OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
5th Edition
ISBN: 9781285460420
Author: John W. Moore; Conrad L. Stanitski
Publisher: Cengage Learning US
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Textbook Question
Chapter 7, Problem 5QRT
If you have three electron regions around a central atom, how can you have a triangular planar molecule? An angular molecule? What bond angles are predicted in each case?
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What are the angles a and b in the actual molecule of which this is a Lewis structure?
H H
H
C
H
a
a =
C
b = ⁰
C
H
Note for advanced students: give the ideal angles, and don't worry about small differences from the ideal that might be caused by the fact that
different electron groups may have slightly different sizes.
H
X
Use VSEPR to predict the geometry (including bond angles) about each interior atom of methyl azide (CH3N3) and draw the molecule. Would you expect the bond angle between the two interior nitrogen atoms to be the same or different? Would you expect the two nitrogen–nitrogen bond lengths to be the same or different?
Use VSEPR theory to predict the geometry (including bond angles) about each interior atom of methyl azide (CH3N3), and make a sketch of the molecule. Would you expect the bond angle between the two interior nitrogen atoms to be the same or different? Would you expect the two nitrogen–nitrogen bond lengths to be the same or different?
Chapter 7 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
Ch. 7.2 - Identify the electron-region geometry, the...Ch. 7.2 - Based on the discussion so far, identify a...Ch. 7.2 - Prob. 7.2PSPCh. 7.2 - Determine the electron-region geometry and the...Ch. 7.2 - Prob. 7.2CECh. 7.2 - Prob. 7.3ECh. 7.2 - Prob. 7.4PSPCh. 7.4 - Using hybridization and sigma and pi bonding,...Ch. 7.4 - Prob. 7.4CECh. 7.5 - Decide whether each molecule is polar and, if so,...
Ch. 7.5 - Prob. 7.5ECh. 7.6 - Prob. 7.8PSPCh. 7.6 - Prob. 7.7CECh. 7.6 - Prob. 7.9PSPCh. 7.7 - Prob. 7.8CECh. 7.7 - Prob. 7.9CECh. 7 - Write the Lewis structures and give the...Ch. 7 - The structural formula for the open-chain form of...Ch. 7 - Describe the VSEPR model. How is the model used to...Ch. 7 - What is the difference between the electron-region...Ch. 7 - Prob. 3QRTCh. 7 - Prob. 4QRTCh. 7 - If you have three electron regions around a...Ch. 7 - Prob. 6QRTCh. 7 - Prob. 7QRTCh. 7 - Prob. 8QRTCh. 7 - Prob. 9QRTCh. 7 - Prob. 10QRTCh. 7 - Prob. 11QRTCh. 7 - Prob. 12QRTCh. 7 - Prob. 13QRTCh. 7 - Prob. 14QRTCh. 7 - Prob. 15QRTCh. 7 - Prob. 16QRTCh. 7 - Write Lewis structures for XeOF2 and ClOF3. Use...Ch. 7 - Write Lewis structures for HCP and [IOF4]. Use...Ch. 7 - Prob. 19QRTCh. 7 - Prob. 20QRTCh. 7 - Explain why (I3)+ is bent, but (I3) is linear.Ch. 7 - Prob. 22QRTCh. 7 - Prob. 23QRTCh. 7 - Give approximate values for the indicated bond...Ch. 7 - Give approximate values for the indicated bond...Ch. 7 - Prob. 26QRTCh. 7 - Compare the FClF angles in ClF2+ and ClF2. From...Ch. 7 - Prob. 28QRTCh. 7 - Prob. 29QRTCh. 7 - Prob. 30QRTCh. 7 - Prob. 31QRTCh. 7 - Describe the geometry and hybridization of carbon...Ch. 7 - Describe the geometry and hybridization for each C...Ch. 7 - Describe the hybridization around the central atom...Ch. 7 - The hybridization of the two carbon atoms differs...Ch. 7 - The hybridization of the two nitrogen atoms...Ch. 7 - Identify the type of hybridization, approximate...Ch. 7 - Prob. 38QRTCh. 7 - Prob. 39QRTCh. 7 - Prob. 40QRTCh. 7 - Prob. 41QRTCh. 7 - Methylcyanoacrylate is the active ingredient in...Ch. 7 - Prob. 43QRTCh. 7 - Prob. 44QRTCh. 7 - Prob. 45QRTCh. 7 - Prob. 46QRTCh. 7 - Which of these molecules has a net dipole moment?...Ch. 7 - Prob. 48QRTCh. 7 - Use molecular structures and noncovalent...Ch. 7 - Prob. 50QRTCh. 7 - Explain why water “beads up” on a freshly waxed...Ch. 7 - Explain why water will not remove tar from your...Ch. 7 - Prob. 53QRTCh. 7 - Prob. 54QRTCh. 7 - Prob. 55QRTCh. 7 - Prob. 56QRTCh. 7 - The structural formula for vitamin C is Give a...Ch. 7 - Prob. 58QRTCh. 7 - Prob. 59QRTCh. 7 - Prob. 60QRTCh. 7 - Prob. 61QRTCh. 7 - Prob. 62QRTCh. 7 - Prob. 63QRTCh. 7 - Prob. 64QRTCh. 7 - Prob. 65QRTCh. 7 - Prob. 66QRTCh. 7 - Methylcyanoacrylate is the active ingredient in...Ch. 7 - Prob. 68QRTCh. 7 - Prob. 69QRTCh. 7 - Use Lewis structures and VSEPR theory to predict...Ch. 7 - In addition to CO, CO2, and C3O2, there is another...Ch. 7 - Prob. 72QRTCh. 7 - Prob. 73QRTCh. 7 - Prob. 74QRTCh. 7 - Prob. 75QRTCh. 7 - In the gas phase, positive and negative ions form...Ch. 7 - Prob. 77QRTCh. 7 - Prob. 78QRTCh. 7 - Prob. 79QRTCh. 7 - Prob. 80QRTCh. 7 - Prob. 81QRTCh. 7 - Prob. 82QRTCh. 7 - Prob. 83QRTCh. 7 - Prob. 84QRTCh. 7 - Prob. 85QRTCh. 7 - Prob. 86QRTCh. 7 - Prob. 87QRTCh. 7 - Prob. 88QRTCh. 7 - Prob. 89QRTCh. 7 - Prob. 90QRTCh. 7 - Prob. 91QRTCh. 7 - Prob. 92QRTCh. 7 - Prob. 93QRTCh. 7 - Prob. 94QRTCh. 7 - Which of these are examples of hydrogen bonding?Ch. 7 - Prob. 96QRTCh. 7 - Prob. 97QRTCh. 7 - Prob. 98QRTCh. 7 - Halothane, which had been used as an anesthetic,...Ch. 7 - Ketene, C2H2O, is a reactant for synthesizing...Ch. 7 - Gamma hydroxybutyric acid, GHB, infamous as a date...Ch. 7 - There are two compounds with the molecular formula...Ch. 7 - Piperine, the active ingredient in black pepper,...Ch. 7 - Prob. 105QRTCh. 7 - Two compounds have the molecular formula N3H3. One...Ch. 7 - Prob. 108QRTCh. 7 - Prob. 109QRTCh. 7 - Prob. 110QRTCh. 7 - Prob. 111QRTCh. 7 - Prob. 7.ACPCh. 7 - Prob. 7.BCPCh. 7 - Prob. 7.CCPCh. 7 - Prob. 7.DCP
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- In each of the following molecules, a central atom is surrounded by a total of three atoms or unshared electron pairs: SnCl2, BCl3, SO2. In which of these molecules would you expect the bond angle to be less than 120? Explain your reasoning.arrow_forwardConsider the following molecules: SiH4, PH3, H2S. In each case, a central atom is surrounded by four electron pairs. In which of these molecules would you expect the bond angle to be less than 109.5? Explain your reasoning.arrow_forwardUse the VSEPR model to predict the bond angles around each central atom in the following Lewis structures (benzene rings are frequently pictured as hexagons, without the letter for the carbon atom at each vertex). Note that the drawings do not necessarily depict the bond angles correctly.arrow_forward
- 7.59 What type of hybrid orbital is generated by combining the valence s orbital and all three valence p orbitals of an atom? How many hybrid orbitals result?arrow_forwardAn objectionable component of smog is acetyl peroxide, which has the following skeleton structure. (a) Draw the Lewis structure of this compound. (b) Write the bond angles indicated by the numbered angles.arrow_forwardWhich statement best captures the fundamental idea behind VSEPR theory? Explain what is wrong with the statements you do not choose. a. The angle between two or more bonds is determined primarily by the repulsions between the electrons within those bonds and other (lone pair) electrons on the central atom of a molecule. Each of these electron groups (bonding electrons or lone pair electrons) lowers its potential energy by maximizing its separation from other electron groups, thus determining the geometry of the molecule. b. The angle between two or more bonds is determined primarily by the repulsions between the electrons within those bonds. Each of these bonding electrons lowers its potential energy by maximizing its separation from other electron groups, thus determining the geometry of the molecule. c. The geometry of a molecule is determined by the shapes of the overlapping orbitals that form the chemical bonds. Therefore, to determine the geometry of a molecule, you must determine…arrow_forward
- How does adding an atom affect the position and angles of existing atoms or lone pairs? How does adding a lone pair affect the position and angles of existing atoms and lone pairs? Is the effect of adding bonded atoms and lone pairs to the central similar? Explain your answer. Describe what is meant by the "Steric #". Explain the difference between the terms "Electron Geometry" and "Molecule Geometry". How does changing a bond to a double or triple bond affect the shape of the molecules? List the molecules in Part III where the real bond angles differ from the theoretical model values. Why do you think the values differ?arrow_forward) Bean hexene is an odor compound used in cosmetics and cleaners. It is also known as leguminal. Its formula is: CH3CH2CHCHCH2CH2OCHCH2CH3 | OCH3 Please draw a Lewis structure for this compound with CORRECT GEOMETRY (use dashes and wedges!) Label all pi bonds in the molecule (if there are any) Indicate the bond angles for the red highlighted section of the molecule. (hint: you may want to keep the main carbon chain in-plane with the page for clarity) For this question, you don’t need to draw out the orbitals.arrow_forwardWhat effect does the presence of lone-pair electrons have on the bond angles in a molecule?arrow_forward
- The Lewis structure for SF6 is shown below. This sulfur S atom in this molecule has an expanded octet, and you are not expected to be familiar with the specific electron geometry and molecular geometry for expanded octets. Still, we can make some predictions with the knowledge that we have. Would you predict the electron geometry and molecular geometry for SF6 to be the same or to differ? Please briefly explain your answer.arrow_forwardPredict the geometry and bond angles around atom A for molecules with the general formulas AB3 and AB2E, where B represents another atom and E represents an electron pair.arrow_forwardWhat are the angles a and b in the actual molecule of which this is a Lewis structure? H- H a-0° b = 1⁰ C H a b H Note for advanced students: give the ideal angles, and don't worry about small differences from the ideal that might be caused by the fact that different electron groups may have slightly different sizes. X Sarrow_forward
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