LCPO CHEMISTRY W/MODIFIED MASTERING
8th Edition
ISBN: 9780135214756
Author: Robinson
Publisher: PEARSON
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Chapter 8, Problem 8.109SP
Make a sketch showing the location and geometry of the porbitals in the ally location. Describe the bonding in this cation using a localized valence bond model for
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Chapter 8 Solutions
LCPO CHEMISTRY W/MODIFIED MASTERING
Ch. 8 - Prob. 8.1PCh. 8 - What is the number and geometric arrangement of...Ch. 8 - PRACTICE 8.3 Acetic acid, CH3CO2H , is the main...Ch. 8 - APPLY 8.4 Benzene, C6H6 , is a cyclic molecule in...Ch. 8 - PRACTICE 8.5 Identify the orbitals that overlap to...Ch. 8 - APPLY 8.6 Describe the bonding in propane, C3H8 ,...Ch. 8 - PRACTICE 8.7 Describe the hybridization of the...Ch. 8 - Describe the hybridization of each carbon atom in...Ch. 8 - Which orbitals overlap to form the sigma and pi...Ch. 8 - APPLY 8.10 Describe the hybridization of the...
Ch. 8 - Prob. 8.11PCh. 8 - Conceptual APPLY 8.12 Match the following...Ch. 8 - Prob. 8.13PCh. 8 - Prob. 8.14ACh. 8 - Prob. 8.15PCh. 8 - Prob. 8.16ACh. 8 - Prob. 8.17ACh. 8 - Prob. 8.18ACh. 8 - The B2 molecule has a MO diagram similar to that...Ch. 8 - Prob. 8.20ACh. 8 - PRACTICE 8.23 Draw two resonance structures for...Ch. 8 - APPLY 8.24 Draw two resonance structures for the...Ch. 8 - Prob. 8.23PCh. 8 - Prob. 8.24PCh. 8 - Caffeine is the most widely used stimulant...Ch. 8 - Prob. 8.26PCh. 8 - What is the geometry around the central atom in...Ch. 8 - What is the geometry around the central atom in...Ch. 8 - Three of the following molecular models have a...Ch. 8 - Identify each of the following sets of hybrid...Ch. 8 - The VSEPR model is a simple predictive tool that...Ch. 8 - The following ball-and-stick molecular model is a...Ch. 8 - The following ball-and-stick molecular model is a...Ch. 8 - Prob. 8.34CPCh. 8 - The dipole moment of methanol is =1.70D . Use...Ch. 8 - Methylarnine, CH3NH2 , is responsible for the odor...Ch. 8 - Prob. 8.37CPCh. 8 - Prob. 8.38SPCh. 8 - What shape do you expect for molecules that meet...Ch. 8 - How many charge clouds are there around the...Ch. 8 - Prob. 8.41SPCh. 8 - What shape do you expect for each of the following...Ch. 8 - What shape do you expect for each of the following...Ch. 8 - What shape do you expect for each of the following...Ch. 8 - Prob. 8.45SPCh. 8 - Prob. 8.46SPCh. 8 - What shape do you expect for each of the following...Ch. 8 - What bond angles do you expect for each of the...Ch. 8 - What bond angles do you expect for each of the...Ch. 8 - Acrylonitrile is used as the starting material for...Ch. 8 - Predict values for all bond angles in dimethyl...Ch. 8 - Oceanographers study the mixing of water masses by...Ch. 8 - A potential replacement for the chlorofluorocarbon...Ch. 8 - Explain why cyclohexane, a substance that contains...Ch. 8 - Like cyclohexane (Problem 8.54), benzene also...Ch. 8 - Use VSEPR theory to answer the following...Ch. 8 - Draw an electron-dot structure for each of the...Ch. 8 - What is the difference in spatial distribution...Ch. 8 - The average CC bond dissociation energy (D) is 350...Ch. 8 - What hybridization do you expect for atoms that...Ch. 8 - What spatial arrangement of charge clouds...Ch. 8 - What hybridization would you expect for the...Ch. 8 - What hybridization would you expect for the...Ch. 8 - Oxaloacetic acid is an intermediate involved in...Ch. 8 - The atoms in the amino acid glycine are connected...Ch. 8 - Describe the hybridization of the carbon atom in...Ch. 8 - Describe the hybridization of each carbon atom in...Ch. 8 - Bupropion, marketed as Wellbutr in, is a heavily...Ch. 8 - Efavirenz, marketed as Sustiva, is a medication...Ch. 8 - What is the hybridization of the B and N atoms in...Ch. 8 - Prob. 8.71SPCh. 8 - Aspirin has the following connections among atoms....Ch. 8 - The cation [HCNXeF]+ is entirely linear. Draw an...Ch. 8 - Acrylonitrile (C3H3N) is a molecule that is...Ch. 8 - The odor of cinnamon oil is due to cinnamaldehyde,...Ch. 8 - The following molecular model is a representation...Ch. 8 - Prob. 8.77SPCh. 8 - Which of the following substances would you expect...Ch. 8 - Which of the following substances would you expect...Ch. 8 - Why is the dipole moment of SO2 1.63 D hut that of...Ch. 8 - Prob. 8.81SPCh. 8 - The class of ions PtX42 , where X is a halogen,...Ch. 8 - Prob. 8.83SPCh. 8 - Prob. 8.84SPCh. 8 - Prob. 8.85SPCh. 8 - Prob. 8.86SPCh. 8 - Prob. 8.87SPCh. 8 - What are the most important kinds of...Ch. 8 - Of the substances Xe, CH3Cl , and HF which has:...Ch. 8 - Methanol (CH3OH;bp=65C) boils nearly 230 °C higher...Ch. 8 - Prob. 8.91SPCh. 8 - Prob. 8.92SPCh. 8 - Prob. 8.93SPCh. 8 - A liquid sample contains methylamine (CH3NH2)...Ch. 8 - Prob. 8.95SPCh. 8 - What is the difference in spatial distribution...Ch. 8 - Prob. 8.97SPCh. 8 - Use the MO energy diagram in Figure 8.22b to...Ch. 8 - Use the MO energy diagram in Figure 8.22 a to...Ch. 8 - The C2 molecule can be represented by an MO...Ch. 8 - Prob. 8.101SPCh. 8 - Prob. 8.102SPCh. 8 - Prob. 8.103SPCh. 8 - Draw a molecular orbital energy diagram for Li2 ....Ch. 8 - Calcium carbide, CaC2 , reacts with water to...Ch. 8 - At high temperatures, sulfur vapor is...Ch. 8 - Carbon monoxide is produced by incomplete...Ch. 8 - Make a sketch showing the location and geometry of...Ch. 8 - Make a sketch showing the location and geometry of...Ch. 8 - Prob. 8.110MPCh. 8 - Prob. 8.111MPCh. 8 - Prob. 8.112MPCh. 8 - Prob. 8.113MPCh. 8 - Just as individual bonds in a molecule are often...Ch. 8 - Cyclooctatetraenedian ion, C8H82 , is an organic...
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- • explain how hybridization reconciles observed molecular shapes with the orbital overlap model.arrow_forwardUse valence bond theory to describe the bonding in methylamine. CH3NH2.arrow_forwardIf 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?arrow_forward
- It is possible to write a simple Lewis structure for the SO42- ion, involving only single bonds, which follows the octet rule. However, Linus Pauling and others have suggested an alternative structure, involving double bonds, in which the sulfur atom is surrounded by six electron pairs. (a) Draw the two Lewis structures. (b) What geometries are predicted for the two structures? (c) What is the hybridization of sulfur in each case? (d) What are the formal charges of the atoms in the two structures?arrow_forwardPredict the valence electron molecular orbital configurations for the following, and state whether they will be stable or unstable ions. (a) Na,2+ (b) Mg,2 (c) AI,2 (d) Si,2 (e) p2+ (f) s,2 (g) F,2 (h) Ar,2 40. Predict the valence electron molecular orbital configurations for the following, and state whether they will be stable or unstable ions. (a) Na22+ (b) Mg22+ (c) Al22+ (d) Si22+ (e) P22+ (f) S22+ (g) F22+ (h) Ar22+arrow_forwardWhat is the valence bond description for H2O, HNNH, and ClF3?arrow_forward
- Draw Lewis structure for OPF, (P is the central atom). Write down all possible resonance structures, including formal charges. Draw the geometry of the ion. Indicate the hybridization of the central atom and type of orbitals involved in x bonding on both bonded atoms.arrow_forwardUse the molecular orbital model to fully describe the bonding in O2+, O2, O2-, and O22-.Determine which of the following statements are true and which are false. True or false? : Bond length increases with increasing bond order while bond energy decreases.The number of unpaired electrons in O2- and O2 is, respectively, 1 and 2. The electron configuration of O2 is (σ2s)2(σ2s*)2(σ2p)2(π2p)4(π2p*)1. The electron configuration of O2- is (σ2s)2(σ2s*)2(σ2p)2(π2p)4(π2p*)3. The bond order in O2- and O22- is, respectively, 2.5 and 1. The bond lengths increase in the order: O22- < O2- < O2 < O2+.arrow_forwardStudy the following sketch of a molecular orbital (MO) in a homonuclear diatomic molecule. This MO was formed by combining one 2p atomic orbital from atom. The dark dots in this sketch are the nuclei. Now use the sketch to complete the table below. Write the symbol for this MO. Is this a bonding or antibonding MO? What is the energy of this MO, compared to the energy of a 2p orbital on one of the separate 0 Obonding antibonding O higher Olower the same not enough information to decide D 8 70 % 9arrow_forward
- In VSEPR theory, which uses the Lewis model to determine molecular geometry, the trend of decreasing bond angles in CH4, NH3, and H2O is accounted for by the greater repulsion of lone pair electrons compared to bonding pair electrons. How would this trend be accounted for in valence bond theory?arrow_forwardThe concept of valence-shell electron-pair repulsion (VSEPR) is presented in introductory organic chemistry as a way to predict molecular geometries. The idea be- hind VSEPR is that areas of electron density repel each other so that the geometry of bonds and/or lone pairs of electrons around any one atom places these areas as far apart as possible. For four areas of electron density, a tetrahedral geometry is predicted. For three areas of electron density, a trigonal planar geometry is predicted. Two areas of electron density lead to a linear geometry. VSEPR is simply a predictive tool, but in some cases, it gives an incorrect prediction. In these instances, additional insights into bonding are necessary, such as resonance. Interestingly, several important situations are critical to biochemistry where VSEPR breaks down. Two examples are shown here. :O: CH3 H,N H3N CH3 H :0: :0: Histidine The circled nitrogen atoms are predicted by VSEPR to be tetrahedral in geometry because each…arrow_forwarddraw a Valence Bond description of bonding in the molecule, N2H2. Be sure to indicate the appropriate hybridization scheme on the nitrogen and carbon atoms, label each bonding interaction as either sigma (σ) or pi (π), and don’t neglect any lone pairs.arrow_forward
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