Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Textbook Question
Chapter 1.17, Problem 1.16P
- a. Predict the hybridization of the oxygen atom in water, H2O. Draw a picture of its three-dimensional structure, and explain why its bond angle is 104.5°.
- b. The electrostatic potential maps for ammonia and water are shown here The structure of ammonia is shown within its EPM Note how the lone pair creates a region of high electron potential (red), and the hydrogens are in regions of low electron potential (blue) Show how your three-dimensional structure of water corresponds with its EPM.
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Consider the reaction BF3 + NH3 -> F3B-NH3
(a) Describe the changes in hybridization of the B and N atoms as a result of this reaction.
(b) Describe the shapes of all the reactant molecules with their bond angles.
(c) Draw the overall shape of the product molecule and identify the bond angles around B and N atoms.
(d) What is the name of the bond between B and N.
(e)Describe the bonding orbitals that make the B and F, B and N & N and H bonds in the product molecule.
Chapter 1 Solutions
Organic Chemistry (9th Edition)
Ch. 1.2C - a. Nitrogen has relatively stable isotopes...Ch. 1.4 - Draw Lewis structures for the following compounds....Ch. 1.5 - Write Lewis structures for the following molecular...Ch. 1.5 - Circle any lone pairs (pairs of nonbonding...Ch. 1.6 - Use electronegativities to predict the direction...Ch. 1.8 - Prob. 1.6PCh. 1.9B - Draw the important resonance forms for the...Ch. 1.9B - Prob. 1.8PCh. 1.9B - Prob. 1.9PCh. 1.9B - Use resonance structures to identify the areas of...
Ch. 1.10A - Draw complete Lewis structures for the following...Ch. 1.10B - Give Lewis structures corresponding to the...Ch. 1.10B - Prob. 1.13PCh. 1.11 - Compute the empirical and molecular formulas for...Ch. 1.16 - a. Use your molecular models to make ethane, and...Ch. 1.17 - a. Predict the hybridization of the oxygen atom in...Ch. 1.17 - Predict the hybridization geometry and bond angles...Ch. 1.17 - Predict the hybridization, geometry, and bond...Ch. 1.17 - Prob. 1.19PCh. 1.17 - Allene, CH2=C=CH2, has the structure shown below...Ch. 1.17 - 1. Draw the important resonance forms for each...Ch. 1.18B - Prob. 1.22PCh. 1.18B - Two compounds with the formula CH3CH=NCH3 are...Ch. 1.19B - Prob. 1.24PCh. 1.19B - Give the relationship between the following pairs...Ch. 1 - a. Draw the resonance forms for SO2 (bonded OSO)....Ch. 1 - Name the element that corresponds to each...Ch. 1 - Prob. 1.28SPCh. 1 - For each compound, state whether its bonding is...Ch. 1 - a. Both PCl3 and PCl5 are stable compounds Draw...Ch. 1 - Draw a Lewis structure for each species a. N2H4 b....Ch. 1 - Prob. 1.32SPCh. 1 - Prob. 1.33SPCh. 1 - Draw Lewis structures for a. two compounds of...Ch. 1 - Prob. 1.35SPCh. 1 - Some of the following molecular formulas...Ch. 1 - Prob. 1.37SPCh. 1 - Give the molecular formula of each compound shown...Ch. 1 - 1. From what you remember of electronegativities,...Ch. 1 - For each of the following structures, 1. Draw a...Ch. 1 - Prob. 1.41SPCh. 1 - Prob. 1.42SPCh. 1 - Prob. 1.43SPCh. 1 - Prob. 1.44SPCh. 1 - For each pair of ions, determine which on is more...Ch. 1 - Use resonance structures to identify the areas of...Ch. 1 - Prob. 1.47SPCh. 1 - In 1934, Edward A. Doisy of Washington University...Ch. 1 - If the carbon atom in CH2Cl2 were fat. there would...Ch. 1 - Cyclopropane (C3H6, a three-membered ring) is more...Ch. 1 - Prob. 1.51SPCh. 1 - Prob. 1.52SPCh. 1 - In most amines, the nitrogen atom is sp3...Ch. 1 - Predict the hybridization and geometry of the...Ch. 1 - Draw orbital pictures of the pi bonding in the...Ch. 1 - Prob. 1.56SPCh. 1 - Prob. 1.57SPCh. 1 - Which of the following compounds show cis-trans...Ch. 1 - Give the relationships between the following pairs...Ch. 1 - Dimethyl sulfoxide (DMSO) has been used as an...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Consider the following molecular orbitals formed from the combination of two hydrogen 1s orbitals: a. Which is the bonding molecular orbital and which is the antibonding molecular orbital? Explain how you can tell by looking at their shapes. b. Which of the two molecular orbitals is lower in energy? Why is this true?arrow_forwardIdentify any carbon atoms that change hybridization and the change in hybridization during the reactions in Exercise 20.26.arrow_forwardConsider the bonding in nitrate ion, NO3. First draw resonance formulas of this ion. Now describe the bonding of this ion in terms of molecular orbitals. (Refer to the delocalized bonding of the ozone molecule described in the text.) Suppose each atom uses sp2 hybrid orbitals. How many molecular orbitals can you form from the 2p orbitals that remain on these atoms? How many of these orbitals will be occupied?arrow_forward
- The nitrosyl ion. NO+, has an interesting chemistry. Assume the molecular orbital diagram shown in Figure 9.16 applies to NO+. (a) Is NO+ diamagnetic or paramagnetic? If paramagnetic, how many unpaired electrons does it have? (b) What is the highest-energy molecular orbital (HOMO) occupied by electrons? (c) What is the nitrogen-oxygen bond order? (d) Is the NO bond in NO stronger or weaker than the bond in NO?arrow_forwardA model of the organic compound allene is shown below. (a) Explain why the allene molecule is not flat. That is. explain why the CH2 groups at opposite ends do not lie in the same plane. (b) What is the hybridization of each of the carbon atoms in allene? (c) What orbitals overlap to form the bonds between carbon atoms in allene?arrow_forwardDescribe the bonding in the CO32 ion using the localized electron model. How would the molecular orbital model describe the bonding in this species?arrow_forward
- When two amino acids react with each other, they form a linkage called an amide group, or a peptide link. (If more linkage. are added, a protein or polypeptide is formed.) (a) What are the hybridizations of the C and N atoms in the peptide linkage? (b) Is the structure illustrated the only resonance structure possible for the peptide linkage? If another resonance structure is possible. compare it with the o ne shown. Decide which is the more important structure. (c) The computer-generated structure shown here, which contains a peptide linkage, shows that this linkage is flat. This is an important feature of proteins. Speculate on reasons that the CONH linkage is planar. What are the sites of positive and negative charge in this dipeptide?arrow_forwardDescribe the bonding in the O3 molecule and the NO2 ion, using the localized electron model. How would the molecular orbital model describe the bonding in these two species?arrow_forwardDescribe the bonding in NO+, NO, and NO, using both the localized electron and molecular orbital models. Account for any discrepancies between the two models.arrow_forward
- Identify the hybrid orbitals used by boron in BCl3 and in BCl4, the ion formed from the reaction of BCl3 and Cl. Explain your choices.arrow_forwardWhat is the OSO angle and the hybrid orbital set used by sulfur in each of the following molecules or ions? (a) SO2 (b) SO3 (c) SO32 (d) SO42 Do all have the same value for the OSO angle? Does the S atom in all these species use the same hybrid orbitals?arrow_forwardNumerous molecules are detected in deep space. Three of them are illustrated here. (a) Are these compounds isomers? (b) Indicate the hybridization of each C atom in each molecule. (c) What is the value of the HCH angle in each of the three molecules? (d) Which of these molecules is/are polar? (e) Which molecule should have the strongest carbon-carbon bond? The strongest carbon-oxygen bond?arrow_forward
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