Using the molecular orbital energy ordering for second-row ho-monuclear diatomic molecules in which the 2, orbitals lie athigher energy than the a, draw MO energy diagrams and pre-dict the bond order in a molecule or ion with each number oftotal valence electrons. Will the molecule or ion be diamagneticor paramagnetic?a. 10b. 12с. 13d. 14

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Chemistry: Principles and Practice

3rd Edition

ISBN:9780534420123

Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Publisher:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Chapter10: Molecular Structure And Bonding Theories

Section: Chapter Questions

Problem 10.97QE

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The diatomic molecule OH exists in the gas phase. The bond length and bond energy have been measured to be 97.06 pm and 424.7 kJ/mol, respectively. Assume that the OH molecule is analogous to the HF molecule discussed in the chapter and that molecular orbitals result from the overlap of a lowerenergy pz, orbital from oxygen with the higher-energy ls orbital of hydrogen (the OH bond lies along the z-axis). a. Which of the two molecular orbitals will have the greater hydrogen 1s character? b. Can the 2px orbital of oxygen form molecular orbitals with the 1s orbital of hydrogen? Explain. c. Knowing that only the 2p orbitals of oxygen will interact significantly with the 1s orbital of hydrogen, complete the molecular orbital energy-level diagram for OH. Place the correct number of electrons in the energy levels. d. Estimate the bond order for OH. e. Predict whether the bond order of OH+ will be greater than, less than, or the same as that of OH. Explain.
Write the molecular orbital configuration of the diatomic molecule BN. What is the bond order of BN? Is the substance diamagnetic or paramagnetic? Use the order of energies that was given for homonuelcar diatomic molecules.
Why is the concept of hybridization required in valence bond theory?
Compare and contrast the molecular orbital and ionic bonding descriptions of LiF.
Identify the hybrid orbitals used by antimony in SbCl5 and in SbCl6, the ion formed from the reaction of SbCl5 and Cl. Explain your choices.
Do lone pairs about a central atom affect the hybridization of the central atom? If so, how?
Predict 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+
What hybrid orbitals would be expected for the central atom in each of the following molecules or ions?
The molecular orbital diagram of NO shown in Figure 10.47 also applies to the following species. Write the molecular orbital electron configuration of each, indicating the bond order and the number of unpaired electrons. (a) CN (b) CO (c) BeB (d) BC+ Figure 10.47 Molecular orbital diagram for nitric oxide (NO). The molecular orbital diagram for NO predicts a bond order of 2.5 and predicts that the molecule is paramagnetic with one unpaired electron. These predictions are verified by experimental measurements.
Solid sulfur normally consists of crystals of S8 molecules, but when heated strongly, the solid vaporizes to give S2 molecules (among other molecular species). Describe the bonding in S2 in molecular orbital terms, assuming the orbitals are analogous to those of the preceding period. What would you expect to happen to the sulfur sulfur bond length if two electrons were added to give the S22 ion? What would you expect to happen to the bond length if, instead, two electrons were taken away to give S22+?
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.
The structure of amphetamine, a stimulant, is shown below. (Replacing one H atom on the NH2, or amino, group with CH3 gives methamphetamine a particularly dangerous drug commonly known as speed.) (a) What are the hybrid orbitals used by the C atoms of the C6 ring. by the C atoms of the side chain, and by the N atom? (b) Give approximate values for the bond angles A, B, and C. (c) How many bonds and bonds are in the molerule? (d) Is the molecule polar or nonpolar? (e) Amphetamine reacts readily with a proton (H+) in aqueous solution. Where does this proton attach to the molecule? Explain how the electrostatic potential map predicts this site of protonation.

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