Student Solutions Manual for Ball's Physical Chemistry, 2nd
2nd Edition
ISBN: 9798214169019
Author: David W. Ball
Publisher: Cengage Learning US
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Chapter 12, Problem 12.4E
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Draw the stepwise mechanism for the reactions
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.
Chapter 12 Solutions
Student Solutions Manual for Ball's Physical Chemistry, 2nd
Ch. 12 - In the Stern-Gerlach experiment, silver atoms were...Ch. 12 - Prob. 12.2ECh. 12 - Prob. 12.3ECh. 12 - Suppose s=12 for an electron. Into how many parts...Ch. 12 - Using and labels, write two possible...Ch. 12 - List all possible combinations of all four quantum...Ch. 12 - What are the degeneracies of the H atom...Ch. 12 - Prob. 12.8ECh. 12 - a Differentiate between the quantum numbers s and...Ch. 12 - Is the spin orbital 1s for the H atom still...
Ch. 12 - Draw a diagram analogous to Figure 11.15, but now...Ch. 12 - Are mathematical expressions for the following...Ch. 12 - Prob. 12.13ECh. 12 - Prob. 12.14ECh. 12 - a Assume that the electronic energy of Li was a...Ch. 12 - Spin orbitals are products of spatial and spin...Ch. 12 - If 1 and 2 are the individual wavefunctions for...Ch. 12 - Show that the correct behavior of a wavefunction...Ch. 12 - Prob. 12.19ECh. 12 - Why isnt the electron configuration of beryllium,...Ch. 12 - Prob. 12.21ECh. 12 - Write a Slater determinant for the lithide ion,...Ch. 12 - Why does the concept of antisymmetric...Ch. 12 - a Construct Slater determinant wavefunctions for...Ch. 12 - Prob. 12.25ECh. 12 - Prob. 12.26ECh. 12 - Prob. 12.27ECh. 12 - Suppose an electron had three possible values of...Ch. 12 - Using a periodic table or Table 12.1, find the...Ch. 12 - Write an acceptable electron configuration for...Ch. 12 - Prob. 12.31ECh. 12 - Prob. 12.32ECh. 12 - Prob. 12.33ECh. 12 - An anharmonic oscillator has the potential...Ch. 12 - Prob. 12.35ECh. 12 - In a particle-in-a-box having length a, the...Ch. 12 - Prob. 12.37ECh. 12 - Prob. 12.38ECh. 12 - Prob. 12.39ECh. 12 - The Stark effect is the change in energy of a...Ch. 12 - Prob. 12.41ECh. 12 - Prob. 12.42ECh. 12 - Prob. 12.43ECh. 12 - Show that a variation theory treatment of H using...Ch. 12 - Prob. 12.45ECh. 12 - Explain why assuming an effective nuclear charge,...Ch. 12 - Prob. 12.47ECh. 12 - Consider a real system. Assume that a real...Ch. 12 - Prob. 12.49ECh. 12 - Prob. 12.50ECh. 12 - Prob. 12.51ECh. 12 - Prob. 12.52ECh. 12 - State the Born-Oppenheimer approximation in words...Ch. 12 - Prob. 12.54ECh. 12 - Spectroscopy deals with differences in energy...Ch. 12 - Prob. 12.56ECh. 12 - What is the bond order for the lowest excited...Ch. 12 - The helium atom was defined as two electrons and a...Ch. 12 - Explain how we know that the first in equation...Ch. 12 - Prob. 12.60ECh. 12 - Prob. 12.61ECh. 12 - Use molecular orbital arguments to decide whether...Ch. 12 - Prob. 12.63ECh. 12 - Prob. 12.65ECh. 12 - Prob. 12.67ECh. 12 - Prob. 12.68E
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- 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 Forarrow_forwardShow the mechanism for these reactionsarrow_forwardDraw the stepwise mechanismarrow_forward
- Draw a structural formula of the principal product formed when benzonitrile is treated with each reagent. (a) H₂O (one equivalent), H₂SO₄, heat (b) H₂O (excess), H₂SO₄, heat (c) NaOH, H₂O, heat (d) LiAlH4, then H₂Oarrow_forwardDraw the stepwise mechanism for the reactionsarrow_forwardDraw stepwise mechanismarrow_forward
- Part 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_forwardwhat are the Iupac names for each structurearrow_forwardWhat are the IUPAC Names of all the compounds in the picture?arrow_forward
- 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)arrow_forward19.78 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_forward
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