Chemical Principles
8th Edition
ISBN: 9781305581982
Author: Steven S. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Chapter 14, Problem 15E
Interpretation Introduction
Interpretation: The bonding in
Concept Introduction: According to LE model (Localized Electron Model), a molecule is assumed to be a collection of atoms that are bound together via sharing of electrons between the atomic orbitals.
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Chapter 14 Solutions
Chemical Principles
Ch. 14 - Prob. 1DQCh. 14 - Prob. 2DQCh. 14 - Prob. 3DQCh. 14 - Prob. 4DQCh. 14 - Prob. 5DQCh. 14 - Prob. 6DQCh. 14 - Compare and contrast the MO model with the LE...Ch. 14 - Prob. 8DQCh. 14 - Prob. 9ECh. 14 - Prob. 10E
Ch. 14 - Prob. 11ECh. 14 - Prob. 12ECh. 14 - Prob. 13ECh. 14 - Use the localized electron model to describe the...Ch. 14 - Prob. 15ECh. 14 - Use the LE model to describe the bonding in H2CO...Ch. 14 - Prob. 17ECh. 14 - The space-filling models of hydrogen cyanide and...Ch. 14 - Prob. 19ECh. 14 - Prob. 20ECh. 14 - Prob. 21ECh. 14 - Indigo is the dye used in coloring blue jeans. The...Ch. 14 - Prob. 23ECh. 14 - Prob. 24ECh. 14 - Why must all six atoms in C2H4 be in the same...Ch. 14 - The allene molecule has the following Lewis...Ch. 14 - Biacetyl and acetoin are added to margarine to...Ch. 14 - Many important compounds in the chemical industry...Ch. 14 - Prob. 29ECh. 14 - Hot and spicy foods contain molecules that...Ch. 14 - Two molecules used in the polymer industry are...Ch. 14 - Prob. 32ECh. 14 - The three most stable oxides of carbon are carbon...Ch. 14 - Prob. 34ECh. 14 - Prob. 35ECh. 14 - What are the relationships among bond order, bond...Ch. 14 - Prob. 37ECh. 14 - A Lewis structure obeying the octet rule can be...Ch. 14 - Prob. 39ECh. 14 - Why does the molecular orbital model do a better...Ch. 14 - Prob. 41ECh. 14 - Prob. 42ECh. 14 - Prob. 43ECh. 14 - In which of the following diatomic molecules would...Ch. 14 - Prob. 45ECh. 14 - Using the molecular orbital model to describe the...Ch. 14 - The transport of O2 in the blood is carried out by...Ch. 14 - Prob. 48ECh. 14 - Prob. 49ECh. 14 - Consider the following electron configuration:...Ch. 14 - Prob. 51ECh. 14 - Using an MO energy-level diagram, would you expect...Ch. 14 - Use Figs.14.45 and 14.46 to answer the following...Ch. 14 - The diatomic molecule OH exists in the gas phase....Ch. 14 - Prob. 55ECh. 14 - Describe the bonding in the O3 molecule and the...Ch. 14 - Prob. 57ECh. 14 - The space-filling model for benzoic acid is shown...Ch. 14 - Prob. 59ECh. 14 - Prob. 60ECh. 14 - The microwave spectrum of 12C16O shows that the...Ch. 14 - Prob. 62ECh. 14 - Prob. 63ECh. 14 - Prob. 64ECh. 14 - Draw the Lewis structures, predict the molecular...Ch. 14 - Prob. 66AECh. 14 - Prob. 67AECh. 14 - Prob. 68AECh. 14 - Prob. 69AECh. 14 - Prob. 70AECh. 14 - Prob. 71AECh. 14 - Prob. 72AECh. 14 - Prob. 73AECh. 14 - Vitamin B6 is an organic compound whose deficiency...Ch. 14 - Prob. 75AECh. 14 - Prob. 76AECh. 14 - Prob. 77AECh. 14 - Prob. 78AECh. 14 - Prob. 79AECh. 14 - Draw the Lewis structures for TeCl4 , ICl5 , PCl5...Ch. 14 - Prob. 81AECh. 14 - Pelargondin is the molecule responsible for the...Ch. 14 - Prob. 83AECh. 14 - Prob. 84AECh. 14 - Prob. 85AECh. 14 - Prob. 86AECh. 14 - Given that the ionization energy of F2 is...Ch. 14 - Bond energy has been defined in the text as the...Ch. 14 - a.A flask containing gaseous N2 is irradiated with...Ch. 14 - Use the MO model to determine which of the...Ch. 14 - Cholesterol (C27H46O) has the following structure:...Ch. 14 - Arrange the following from lowest to highest...Ch. 14 - Carbon monoxide (CO) forms bonds to a variety of...Ch. 14 - Prob. 94CPCh. 14 - In Exercise71 in Chapter13 , the Lewis structures...Ch. 14 - Prob. 96CPCh. 14 - Prob. 97CPCh. 14 - Prob. 98MP
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- IX) By writing the appropriate electron configurations and orbital box diagrams briefly EXPLAIN in your own words each one of the following questions: a) The bond length of the Br2 molecule is 2.28 Å, while the bond length of the compound KBr is 3.34 Å. The radius of K✶ is 1.52 Å. Determine the atomic radius in Å of the bromine atom and of the bromide ion. Br = Br b) Explain why there is a large difference in the atomic sizes or radius of the two (Br and Br). Tarrow_forwardWhen 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol.arrow_forwardWhen 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol. Which experimental number must be initialled by the Lab TA for the first run of Part 1 of the experiment? a) the heat capacity of the calorimeter b) Mass of sample c) Ti d) The molarity of the HCl e) Tfarrow_forward
- Predict products for the Following organic rxn/s by writing the structurels of the correct products. Write above the line provided" your answer D2 ①CH3(CH2) 5 CH3 + D₂ (adequate)" + 2 mited) 19 Spark Spark por every item. 4 CH 3 11 3 CH 3 (CH2) 4 C-H + CH3OH CH2 CH3 + CH3 CH2OH 0 CH3 fou + KMnDy→ C43 + 2 KMn Dy→→ C-OH ") 0 C-OH 1110 (4.) 9+3 =C CH3 + HNO 3 0 + Heat> + CH3 C-OH + Heat CH2CH3 - 3 2 + D Heat H 3 CH 3 CH₂ CH₂ C = CH + 2 H₂ → 2 2arrow_forwardWhen 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol.arrow_forwardQ6: Using acetic acid as the acid, write the balanced chemical equation for the protonation of the two bases shown (on the -NH2). Include curved arrows to show the mechanism. O₂N- O₂N. -NH2 -NH2 a) Which of the two Bronsted bases above is the stronger base? Why? b) Identify the conjugate acids and conjugate bases for the reactants. c) Identify the Lewis acids and bases in the reactions.arrow_forward
- Q5: For the two reactions below: a) Use curved electron-pushing arrows to show the mechanism for the reaction in the forward direction. Redraw the compounds to explicitly illustrate all bonds that are broken and all bonds that are formed. b) Label Bronsted acids and bases in the left side of the reactions. c) For reaction A, which anionic species is the weakest base? Which neutral compound is the stronger acid? Is the forward or reverse reaction favored? d) Label Lewis acids and bases, nucleophiles and electrophiles in the left side of the reactions. A. 용 CH3OH я хон CH3O OH B. HBr CH3ONa NaBr CH3OHarrow_forwardpotential energy Br b) Translate the Newman projection below to its wedge-and-dash drawing. F H. OH CH3 CI c) Isopentane (2-methylbutane) is a compound containing a branched carbon chain. Draw a Newman projection of six conformations about the C2-C3 bond of isopentane. On the curve of potential energy versus angle of internal rotation for isopentane, label each energy maximum and minimum with one of the conformations. 0° 。 F A B D C angle of internal rotation E F 360° (=0°) JDownlarrow_forwardQ7: Identify the functional groups in these molecules a) CH 3 b) Aspirin: HO 'N' Capsaicin HO O CH3 CH 3arrow_forward
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