CHEMISTRY VOL. 2 W/MASTERING CHEM. >IC<
19th Edition
ISBN: 9781323849996
Author: Brown
Publisher: Pearson Custom Publishing
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Chapter 8, Problem 3E
A portion of a two-dimensional "slab" of NaCl(s) is shown here (see Figure 8.2) in which the ions are numbered.
- Which colored balls must represent sodium ions?
- Which colored balls must represent chloride ions?
- Consider ion 5. How many attractive electrostatic interactions are shown for it?
- Consider ion 5. How many repulsive interactions are shown for it?
- Is the sum of the attractive interactions in part (c) larger or smaller than the sum of the repulsive interactions in part (d)?
- If this pattern of ions was extended indefinitely in two dimensions, would the lattice energy be positive or negative? [Section 8.2]
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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 8 Solutions
CHEMISTRY VOL. 2 W/MASTERING CHEM. >IC<
Ch. 8.2 - Which of the these elements is most likely to from...Ch. 8.2 - Prob. 8.1.2PECh. 8.2 - Which of the following bond is the most polar? H-F...Ch. 8.2 - Prob. 8.2.2PECh. 8.3 - Prob. 8.3.1PECh. 8.3 - Prob. 8.3.2PECh. 8.4 - Which of the following bonds is the most polar? a....Ch. 8.4 - Which of the following bonds is most polar: S-Cl,...Ch. 8.4 - Prob. 8.5.1PECh. 8.4 - The dipole moment of chlorine monofluoride,...
Ch. 8.5 - Which of the these molecules has a Lewis structure...Ch. 8.5 -
How many valence electrons should appear in the...Ch. 8.5 - Compare the lewis symbol for neon the structure...Ch. 8.5 - Prob. 8.7.2PECh. 8.5 - Prob. 8.8.1PECh. 8.5 - Prob. 8.8.2PECh. 8.5 - Prob. 8.9.1PECh. 8.5 - Prob. 8.9.2PECh. 8.6 - Which of the statements about resonance is true?...Ch. 8.6 - Prob. 8.10.2PECh. 8.7 - Prob. 8.11.1PECh. 8.7 - Prob. 8.11.2PECh. 8 - Prob. 1DECh. 8 - Prob. 1ECh. 8 - Prob. 2ECh. 8 - A portion of a two-dimensional "slab" of NaCl(s)...Ch. 8 - Prob. 4ECh. 8 - Prob. 5ECh. 8 - Incomplete Lewis structures for the nitrous acid...Ch. 8 - Prob. 7ECh. 8 - Prob. 8ECh. 8 - Prob. 9ECh. 8 - True or false: The hydrogen atom is most stable...Ch. 8 - Consider the element silicon, Si. Write its...Ch. 8 - Write the electron configuration for the element...Ch. 8 - Prob. 13ECh. 8 - What is the Lewis symbol for each of the following...Ch. 8 - Using Lewis symbols, diagram the reaction between...Ch. 8 - Use Lewis symbols to represent the reaction that...Ch. 8 - Predict the chemical formula of the ionic compound...Ch. 8 - Prob. 18ECh. 8 - Prob. 19ECh. 8 - Prob. 20ECh. 8 - Is lattice energy usually endothermic or...Ch. 8 - NaCI and KF have the same crystal structure. The...Ch. 8 - Prob. 23ECh. 8 - Prob. 24ECh. 8 - Consider the ionic compounds KF, NaCl, NaBr, and...Ch. 8 - Which of the following trends in lattice energy is...Ch. 8 - Energy is required to remove two electrons from Ca...Ch. 8 - Prob. 28ECh. 8 - Use data from Appendix C, Figure 7.10, and Figure...Ch. 8 - Prob. 30ECh. 8 - Prob. 31ECh. 8 - Prob. 32ECh. 8 - Using Lewis symbols and Lewis structures, diagram...Ch. 8 - Use Lewis symbols and Lewis structures to diagram...Ch. 8 - Prob. 35ECh. 8 - Prob. 36ECh. 8 - Prob. 37ECh. 8 - What is the trend in electronegativity going from...Ch. 8 - Prob. 39ECh. 8 - By referring only to the periodic table, select...Ch. 8 - which of the following bonds are polar? B-F,...Ch. 8 - Arrange the bonds in each of the following sets in...Ch. 8 - Prob. 43ECh. 8 - Prob. 44ECh. 8 - In the following pairs of binary compounds,...Ch. 8 - Prob. 46ECh. 8 - Prob. 47ECh. 8 - Write Lewis structures for the following: H2CO...Ch. 8 - Prob. 49ECh. 8 - Draw the dominant Lewis structure for the...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - Prob. 52ECh. 8 - Prob. 53ECh. 8 - Prob. 54ECh. 8 - Prob. 55ECh. 8 - Prob. 56ECh. 8 - Prob. 57ECh. 8 - Prob. 58ECh. 8 - Prob. 59ECh. 8 - Prob. 60ECh. 8 - Prob. 61ECh. 8 - 8.62 For Group 3A-7A elements in the third row of...Ch. 8 - Draw the Lewis structures for each of the...Ch. 8 - Prob. 64ECh. 8 - In the vapor phase, BeCl2exists as a discrete...Ch. 8 -
8.66
Describe the molecule xenon trioxide, XeO3,...Ch. 8 -
8.67 There are many Lewis structures you could...Ch. 8 - Prob. 68ECh. 8 - Using Table 8.3, estimate H for each of the...Ch. 8 - Using Table 8.3, estimate H for the following...Ch. 8 - State whether each of these statements is true or...Ch. 8 - Prob. 72ECh. 8 - Prob. 73ECh. 8 - Prob. 74ECh. 8 - Prob. 75ECh. 8 - Prob. 76ECh. 8 - A new compound is made that has a C-C bond length...Ch. 8 - A new compound is made that has an N-N bond length...Ch. 8 - Prob. 79AECh. 8 - Prob. 80AECh. 8 - An ionic substance of formula MX has a lattice...Ch. 8 - Prob. 82AECh. 8 - Prob. 83AECh. 8 - Prob. 84AECh. 8 - Consider the collection of nonmetallic elements 0,...Ch. 8 - The substance chlorine monoxide, CIO(g), is...Ch. 8 -
[8.87]
a. using the electronegativities of Br...Ch. 8 - Prob. 88AECh. 8 - Although I3- is a known ion, F3- is not. a. Draw...Ch. 8 - Calculate the formal charge on the indicated atom...Ch. 8 - The hypochlorite ion, CIO- , is the active...Ch. 8 - Prob. 92AECh. 8 - a. Triazine, C3 H3N3, is like benzene except that...Ch. 8 - Prob. 94IECh. 8 - Prob. 95IECh. 8 - Prob. 96IECh. 8 - Prob. 97IECh. 8 - Prob. 98IECh. 8 - Prob. 99IECh. 8 - Prob. 100IECh. 8 - Prob. 101IECh. 8 - Prob. 102IECh. 8 -
8.103 The compound chloral hydrate, known in...Ch. 8 - Barium azide is 62.04% Ba and 37.96% N. Each azide...Ch. 8 - Acetylene (C2H2) and nitrogen (N2) both contain a...Ch. 8 - Prob. 106IECh. 8 - Prob. 107IECh. 8 -
8.108 Formic acid has the chemical formula...Ch. 8 - Prob. 109IECh. 8 - Prob. 110IE
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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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