Chemistry (7th Edition)
7th Edition
ISBN: 9780321943170
Author: John E. McMurry, Robert C. Fay, Jill Kirsten Robinson
Publisher: PEARSON
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Question
Chapter 19, Problem 19.80SP
Interpretation Introduction
To determine:
Product of reaction
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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 19 Solutions
Chemistry (7th Edition)
Ch. 19 - Prob. 19.1PCh. 19 - Prob. 19.2ACh. 19 - Prob. 19.3PCh. 19 - Prob. 19.4PCh. 19 - Prob. 19.5PCh. 19 - Prob. 19.6ACh. 19 - Prob. 19.7PCh. 19 - Prob. 19.8ACh. 19 - Prob. 19.9PCh. 19 - Prob. 19.10A
Ch. 19 - Prob. 19.11PCh. 19 - Prob. 19.12ACh. 19 - Prob. 19.13PCh. 19 - Prob. 19.14ACh. 19 - Prob. 19.15PCh. 19 - Prob. 19.16ACh. 19 - Prob. 19.17PCh. 19 - Prob. 19.18PCh. 19 - Prob. 19.19ACh. 19 - Prob. 19.20PCh. 19 - Prob. 19.21ACh. 19 - Prob. 19.22PCh. 19 - Prob. 19.23PCh. 19 - Prob. 19.24PCh. 19 - Prob. 19.25PCh. 19 - Prob. 19.26PCh. 19 - Prob. 19.27CPCh. 19 - Prob. 19.28SPCh. 19 - Prob. 19.29SPCh. 19 - Prob. 19.30SPCh. 19 - Prob. 19.31SPCh. 19 - Prob. 19.32SPCh. 19 - Prob. 19.33SPCh. 19 - Prob. 19.34SPCh. 19 - Prob. 19.35SPCh. 19 - Prob. 19.36SPCh. 19 - Prob. 19.37SPCh. 19 - Prob. 19.38SPCh. 19 - Prob. 19.39SPCh. 19 - Prob. 19.40SPCh. 19 - Prob. 19.41SPCh. 19 - Prob. 19.42SPCh. 19 - Prob. 19.43SPCh. 19 - Prob. 19.44SPCh. 19 - Prob. 19.45SPCh. 19 - Prob. 19.46SPCh. 19 - Prob. 19.47SPCh. 19 - Prob. 19.48SPCh. 19 - Prob. 19.49SPCh. 19 - Prob. 19.50SPCh. 19 - Prob. 19.51SPCh. 19 - Prob. 19.52SPCh. 19 - Prob. 19.53SPCh. 19 - Prob. 19.54SPCh. 19 - Prob. 19.55SPCh. 19 - Prob. 19.56SPCh. 19 - Prob. 19.57SPCh. 19 - Prob. 19.58SPCh. 19 - Prob. 19.59SPCh. 19 - Prob. 19.60SPCh. 19 - Prob. 19.61SPCh. 19 - Prob. 19.62SPCh. 19 - Prob. 19.63SPCh. 19 - Prob. 19.64SPCh. 19 - Prob. 19.65SPCh. 19 - Prob. 19.66SPCh. 19 - Prob. 19.67SPCh. 19 - Prob. 19.68SPCh. 19 - Prob. 19.69SPCh. 19 - Prob. 19.70SPCh. 19 - Prob. 19.71SPCh. 19 - Prob. 19.72SPCh. 19 - Prob. 19.73SPCh. 19 - Prob. 19.74SPCh. 19 - Prob. 19.75SPCh. 19 - Prob. 19.76SPCh. 19 - Prob. 19.77SPCh. 19 - Prob. 19.78SPCh. 19 - Prob. 19.79SPCh. 19 - Prob. 19.80SPCh. 19 - Prob. 19.81SPCh. 19 - Prob. 19.82SPCh. 19 - Prob. 19.83SPCh. 19 - Prob. 19.84SPCh. 19 - Prob. 19.85SPCh. 19 - Prob. 19.86SPCh. 19 - Prob. 19.87SPCh. 19 - Prob. 19.88SPCh. 19 - Prob. 19.89SPCh. 19 - Prob. 19.90SPCh. 19 - Prob. 19.91SPCh. 19 - Prob. 19.92SPCh. 19 - Prob. 19.93SPCh. 19 - Prob. 19.94SPCh. 19 - Prob. 19.95SPCh. 19 - Prob. 19.96CPCh. 19 - Prob. 19.97CPCh. 19 - Prob. 19.98CPCh. 19 - Prob. 19.99CPCh. 19 - Prob. 19.100CPCh. 19 - Prob. 19.101CPCh. 19 - Prob. 19.102CPCh. 19 - Prob. 19.103CPCh. 19 - Prob. 19.104CPCh. 19 - Prob. 19.105CPCh. 19 - Prob. 19.106CPCh. 19 - Prob. 19.107CPCh. 19 - Prob. 19.108CPCh. 19 - Prob. 19.109CPCh. 19 - Prob. 19.110CPCh. 19 - Prob. 19.111CPCh. 19 - Prob. 19.112CPCh. 19 - Prob. 19.113MPCh. 19 - Prob. 19.114MPCh. 19 - Prob. 19.115MP
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Similar questions
- Show the mechanism for these reactionsarrow_forwardDraw the stepwise mechanismarrow_forwardDraw 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_forward
- 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
- what are the Iupac names for each structurearrow_forwardWhat are the IUPAC Names of all the compounds in the picture?arrow_forward1) 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_forward
- 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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