Chemistry
9th Edition
ISBN: 9781133611097
Author: Steven S. Zumdahl
Publisher: Cengage Learning
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Textbook Question
Chapter 9, Problem 12Q
The atoms in a single bond can rotate about the internuclear axis without breaking the bond. The atoms in a double and triple bond cannot rotate about the internuclear axis unless the bond is broken. Why?
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Predicting the pr
Predict the major products of the following organic reaction:
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propose synthesis
Explanation
O Conjugated Pi Systems
Deducing the reactants of a Diels-Alder reaction
Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one
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Δ
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Chapter 9 Solutions
Chemistry
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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- Diels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).arrow_forwardHELP! URGENT! PLEASE RESOND ASAP!arrow_forwardQuestion 4 Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267 First-order, k = 0.210 hour 1 First-order, k = 0.0912 hour 1 O Second-order, k = 0.590 M1 hour 1 O Zero-order, k = 0.0770 M/hour O Zero-order, k = 0.4896 M/hour O Second-order, k = 1.93 M-1-hour 1 10 ptsarrow_forward
- Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267arrow_forwardDraw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry. Ignore inorganic byproducts. OSO4 (cat) (CH3)3COOH Select to Draw ઘarrow_forwardCalculate the reaction rate for selenious acid, H2SeO3, if 0.1150 M I-1 decreases to 0.0770 M in 12.0 minutes. H2SeO3(aq) + 6I-1(aq) + 4H+1(aq) ⟶ Se(s) + 2I3-1(aq) + 3H2O(l)arrow_forward
- Problem 5-31 Which of the following objects are chiral? (a) A basketball (d) A golf club (b) A fork (c) A wine glass (e) A spiral staircase (f) A snowflake Problem 5-32 Which of the following compounds are chiral? Draw them, and label the chirality centers. (a) 2,4-Dimethylheptane (b) 5-Ethyl-3,3-dimethylheptane (c) cis-1,4-Dichlorocyclohexane Problem 5-33 Draw chiral molecules that meet the following descriptions: (a) A chloroalkane, C5H11Cl (c) An alkene, C6H12 (b) An alcohol, C6H140 (d) An alkane, C8H18 Problem 5-36 Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How H3C CH3 many chirality centers does erythronolide B have? OH Identify them. H3C -CH3 OH Erythronolide B H3C. H3C. OH OH CH3arrow_forwardPLEASE HELP! URGENT! PLEASE RESPOND!arrow_forward2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forward
- Steps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forwardSteps and explanationn please.arrow_forward
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