
CHEMISITRY W/OWL PKG LOOSELEAF
9th Edition
ISBN: 9781285903859
Author: ZUMDAHL
Publisher: CENGAGE L
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Chapter 9, Problem 69AE
Interpretation Introduction
Interpretation: The barrier rotation of carbon-carbon double bond is to be estimated.
Concept introduction: In any molecule, single bonds rotate easily due to head-to-head overlapping of orbitals. But rotation of double bond is restricted. In double bond electron density above and below the plane is very high. This high density cause repulsion between electrons and restrict rotation.
To determine: The given structures are same or not.
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For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check
the appropriate box.
Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below.
Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions
- just focus on the first stable product you expect to form in solution.
?
NH2
MgBr
Will the first product that forms in this reaction
create a new CC bond?
○ Yes
○ No
MgBr
?
Will the first product that forms in this reaction
create a new CC bond?
O Yes
O No
Click and drag to start drawing a
structure.
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x
c
olo
Ar
HE
Predicting
As the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule
with a new C - C bond as its major product:
H₂N
O
H
1.
?
2. H3O+
If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more
than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for
example to distinguish between major products with different stereochemistry.
0
If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank.
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Explanation
Check
Click and drag to start drawing a
structure.
Highlight the chirality (or stereogenic) center(s) in the given compound. A compound may have one or more stereogenic centers.
OH
OH
OH
OH
OH
OH
Chapter 9 Solutions
CHEMISITRY W/OWL PKG LOOSELEAF
Ch. 9 - Why do we hybtidize atomic orbitals to explain the...Ch. 9 - What hybridization is required for central atoms...Ch. 9 - Describe the bonding in H2S, CH4, H2CO and HCN...Ch. 9 - What hybridization is required for central atoms...Ch. 9 - Electrons in bonding molecular orbitals are most...Ch. 9 - What are molecular orbitals? How do they compare...Ch. 9 - Explain the difference between the and MOs for...Ch. 9 - Compare Figs. 4-47 and 4-49. Why are they...Ch. 9 - Which of the following would you expect to be more...Ch. 9 - Draw the Lewis structure for HCN. Indicate the...
Ch. 9 - Which is the more correct statement: The methane...Ch. 9 - Compare and contrast the MO model with the local...Ch. 9 - What are the relationships among bond order, bond...Ch. 9 - In the hybrid orbital model, compare and contrast ...Ch. 9 - In the molecular orbital mode l, compare and...Ch. 9 - Why are d orbitals sometimes used to form hybrid...Ch. 9 - The atoms in a single bond can rotate about the...Ch. 9 - Compare and contrast bonding molecular orbitals...Ch. 9 - What modification to the molecular orbital model...Ch. 9 - Why does the molecular orbital model do a better...Ch. 9 - The three NO bonds in NO3 are all equivalent in...Ch. 9 - Use the localized electron model to describe the...Ch. 9 - Use the localized electron model to describe the...Ch. 9 - Use the localized electron model to describe the...Ch. 9 - Use the localized electron model to describe the...Ch. 9 - The space-filling models of ethane and ethanol are...Ch. 9 - The space-filling models of hydrogen cyanide and...Ch. 9 - Give the expected hybridization of the central...Ch. 9 - Give the expected hybridization of the central...Ch. 9 - Give the expected hybridization of the central...Ch. 9 - Give the expected hybridization of the central...Ch. 9 - For each of the following molecules, write the...Ch. 9 - For each of the following molecules or ions that...Ch. 9 - Prob. 31ECh. 9 - The allene molecule has the following Lewis...Ch. 9 - Indigo is the dye used in coloring blue jeans. The...Ch. 9 - Urea, a compound formed in the liver, is one of...Ch. 9 - Biacetyl and acetoin are added to margarine to...Ch. 9 - Many important compounds in the chemical industry...Ch. 9 - Two molecules used in the polymer industry are...Ch. 9 - Hot and spicy foods contain molecules that...Ch. 9 - One of the first drugs to be approved for use in...Ch. 9 - The antibiotic thiarubin-A was discovered by...Ch. 9 - Consider the following molecular orbitals formed...Ch. 9 - Sketch the molecular orbital and label its type (...Ch. 9 - Which of the following are predicted by the...Ch. 9 - Which of the following are predicted by the...Ch. 9 - Using the molecular orbital model, write electron...Ch. 9 - Consider the following electron configuration:...Ch. 9 - Using molecular orbital theory, explain why the...Ch. 9 - Using the molecular orbital model to describe the...Ch. 9 - The transport of O2 in the blood is carried out by...Ch. 9 - A Lewis structure obeying the octet rule can be...Ch. 9 - Using the molecular orbital model, write electron...Ch. 9 - Using the molecular orbital model, write electron...Ch. 9 - In which of the following diatomic molecules would...Ch. 9 - In terms of the molecular orbital model, which...Ch. 9 - Show how two 2p atomic orbitals can combine to...Ch. 9 - Show how a hydrogen 1s atomic orbital and a...Ch. 9 - Use Figs. 4-54 and 4-55 to answer the following...Ch. 9 - Acetylene (C2H2) can be produced from the reaction...Ch. 9 - Describe the bonding in NO+, NO, and NO, using...Ch. 9 - Describe the bonding in the O3 molecule and the...Ch. 9 - Describe the bonding in the CO32 ion using the...Ch. 9 - Draw the Lewis structures, predict the molecular...Ch. 9 - FClO2 and F3ClO can both gain a fluoride ion to...Ch. 9 - Two structures can be drawn for cyanuric acid: a....Ch. 9 - Give the expected hybridization for the molecular...Ch. 9 - Vitamin B6 is an organic compound whose deficiency...Ch. 9 - Aspartame is an artificial sweetener marketed...Ch. 9 - Prob. 69AECh. 9 - The three most stable oxides of carbon are carbon...Ch. 9 - Complete the following resonance structures for...Ch. 9 - Prob. 73AECh. 9 - Describe the bonding in the first excited state of...Ch. 9 - Using an MO energy-level diagram, would you expect...Ch. 9 - Show how a dxz. atomic orbital and a pz, atomic...Ch. 9 - What type of molecular orbital would result from...Ch. 9 - Consider three molecules: A, B, and C. Molecule A...Ch. 9 - Draw the Lewis structures for TeCl4, ICl5, PCl5,...Ch. 9 - A variety of chlorine oxide fluorides and related...Ch. 9 - Pelargondin is the molecule responsible for the...Ch. 9 - Complete a Lewis structure for the compound shown...Ch. 9 - Which of the following statements concerning SO2...Ch. 9 - Consider the molecular orbital electron...Ch. 9 - Place the species B2+ , B2, and B2 in order of...Ch. 9 - Consider the following computer-generated model of...Ch. 9 - Cholesterol (C27liu;O) has the following...Ch. 9 - Cyanamide (H2NCN), an important industrial...Ch. 9 - A flask containing gaseous N2 is irradiated with...Ch. 9 - Prob. 92CPCh. 9 - Values of measured bond energies may vary greatly...Ch. 9 - Use the MO model to explain the bonding in BeH2....Ch. 9 - Prob. 95CPCh. 9 - Arrange the following from lowest to highest...Ch. 9 - Use the MO model to determine which of the...Ch. 9 - Given that the ionization energy of F2 is 290...Ch. 9 - Carbon monoxide (CO) forms bonds to a variety of...Ch. 9 - Prob. 100CPCh. 9 - As the bead engineer of your starship in charge of...Ch. 9 - Determine the molecular structure and...
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