Chemistry Atoms First2e
2nd Edition
ISBN: 9781947172647
Author: OpenStax
Publisher: OpenStax College
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Chapter 5, Problem 30E
Sketch the distribution of electron density in the bonding and antibonding molecular orbitals formed form two s orbitals and from two p orbitals.
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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 5 Solutions
Chemistry Atoms First2e
Ch. 5 - Explain how σ and bonds are similar and how they...Ch. 5 - Use valence bond theory to explain the bonding in...Ch. 5 - Use valence bond theory to explain the bonding in...Ch. 5 - How many and bonds are present in the molecule...Ch. 5 - A friend tell you N2 has three bonds due to...Ch. 5 - Draw the Lewis Structures for CO2andCO , and...Ch. 5 - Why is the concept of hybridization required in...Ch. 5 - Give the shape that describes each hybrid orbital...Ch. 5 - Explain why a carbon atom cannot from five bonds...Ch. 5 - What is the hybridization of the central atom in...
Ch. 5 - A molecule with the formula AB3 could have one of...Ch. 5 - Methionine, CH3SCH2CH2CH(NH2)CO2H, is an amino...Ch. 5 - Sulfuric acid is manufactured by a series of...Ch. 5 - Two important industrial chemicals,...Ch. 5 - Analysis of a compound indicates that it contains...Ch. 5 - Consider nitrous acid, HNO2(HONO). (a) Write a...Ch. 5 - Strike-anywhere matches contain a layer of KC1O3...Ch. 5 - Identify the hybridization of each carbon atom in...Ch. 5 - Write Lewis structures for NF3andPF5 . On the...Ch. 5 - In addition to NF3, two other fluoro derivatives...Ch. 5 - The bond energy of a C-C single bond averages...Ch. 5 - For the carbonate ion, CO32 -, draw all of the...Ch. 5 - A useful solvent that will dissolve salts as well...Ch. 5 - For the molecule allene, H2C=C=CH2, give the...Ch. 5 - Identify the hybridization of the central atom in...Ch. 5 - Describe the molecular geometry and hybridization...Ch. 5 - For each of the following molecules, indicate the...Ch. 5 - For each of the following structures, determine...Ch. 5 - Draw the orbital diagram for carbon in CO2 showing...Ch. 5 - Sketch the distribution of electron density in the...Ch. 5 - How are the following similar, and how do they...Ch. 5 - If molecular orbitals are created by combining...Ch. 5 - Can a molecule with an odd number of electrons...Ch. 5 - Can a molecule with an even number of electrons...Ch. 5 - Why are bonding molecular orbital lower in energy...Ch. 5 - Calculate the bond order for an ion with this...Ch. 5 - Explain why an electron in the bonding molecular...Ch. 5 - Predict the valence electron molecular orbital...Ch. 5 - Determine the bond order of each member of the...Ch. 5 - For the first ionizations energy for an N2...Ch. 5 - Compare the atomic and molecular orbitaI diagrams...Ch. 5 - Which of the period 2 homonuclear diatomic...Ch. 5 - A friend tells you that the 2s orbital for...Ch. 5 - True or false: Boron contains 2s22p1 valence...Ch. 5 - What charge would be needed on F2 to generate an...Ch. 5 - Predict whether the MO diagram for S2 would show...Ch. 5 - Explain why N22+ is diamagnetic, while O24+, which...Ch. 5 - Using the MO diagrams, predict the bond order for...
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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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