PHYSICAL CHEMISTRY. VOL.1+2 (LL)(11TH)
11th Edition
ISBN: 9780198826910
Author: ATKINS
Publisher: Oxford University Press
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Chapter 15, Problem 15B.1BE
Interpretation Introduction
Interpretation:
The wavelength of the X-rays under given condition has to be calculated.
Concept Introduction:
Bragg’s law:
It relates the angle of a diffracted beam to the spacing of a given set of lattice planes. Mathematically it can be represented as
Where,
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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 15 Solutions
PHYSICAL CHEMISTRY. VOL.1+2 (LL)(11TH)
Ch. 15 - Prob. 15A.1STCh. 15 - Prob. 15B.1STCh. 15 - Prob. 15B.3STCh. 15 - Prob. 15C.1STCh. 15 - Prob. 15C.2STCh. 15 - Prob. 15A.1DQCh. 15 - Prob. 15A.2DQCh. 15 - Prob. 15A.3DQCh. 15 - Prob. 15A.1AECh. 15 - Prob. 15A.1BE
Ch. 15 - Prob. 15A.2AECh. 15 - Prob. 15A.2BECh. 15 - Prob. 15A.3AECh. 15 - Prob. 15A.3BECh. 15 - Prob. 15A.4AECh. 15 - Prob. 15A.4BECh. 15 - Prob. 15A.1PCh. 15 - Prob. 15A.2PCh. 15 - Prob. 15A.3PCh. 15 - Prob. 15A.4PCh. 15 - Prob. 15A.5PCh. 15 - Prob. 15A.6PCh. 15 - Prob. 15A.7PCh. 15 - Prob. 15A.8PCh. 15 - Prob. 15A.9PCh. 15 - Prob. 15B.1DQCh. 15 - Prob. 15B.2DQCh. 15 - Prob. 15B.3DQCh. 15 - Prob. 15B.1AECh. 15 - Prob. 15B.1BECh. 15 - Prob. 15B.2AECh. 15 - Prob. 15B.2BECh. 15 - Prob. 15B.3AECh. 15 - Prob. 15B.3BECh. 15 - Prob. 15B.4AECh. 15 - Prob. 15B.4BECh. 15 - Prob. 15B.5AECh. 15 - Prob. 15B.5BECh. 15 - Prob. 15B.6AECh. 15 - Prob. 15B.6BECh. 15 - Prob. 15B.7AECh. 15 - Prob. 15B.7BECh. 15 - Prob. 15B.11AECh. 15 - Prob. 15B.11BECh. 15 - Prob. 15B.12AECh. 15 - Prob. 15B.12BECh. 15 - Prob. 15B.1PCh. 15 - Prob. 15B.2PCh. 15 - Prob. 15B.3PCh. 15 - Prob. 15B.4PCh. 15 - Prob. 15B.6PCh. 15 - Prob. 15B.7PCh. 15 - Prob. 15C.1DQCh. 15 - Prob. 15C.2DQCh. 15 - Prob. 15C.1AECh. 15 - Prob. 15C.2AECh. 15 - Prob. 15C.2BECh. 15 - Prob. 15C.3AECh. 15 - Prob. 15C.3BECh. 15 - Prob. 15C.4AECh. 15 - Prob. 15C.4BECh. 15 - Prob. 15C.5AECh. 15 - Prob. 15C.5BECh. 15 - Prob. 15C.1PCh. 15 - Prob. 15C.2PCh. 15 - Prob. 15C.3PCh. 15 - Prob. 15C.4PCh. 15 - Prob. 15C.5PCh. 15 - Prob. 15C.7PCh. 15 - Prob. 15C.8PCh. 15 - Prob. 15C.9PCh. 15 - Prob. 15D.1DQCh. 15 - Prob. 15D.1AECh. 15 - Prob. 15D.1BECh. 15 - Prob. 15D.2AECh. 15 - Prob. 15D.2BECh. 15 - Prob. 15D.3AECh. 15 - Prob. 15D.3BECh. 15 - Prob. 15D.1PCh. 15 - Prob. 15D.2PCh. 15 - Prob. 15E.1DQCh. 15 - Prob. 15E.1AECh. 15 - Prob. 15E.1BECh. 15 - Prob. 15E.2AECh. 15 - Prob. 15E.2BECh. 15 - Prob. 15E.3AECh. 15 - Prob. 15E.3BECh. 15 - Prob. 15E.5PCh. 15 - Prob. 15F.1DQCh. 15 - Prob. 15F.1AECh. 15 - Prob. 15F.1BECh. 15 - Prob. 15F.2AECh. 15 - Prob. 15F.2BECh. 15 - Prob. 15F.3AECh. 15 - Prob. 15F.3BECh. 15 - Prob. 15F.4AECh. 15 - Prob. 15F.4BECh. 15 - Prob. 15F.5AECh. 15 - Prob. 15F.5BECh. 15 - Prob. 15G.1DQCh. 15 - Prob. 15G.2DQCh. 15 - Prob. 15G.1AECh. 15 - Prob. 15G.1BECh. 15 - Prob. 15.1IA
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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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