. 10 - Prob. 52ECh. 10 - 53. The valence electron configurations of several...Ch. 10 - 54. The valence electron configurations of several...Ch. 10 - 55. Write orbital diagrams (boxes with arrows in...Ch. 10 - Prob. 56ECh. 10 - 57. Write orbital diagrams (boxes with arrows in...Ch. 10 - Prob. 58ECh. 10 - 59. Which hybridization scheme allows the...Ch. 10 - Prob. 60ECh. 10 - Prob. 61ECh. 10 - 62. Write a hybridization and bonding scheme for...Ch. 10 - Prob. 63ECh. 10 - 64. Write a hybridization and bonding scheme for...Ch. 10 - 65. Write a hybridization and bonding scheme for...Ch. 10 - Prob. 66ECh. 10 - 67. Consider the structure of the amino acid...Ch. 10 - 68. Consider the structure of the amino acid...Ch. 10 - 69. Sketch the bonding molecular orbital that...Ch. 10 - Prob. 70ECh. 10 - 71. Draw an MO energy diagram and predict the bond...Ch. 10 - Prob. 72ECh. 10 - Prob. 73ECh. 10 - Prob. 74ECh. 10 - Prob. 75ECh. 10 - 76. Using the molecular orbital energy ordering...Ch. 10 - 77. Use molecular orbital theory to predict if...Ch. 10 - 78. Use molecular orbital theory to predict if...Ch. 10 - Prob. 79ECh. 10 - Prob. 80ECh. 10 - 81. Draw an MO energy diagram for CO. (Use the...Ch. 10 - Prob. 82ECh. 10 - 83. For each compound, draw the Lewis structure,...Ch. 10 - 84. For each compound, draw the Lewis structure,...Ch. 10 - 85. Amino acids are biological compounds that link...Ch. 10 - 86. The genetic code is based on four different...Ch. 10 - 87. The structure of caffeine, present in coffee...Ch. 10 - 88. The structure of acetylsalicylic acid...Ch. 10 - 89. Most vitamins can be classified as either fat...Ch. 10 - 90. Water does not easily remove grease from...Ch. 10 - Prob. 91ECh. 10 - Prob. 92ECh. 10 - 93. Bromine can form compounds or ions with any...Ch. 10 - 94. The compound C3H4 has two double bonds....Ch. 10 - Prob. 95ECh. 10 - Prob. 96ECh. 10 - Prob. 97ECh. 10 - 98. Indicate which orbitals overlap to form the s...Ch. 10 - 99. In VSEPR theory, which uses the Lewis model to...Ch. 10 - 100. The results of a molecular orbital...Ch. 10 - 101. The results of a molecular orbital...Ch. 10 - Prob. 102ECh. 10 - Prob. 103ECh. 10 - Prob. 104ECh. 10 - Prob. 105ECh. 10 - 106. Neither the VSEPR model nor the hybridization...Ch. 10 - 107. Draw the Lewis structure for acetamide...Ch. 10 - Prob. 108ECh. 10 - 109. Which statement best captures the fundamental...Ch. 10 - 110. Suppose that a molecule has four bonding...Ch. 10 - 111. How does each of the three major bonding...Ch. 10 - Prob. 112ECh. 10 - Prob. 113QGWCh. 10 - Prob. 114QGWCh. 10 - Prob. 115QGWCh. 10 - Prob. 116QGWCh. 10 - Prob. 117QGWCh. 10 - Prob. 118DIA
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- Draw the stepwise mechanism for the reactionsarrow_forwardDraw stepwise mechanismarrow_forwardPart I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: a) Give the major reason for the exposure of benzophenone al isopropyl alcohol (w/acid) to direct sunlight of pina colone Mechanism For b) Pinacol (2,3-dimethy 1, 1-3-butanediol) on treatment w/ acid gives a mixture (3,3-dimethyl-2-butanone) and 2, 3-dimethyl-1,3-butadiene. Give reasonable the formation of the productsarrow_forward
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- 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+arrow_forwardLi+ is a hard acid. With this in mind, which if the following compounds should be most soluble in water? Group of answer choices LiBr LiI LiF LiClarrow_forwardQ4: Write organic product(s) of the following reactions and show the curved-arrow mechanism of the reactions. Br MeOH OSO2CH3 MeOHarrow_forward
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