Chemistry for Today: General, Organic, and Biochemistry
9th Edition
ISBN: 9781305960060
Author: Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher: Cengage Learning
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Question
Chapter 10, Problem 10.68E
Interpretation Introduction
Interpretation:
The product that has the most penetrating radiation is to be stated.
Concept Introduction:
Radioactive decay is the process that involves the emission of radiation by an unstable atomic nucleus. The atomic nucleus loses it energy. The process is spontaneous. It is also known as nuclear radiation.
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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 10 Solutions
Chemistry for Today: General, Organic, and Biochemistry
Ch. 10 - Prob. 10.1ECh. 10 - Prob. 10.2ECh. 10 - Prob. 10.3ECh. 10 - Prob. 10.4ECh. 10 - Prob. 10.5ECh. 10 - Prob. 10.6ECh. 10 - Write appropriate symbols for the following...Ch. 10 - Prob. 10.8ECh. 10 - Prob. 10.9ECh. 10 - Prob. 10.10E
Ch. 10 - Prob. 10.11ECh. 10 - Prob. 10.12ECh. 10 - Prob. 10.13ECh. 10 - Prob. 10.14ECh. 10 - Prob. 10.15ECh. 10 - Prob. 10.16ECh. 10 - Prob. 10.17ECh. 10 - Prob. 10.18ECh. 10 - Prob. 10.19ECh. 10 - Prob. 10.20ECh. 10 - Prob. 10.21ECh. 10 - Prob. 10.22ECh. 10 - Prob. 10.23ECh. 10 - Prob. 10.24ECh. 10 - Prob. 10.25ECh. 10 - Prob. 10.26ECh. 10 - Prob. 10.27ECh. 10 - Prob. 10.28ECh. 10 - Prob. 10.29ECh. 10 - Prob. 10.30ECh. 10 - Prob. 10.31ECh. 10 - Prob. 10.32ECh. 10 - Prob. 10.33ECh. 10 - Prob. 10.34ECh. 10 - Prob. 10.35ECh. 10 - Prob. 10.36ECh. 10 - Prob. 10.37ECh. 10 - Prob. 10.38ECh. 10 - Prob. 10.39ECh. 10 - Prob. 10.40ECh. 10 - Prob. 10.41ECh. 10 - Prob. 10.42ECh. 10 - Prob. 10.43ECh. 10 - Prob. 10.44ECh. 10 - Prob. 10.45ECh. 10 - Prob. 10.46ECh. 10 - Prob. 10.47ECh. 10 - Prob. 10.48ECh. 10 - Prob. 10.49ECh. 10 - Prob. 10.50ECh. 10 - Prob. 10.51ECh. 10 - Prob. 10.52ECh. 10 - Prob. 10.53ECh. 10 - Prob. 10.54ECh. 10 - Prob. 10.55ECh. 10 - Prob. 10.56ECh. 10 - Prob. 10.57ECh. 10 - Prob. 10.58ECh. 10 - Prob. 10.59ECh. 10 - Prob. 10.60ECh. 10 - Prob. 10.61ECh. 10 - Prob. 10.62ECh. 10 - Prob. 10.63ECh. 10 - Prob. 10.64ECh. 10 - Prob. 10.65ECh. 10 - Prob. 10.66ECh. 10 - Prob. 10.67ECh. 10 - Prob. 10.68ECh. 10 - Prob. 10.69ECh. 10 - Prob. 10.70ECh. 10 - Prob. 10.71ECh. 10 - Prob. 10.72ECh. 10 - Prob. 10.73ECh. 10 - Prob. 10.74ECh. 10 - Prob. 10.75ECh. 10 - Prob. 10.76ECh. 10 - Prob. 10.77ECh. 10 - Prob. 10.78ECh. 10 - Prob. 10.79ECh. 10 - Prob. 10.80ECh. 10 - Prob. 10.81ECh. 10 - Prob. 10.82ECh. 10 - Prob. 10.83ECh. 10 - Prob. 10.84ECh. 10 - Prob. 10.85ECh. 10 - Prob. 10.86E
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Similar questions
- 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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