
Bundle: Chemistry: An Atoms First Approach, Loose-leaf Version, 2nd + OWLv2 with Student Solutions Manual, 4 terms (24 months) Printed Access Card
2nd Edition
ISBN: 9781337086431
Author: Steven S. Zumdahl, Susan A. Zumdahl
Publisher: Cengage Learning
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Textbook Question
Chapter 4, Problem 29E
State whether or not each of the following has a permanent dipole moment.
a.
b.
c.
d.
e.
f.
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Consider the "C NMR spectrum below.
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The spectrum belongs to which one of the following constitutional isomers of the compound C,H12? Select the single best answer.
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The structure of compound 1,3,5-trimethylbenzene (mesitylene) is given below.
How many signals would you expect to find in the 'H NMR spectrum of 1,3,5-trimethylbenzene (mesitylene)?
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1
How many signals do you expect in the 'H NMR spectrum for this molecule?
CI CI
Cl
Write the answer in the table below.
Also, in each of the drawing areas below is a copy of the molecule, with H atoms shown. In each copy, one of the H atoms is highlighted red. Highlight in red all
other H atoms that would contribute to the same signal as the H already highlighted red.
Note for advanced students: Remember, a multiplet is considered one signal in the 'H NMR spectrum.
1
Number of signals in the 'H NMR spectrum.
☐
For the molecule in the top drawing area, highlight in red any other H atoms that will contribute to the same
signal as the H atom already highlighted red.
If no other H atoms will contribute, check the box at right.
No additional H atoms to highlight in
top molecule
For the molecule in the bottom drawing area, highlight in red any other H atoms that will contribute to the
same signal as the H atom already highlighted red.
If no other H atoms will contribute, check the box at…
Chapter 4 Solutions
Bundle: Chemistry: An Atoms First Approach, Loose-leaf Version, 2nd + OWLv2 with Student Solutions Manual, 4 terms (24 months) Printed Access Card
Ch. 4 - Explain the main postulate of the VSEPR model....Ch. 4 - Explain why CF4 and Xef4 are nonpolar compounds...Ch. 4 - Consider the following compounds: CO2, SO2, KrF2,...Ch. 4 - Prob. 4RQCh. 4 - What hybridization is required for central atoms...Ch. 4 - Prob. 6RQCh. 4 - Prob. 7RQCh. 4 - What are molecular orbitals? How do they compare...Ch. 4 - Explain the difference between the and MOs for...Ch. 4 - Prob. 3ALQ
Ch. 4 - Which of the following would you expect to be more...Ch. 4 - Arrange the following molecules from most to least...Ch. 4 - Which is the more correct statement: The methane...Ch. 4 - Prob. 7ALQCh. 4 - Prob. 8ALQCh. 4 - Which of the following statements is/are true?...Ch. 4 - Give one example of a compound having a linear...Ch. 4 - In the hybrid orbital model, compare and contrast ...Ch. 4 - Prob. 13QCh. 4 - Prob. 14QCh. 4 - Prob. 15QCh. 4 - Prob. 16QCh. 4 - Compare and contrast bonding molecular orbitals...Ch. 4 - Prob. 18QCh. 4 - Why does the molecular orbital model do a better...Ch. 4 - The three NO bonds in NO3 are all equivalent in...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure and bond angles...Ch. 4 - Prob. 24ECh. 4 - Prob. 25ECh. 4 - Two variations of the octahedral geometry (see...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - State whether or not each of the following has a...Ch. 4 - The following electrostatic potential diagrams...Ch. 4 - Which of the molecules in Exercises 21 and 22 have...Ch. 4 - Which of the molecules in Exercises 27 and 28 have...Ch. 4 - Write Lewis structures and predict the molecular...Ch. 4 - Write Lewis structures and predict whether each of...Ch. 4 - Consider the following Lewis structure where E is...Ch. 4 - Consider the following Lewis structure where E is...Ch. 4 - The molecules BF3, CF4, CO2, PF5, and SF6 are all...Ch. 4 - Two different compounds have the formula XeF2Cl2....Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - The space-filling models of ethane and ethanol are...Ch. 4 - The space-filling models of hydrogen cyanide and...Ch. 4 - Prob. 45ECh. 4 - Prob. 46ECh. 4 - Prob. 47ECh. 4 - Give the expected hybridization of the central...Ch. 4 - For each of the following molecules, write the...Ch. 4 - For each of the following molecules or ions that...Ch. 4 - Prob. 51ECh. 4 - The allene molecule has the following Lewis...Ch. 4 - Indigo is the dye used in coloring blue jeans. The...Ch. 4 - Prob. 54ECh. 4 - Prob. 55ECh. 4 - Many important compounds in the chemical industry...Ch. 4 - Two molecules used in the polymer industry are...Ch. 4 - Hot and spicy foods contain molecules that...Ch. 4 - One of the first drugs to be approved for use in...Ch. 4 - The antibiotic thiarubin-A was discovered by...Ch. 4 - Prob. 61ECh. 4 - Sketch the molecular orbital and label its type (...Ch. 4 - Prob. 63ECh. 4 - Which of the following are predicted by the...Ch. 4 - Prob. 65ECh. 4 - Prob. 66ECh. 4 - Prob. 67ECh. 4 - Using the molecular orbital model to describe the...Ch. 4 - Prob. 69ECh. 4 - A Lewis structure obeying the octet rule can be...Ch. 4 - Using the molecular orbital model, write electron...Ch. 4 - Using the molecular orbital model, write electron...Ch. 4 - In which of the following diatomic molecules would...Ch. 4 - In terms of the molecular orbital model, which...Ch. 4 - Prob. 75ECh. 4 - Show how a hydrogen 1s atomic orbital and a...Ch. 4 - Use Figs. 4-54 and 4-55 to answer the following...Ch. 4 - The diatomic molecule OH exists in the gas phase....Ch. 4 - Prob. 79ECh. 4 - Describe the bonding in NO+, NO, and NO, using...Ch. 4 - Describe the bonding in the O3 molecule and the...Ch. 4 - Prob. 82ECh. 4 - Prob. 83AECh. 4 - Vitamin B6 is an organic compound whose deficiency...Ch. 4 - Two structures can be drawn for cyanuric acid: a....Ch. 4 - Prob. 86AECh. 4 - What do each of the following sets of...Ch. 4 - Aspartame is an artificial sweetener marketed...Ch. 4 - Prob. 89AECh. 4 - The three most stable oxides of carbon are carbon...Ch. 4 - Prob. 91AECh. 4 - Which of the following molecules have net dipole...Ch. 4 - The strucrure of TeF5 is Draw a complete Lewis...Ch. 4 - Complete the following resonance structures for...Ch. 4 - Prob. 95AECh. 4 - Describe the bonding in the first excited state of...Ch. 4 - Using an MO energy-level diagram, would you expect...Ch. 4 - Show how a dxz. atomic orbital and a pz, atomic...Ch. 4 - What type of molecular orbital would result from...Ch. 4 - Consider three molecules: A, B, and C. Molecule A...Ch. 4 - Prob. 101CWPCh. 4 - Predict the molecular structure, bond angles, and...Ch. 4 - Draw the Lewis structures for SO2, PCl3, NNO, COS,...Ch. 4 - Draw the Lewis structures for TeCl4, ICl5, PCl5,...Ch. 4 - A variety of chlorine oxide fluorides and related...Ch. 4 - Pelargondin is the molecule responsible for the...Ch. 4 - Complete a Lewis structure for the compound shown...Ch. 4 - Prob. 108CWPCh. 4 - Consider the molecular orbital electron...Ch. 4 - Place the species B2+ , B2, and B2 in order of...Ch. 4 - The compound NF3 is quite stable, but NCl3 is very...Ch. 4 - Predict the molecular structure for each of the...Ch. 4 - Prob. 113CPCh. 4 - Cholesterol (C27liu;O) has the following...Ch. 4 - Cyanamide (H2NCN), an important industrial...Ch. 4 - As compared with CO and O2, CS and S2 are very...Ch. 4 - Prob. 117CPCh. 4 - Use the MO model to explain the bonding in BeH2....Ch. 4 - Prob. 119CPCh. 4 - Arrange the following from lowest to highest...Ch. 4 - Prob. 121CPCh. 4 - Prob. 122CPCh. 4 - Carbon monoxide (CO) forms bonds to a variety of...Ch. 4 - The space-filling model for benzoic acid, a food...Ch. 4 - As the bead engineer of your starship in charge of...Ch. 4 - A flask containing gaseous N2 is irradiated with...Ch. 4 - Determine the molecular structure and...
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- wrtie the balanced equation and find the E° when the following half- reactions are combined Zn2+(aq) + 2e---> Zn(s) E°= -0.763V Ag+(aq) + e---> Ag (s) E°=+0.799Varrow_forwardConsider this molecule: How many H atoms are in this molecule? How many different signals could be found in its 'H NMR spectrum? Note: A multiplet is considered one signal. ☐arrow_forwardStudy this 'H NMR spectrum, and then answer the questions about it in the table below. Check 1.0- 0.5- 0.0 10.0 9.0 8.0 7.0 6.0 5.0 4.0 3.0 2.0 1.0 0.0 What unit symbol should be written on the horizontal axis? What is the chemical shift & of the doublet? If there is no doublet, just check the box instead. Give your answer to 2 significant digits. What is the chemical shift of the signal immediately upfield of the doublet? If there is no doublet, or no signal upfield of it, check the box instead. What is the chemical shift & of the least deshielded proton? If you can't tell without more information, check the box instead. 血 8 = ☐ There is no doublet. 8 = ☐ No such signal. 8 = 0 Need more information.arrow_forward
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- Using reaction free energy to predict equilibrium composition Consider the following equilibrium: 2NO2 (g) = N2O4(g) AGº = -5.4 kJ Now suppose a reaction vessel is filled with 4.53 atm of dinitrogen tetroxide (N2O4) at 279. °C. Answer the following questions about this system: Under these conditions, will the pressure of N2O4 tend to rise or fall? Is it possible to reverse this tendency by adding NO2? In other words, if you said the pressure of N2O4 will tend to rise, can that be changed to a tendency to fall by adding NO2? Similarly, if you said the pressure of N2O4 will tend to fall, can that be changed to a tendency to '2' rise by adding NO2? If you said the tendency can be reversed in the second question, calculate the minimum pressure of NO 2 needed to reverse it. Round your answer to 2 significant digits. 00 rise ☐ x10 fall yes no ☐ atm G Ar 1arrow_forwardWhy do we analyse salt?arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. H H CH3OH, H+ H Select to Add Arrows H° 0:0 'H + Q HH ■ Select to Add Arrows CH3OH, H* H. H CH3OH, H+ HH ■ Select to Add Arrows i Please select a drawing or reagent from the question areaarrow_forward
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