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 21, Problem 21.100SP
(a)
Interpretation Introduction
To determine:
Calculated by silicon wavelength
(b)
Interpretation Introduction
To determine:
Whether the wavelength of silicon corresponds to the highest intensity wavelength in the solar emission spectrum
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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 21 Solutions
Chemistry (7th Edition)
Ch. 21 - Prob. 21.1PCh. 21 - Prob. 21.2PCh. 21 - Prob. 21.3PCh. 21 - Prob. 21.4ACh. 21 - Prob. 21.5PCh. 21 - Prob. 21.6ACh. 21 - Prob. 21.7PCh. 21 - Prob. 21.8PCh. 21 - Prob. 21.9ACh. 21 - Prob. 21.10P
Ch. 21 - Prob. 21.11PCh. 21 - Prob. 21.12CPCh. 21 - Prob. 21.13CPCh. 21 - Prob. 21.14CPCh. 21 - Prob. 21.15PCh. 21 - Prob. 21.16CPCh. 21 - Prob. 21.17CPCh. 21 - Prob. 21.18CPCh. 21 - Prob. 21.19CPCh. 21 - Prob. 21.20CPCh. 21 - Prob. 21.21CPCh. 21 - Prob. 21.22CPCh. 21 - Prob. 21.23CPCh. 21 - Prob. 21.24SPCh. 21 - Prob. 21.25SPCh. 21 - Prob. 21.26SPCh. 21 - Prob. 21.27SPCh. 21 - Prob. 21.28SPCh. 21 - Prob. 21.29SPCh. 21 - Prob. 21.30SPCh. 21 - Prob. 21.31SPCh. 21 - Describe the flotation process for concentrating a...Ch. 21 - Prob. 21.33SPCh. 21 - Prob. 21.34SPCh. 21 - Prob. 21.35SPCh. 21 - Prob. 21.36SPCh. 21 - Prob. 21.37SPCh. 21 - Prob. 21.38SPCh. 21 - Prob. 21.39SPCh. 21 - Prob. 21.40SPCh. 21 - Prob. 21.41SPCh. 21 - Prob. 21.42SPCh. 21 - Prob. 21.43SPCh. 21 - Prob. 21.44SPCh. 21 - Pure copper for use in electrical wiring is...Ch. 21 - Prob. 21.46SPCh. 21 - Prob. 21.47SPCh. 21 - Prob. 21.48SPCh. 21 - Prob. 21.49SPCh. 21 - Prob. 21.50SPCh. 21 - Prob. 21.51SPCh. 21 - Prob. 21.52SPCh. 21 - Prob. 21.53SPCh. 21 - Prob. 21.54SPCh. 21 - Prob. 21.55SPCh. 21 - Prob. 21.56SPCh. 21 - Prob. 21.57SPCh. 21 - Prob. 21.58SPCh. 21 - Prob. 21.59SPCh. 21 - Prob. 21.60SPCh. 21 - Prob. 21.61SPCh. 21 - Prob. 21.62SPCh. 21 - Prob. 21.63SPCh. 21 - Prob. 21.64SPCh. 21 - Prob. 21.65SPCh. 21 - Prob. 21.66SPCh. 21 - Prob. 21.67SPCh. 21 - Prob. 21.68SPCh. 21 - Prob. 21.69SPCh. 21 - Prob. 21.70SPCh. 21 - Prob. 21.71SPCh. 21 - The melting points for the second-series...Ch. 21 - Copper has a Mohs hardness value of 3, and iron...Ch. 21 - Prob. 21.74SPCh. 21 - Prob. 21.75SPCh. 21 - Prob. 21.76SPCh. 21 - Prob. 21.77SPCh. 21 - Prob. 21.78SPCh. 21 - Prob. 21.79SPCh. 21 - Prob. 21.80SPCh. 21 - Prob. 21.81SPCh. 21 - Prob. 21.82SPCh. 21 - Prob. 21.83SPCh. 21 - Prob. 21.84SPCh. 21 - Prob. 21.85SPCh. 21 - Prob. 21.86SPCh. 21 - Prob. 21.87SPCh. 21 - Prob. 21.88SPCh. 21 - Prob. 21.89SPCh. 21 - Prob. 21.90SPCh. 21 - Prob. 21.91SPCh. 21 - Prob. 21.92SPCh. 21 - Prob. 21.93SPCh. 21 - Prob. 21.94SPCh. 21 - Prob. 21.95SPCh. 21 - Prob. 21.96SPCh. 21 - Prob. 21.97SPCh. 21 - Prob. 21.98SPCh. 21 - Prob. 21.99SPCh. 21 - Prob. 21.100SPCh. 21 - Prob. 21.101SPCh. 21 - Prob. 21.102SPCh. 21 - Prob. 21.103SPCh. 21 - Prob. 21.104SPCh. 21 - Prob. 21.105SPCh. 21 - Prob. 21.106SPCh. 21 - Prob. 21.107SPCh. 21 - Prob. 21.108SPCh. 21 - Why are oxide ceramics more corrosion-resistant...Ch. 21 - Prob. 21.110SPCh. 21 - Prob. 21.111SPCh. 21 - Prob. 21.112SPCh. 21 - Prob. 21.113SPCh. 21 - Prob. 21.114SPCh. 21 - Prob. 21.115SPCh. 21 - Prob. 21.116SPCh. 21 - Prob. 21.117SPCh. 21 - Prob. 21.118SPCh. 21 - Prob. 21.119SPCh. 21 - Prob. 21.120SPCh. 21 - Prob. 21.121SPCh. 21 - Prob. 21.122SPCh. 21 - Prob. 21.123SPCh. 21 - Prob. 21.124CPCh. 21 - Prob. 21.125CPCh. 21 - Prob. 21.126CPCh. 21 - Prob. 21.127CPCh. 21 - Prob. 21.128CPCh. 21 - Prob. 21.129CPCh. 21 - Prob. 21.130CPCh. 21 - Prob. 21.131CPCh. 21 - Prob. 21.132CPCh. 21 - Prob. 21.133CPCh. 21 - Gallium arsenide, a material used to manufacture...Ch. 21 - Prob. 21.135CPCh. 21 - Prob. 21.136CPCh. 21 - Prob. 21.137CPCh. 21 - Prob. 21.138CPCh. 21 - Prob. 21.139CPCh. 21 - Prob. 21.141CPCh. 21 - Prob. 21.142CPCh. 21 - Prob. 21.143CPCh. 21 - Prob. 21.144CPCh. 21 - Prob. 21.145MPCh. 21 - Prob. 21.146MPCh. 21 - Prob. 21.147MPCh. 21 - light with a wavelength of 660 nm from a 3.0 mW...Ch. 21 - Prob. 21.149MPCh. 21 - Prob. 21.150MPCh. 21 - Prob. 21.151MPCh. 21 - Prob. 21.152MPCh. 21 - Prob. 21.153MPCh. 21 - Prob. 21.154MPCh. 21 - Prob. 21.155MP
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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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