Exercise 2.4 Molecular Orbital Energy Level Diagrams: Homonuclear Diatomics

Similar documents
Answers to Practice Test Questions 3 Molecular Orbital Theory: Heteronuclear Diatomic Molecules

Molecular Orbitals. Based on Inorganic Chemistry, Miessler and Tarr, 4 th edition, 2011, Pearson Prentice Hall

Chapter 9. Covalent Bonding: Orbitals

Chemistry 2000 Lecture 2: LCAO-MO theory for homonuclear diatomic molecules

Practice Test Questions 4 Molecular Orbital Theory: Polyatomic Molecules

Chapter 9. Covalent Bonding: Orbitals

Chapter 10. VSEPR Model: Geometries

Ch. 9 Practice Questions

Chapter 9. Molecular Geometries and Bonding Theories. Lecture Presentation. John D. Bookstaver St. Charles Community College Cottleville, MO

Chemistry: The Central Science. Chapter 9: Molecular Geometry and Bonding Theory

Chapter 9. Covalent Bonding: Orbitals. Copyright 2017 Cengage Learning. All Rights Reserved.

Chapter 9 Molecular Geometry and Bonding Theories

Chapter 10. VSEPR Model: Geometries

Chapter 4. Molecular Structure and Orbitals

11/29/2014. Problems with Valence Bond Theory. VB theory predicts many properties better than Lewis Theory

Chem Spring, 2017 Assignment 5 - Solutions

Chapter 14: Phenomena

Chapter 10: Chemical Bonding II. Bonding Theories

ANNOUNCEMENTS. If you have questions about your exam 2 grade, write to me or Chapter 8 homework due April. 13 th.

Activity Molecular Orbital Theory

CHEM J-5 June 2014

Chapter 9. Molecular Geometry and Bonding Theories

Chapter 8. Molecular Shapes. Valence Shell Electron Pair Repulsion Theory (VSEPR) What Determines the Shape of a Molecule?

Chapter 9. Molecular Geometry and Bonding Theories

Atomic combinations: Covalent bonding and Lewis notation *

Shapes of Molecules. Lewis structures are useful but don t allow prediction of the shape of a molecule.

Chapter 9. Molecular Geometries and Bonding Theories. Lecture Presentation. John D. Bookstaver St. Charles Community College Cottleville, MO

Be H. Delocalized Bonding. Localized Bonding. σ 2. σ 1. Two (sp-1s) Be-H σ bonds. The two σ bonding MO s in BeH 2. MO diagram for BeH 2

Chapter 9. Molecular Geometry and Bonding Theories

COVALENT BONDING: ORBITALS

ANNOUNCEMENTS. If you have questions about your exam 2 grade, write to me or Chapter 7 homework due Nov, 9 th.

Chapter 9: Molecular Geometry and Bonding Theories

Molecular-Orbital Theory

Chapter 9. Chemical Bonding II: Molecular Geometry and Bonding Theories

Can atomic orbitals explain these shapes or angles? What s in Chapter 9: Shapes of molecules affect: reactivity physical properties

SHAPES OF MOLECULES (VSEPR MODEL)

Activity Molecular Orbital Theory

Name Honors Chemistry / /

Molecular Geometry and Bonding Theories. Chapter 9

Inorganic Chemistry with Doc M. Day 18. Transition Metals Complexes IV: Ligand Field Theory continued

Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals

Valence Bond Theory. Localized Electron Model. Hybridize the Orbitals! Overlap and Bonding. Atomic Orbitals are. mmmkay. Overlap and Bonding

Chapter 10 Chemical Bonding II

Be H. Delocalized Bonding. Localized Bonding. σ 2. σ 1. Two (sp-1s) Be-H σ bonds. The two σ bonding MO s in BeH 2. MO diagram for BeH 2

Name. CHM 115 EXAM #2 Practice KEY. a. N Cl b. N F c. F F d. I I e. N Br. a. K b. Be c. O d. Al e. S

CHEMISTRY. Chapter 8 ADVANCED THEORIES OF COVALENT BONDING Kevin Kolack, Ph.D. The Cooper Union HW problems: 6, 7, 12, 21, 27, 29, 41, 47, 49

Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals

CHAPTER 5: Bonding Theories - Explaining Molecular Geometry. Chapter Outline

Chapter 9 Molecular Geometry and Bonding Theories

5.111 Principles of Chemical Science

Chapter 9. and Bonding Theories

A DOT STRUCTURE FOR A LARGER MOLECULE ETHANOL! Count valence electrons

Chapter 9: Molecular Geometries and Bonding Theories Learning Outcomes: Predict the three-dimensional shapes of molecules using the VSEPR model.

Covalent Bonding 10/29/2013

Molecular Bond Theory

Molecular Shapes and VSEPR (Valence Shell Electron Pair Repulsion Theory)

Chapter 9. and Bonding Theories. Molecular Shapes. What Determines the Shape of a Molecule? 3/8/2013

In this lecture we will understand how the molecular orbitals are formed from the interaction of atomic orbitals.

Chapter 10: Chemical Bonding II: Molecular Shapes; VSEPR, Valence Bond and Molecular Orbital Theories

CHAPTER TEN MOLECULAR GEOMETRY MOLECULAR GEOMETRY V S E P R CHEMICAL BONDING II: MOLECULAR GEOMETRY AND HYBRIDIZATION OF ATOMIC ORBITALS

Topic 2. Structure and Bonding Models of Covalent Compounds of p-block Elements

Section 8.1 The Covalent Bond

CHEMISTRY & YOU What is the difference between the oxygen you breathe and the oxygen in ozone in the atmosphere?

Chapter 10 Chemical Bonding II: Molecular Shapes, Valence Bond Theory, and Molecular Orbital Theory

Molecular Orbital Theory This means that the coefficients in the MO will not be the same!

Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals Chapter 10

Learning Guide 2C Small Molecules Chem What are the two most common types of physical changes that we encounter in chemistry?

Lecture 14 Chemistry 362 M. Darensbourg 2017 Spring term. Molecular orbitals for diatomics

Section 8.13 Molecular Hybridization Structure: The VSEPR Model

5.111 Lecture Summary #13 Monday, October 6, 2014

Chemical Bonding. Lewis Theory-VSEPR Valence Bond Theory Molecular Orbital Theory

Valence bond theory accounts, at least qualitatively, for the stability of the covalent bond in terms of overlapping atomic orbitals.

Organic Chemistry. Review Information for Unit 1. VSEPR Hybrid Orbitals Polar Molecules

Chapter 9. Covalent Bonding: Orbitals

Bonding and Physical Properties The Molecular Orbital Theory

Homework #7. Chapter 14. Covalent Bonding Orbitals

Valence Bond Model and Hybridization

End of chapter exercises

Molecular Orbitals. Chapter 9. Sigma bonding orbitals. Sigma bonding orbitals. Pi bonding orbitals. Sigma and pi bonds

Molecular Orbitals in Chemical Bonding

A Rigorous Introduction to Molecular Orbital Theory and its Applications in Chemistry. Zachary Chin, Alex Li, Alex Liu

5 Polyatomic molecules

Theoretical Chemistry - Level II - Practical Class Molecular Orbitals in Diatomics

Instant download Test bank for Chemistry The Central Science 10th Edition by Brown, LeMay, Bursten CLICK HERE

17/11/2010. Lewis structures

TYPES OF SYMMETRIES OF MO s s-s combinations of orbitals: , if they are antibonding. s-p combinatinos of orbitals: CHEMICAL BONDING.

Lecture Notes D: Molecular Orbital Theory

Chapter 9 - Covalent Bonding: Orbitals

Chapter 10. Geometry

Ch. 9- Molecular Geometry and Bonding Theories

What Do Molecules Look Like?

MOLECULAR ORBITAL THEORY Chapter 10.8, Morrison and Boyd

Molecular Geometry. Dr. Williamson s Molecular Geometry Notes. VSEPR: Definition of Terms. Dr. V.M. Williamson Texas A & M University Student Version

Molecular Geometry. Dr. Williamson s Molecular Geometry Notes. VSEPR: Definition of Terms. VSEPR: Electronic Geometries VSEPR

Coordinate Covalent Bond

Molecular Structure and Orbitals

Chapter 9 Molecular Geometry Valence Bond and Molecular Orbital Theory

Chapter 10 Theories of Covalent Bonding

CHAPTER 9 COVALENT BONDING: ORBITALS. Questions

Covalent Bonding and Molecular Structures

Transcription:

Exercise 2.4 Molecular rbital Energy Level Diagrams: Homonuclear Diatomics This exercise assumes that you are familiar with the count and sort algorithm described in Exercise 2.3. The table of atomic orbital energies is repeated below for easy reference. Table of Atomic rbital Energies. All Energies are in Ry. 1s H -1.00 He -1.81 Li -4.77-0.40 Be -8.9-0.69 B -14.5-1.03-0.42 C -21.6-1.43-0.79-30.0-1.88-0.95-39.9-2.38-1.17 F -51.2-2.95-1.37 e -64.0-3.56-1.59 All energies are from J.C. Slater Physical Review (1955) 98, 1039-1045. Molecular rbital Energy Level Diagrams for 22, FF 22, and 22 In oxygen, fluorine and neon atoms, the difference between the energies of the s and p orbitals is greater than 1 Ry. As such, we can assume that there is no significant interaction between the s and p orbitals. Thus, when we group the atomic orbitals (As) by symmetry and energy, there are four distinct groups: two pi-symmetric p yy orbitals, one from each atom, two sigma-symmetric s orbitals, one from each atom, and two sigma-symmetric p zz orbitals, one from each atom. Each group makes two molecular orbitals (Ms) of the appropriate symmetry. Molecular rbital Energy Level Diagrams for BB 22, CC 22, and 22 In boron, carbon and nitrogen atoms, the difference between the energies of the s and p orbitals is less than 1 Ry. As such, there is significant interaction between the s and p orbitals. Thus, when we group the As by symmetry and energy, there are only three groups: two pi-symmetric p yy orbitals, one from each atom, and four sigma-symmetric orbitals, both s and p zz from each atom. All four sigma-symmetric As (s and p zz on both atoms) combine to make a set of four sigmasymmetric Ms. This lowers the energy of the 2σσ orbital and raises the energy of the 3σσ orbital (relative to where they would have been if the s and p zz orbitals did not interact). The most notable consequence of this interaction is that the energy of the 3σσ orbital is raised enough that it becomes higher in energy than the 1ππ orbitals.

Molecular rbital Energy Level Diagram for 22 First, the electron configuration for each oxygen atom is written: 1ss 2 s 2 p 4 This tells us that the valence shell for each oxygen atom is nn = 2, and that the valence As are the s and p orbitals. It also tells us that 2 has twelve valence electrons. A Lewis diagram for 2 is shown below and, since there are only two atoms, it must be linear. Grouping the As by symmetry and energy gives: two pi-symmetric p yy orbitals, one from each atom, two sigma-symmetric s orbitals, one from each atom, and two sigma-symmetric p zz orbitals, one from each atom. Each group makes two Ms, one bonding and one antibonding. The bonding M is lower in energy than the As from which it was made, and the antibonding M is higher in energy than the As from which it was made. The Ms made from p orbitals are higher in energy than the Ms made from s orbitals. Because the electron density in 3σσ is concentrated along the line between the nuclei, 3σσ is lower in energy than the 1ππ Ms. For similar reasons, 4σσ is higher in energy than 2ππ. Following the remaining steps of the algorithm gives this M energy level diagram: 4 σ 2 π E 1 π 3 σ 2 σ 1 σ Bond order for 2 can be calculated: 8 4 = 4 = 2 and is consistent with the double bond observed 2 2 on the Lewis diagram. Where this diagram differs from the Lewis diagram is that it shows that 2 has two unpaired electrons. This explains why 2 behaves as a paramagnetic substance. All reactions of 2 are expected to involve the 2ππ Ms; they contain the highest energy electrons *and* the lowest unoccupied spaces for new electrons to be added. So, 2ππ is functioning as both HM and LUM. Alternatively, it can be labeled SM (Singly ccupied Molecular rbital). 2

Molecular rbital Energy Level Diagram for 22 First, the electron configuration for each nitrogen atom is written: 1ss 2 s 2 p 3 This tells us that the valence shell for each oxygen atom is nn = 2, and that the valence As are the s and p orbitals. It also tells us that 2 has ten valence electrons. A Lewis diagram for 2 is shown below and, since there are only two atoms, it must be linear. Grouping the As by symmetry and energy gives: two pi-symmetric p yy orbitals, one from each atom, and four sigma-symmetric orbitals, both s and p zz from each atom. This first two groups each make two Ms, one bonding and one antibonding. There is no energy difference between the ππ xx and ππ yy orbitals. The last group makes four Ms, two bonding and two antibonding. The lowest energy M is lower in energy than all four As. The highest energy M is higher in energy than all four As. As noted on the first page of this exercise, the 3σσ orbital is higher in energy than the 1ππ orbitals. Following the remaining steps of the algorithm gives this molecular orbital energy level diagram: 4 σ 2 π E 3 σ 1 π 2 σ 1 σ 2 As you can see, the diagram is starting to look cluttered due to the large number of tie lines. As molecules get larger, this problem gets worse, so they re typically only used for small molecules. Bond order for 2 can be calculated: 8 2 = 6 = 3 and is consistent with the triple bond observed 2 2 on the Lewis diagram. The HM is 3σσ, so those are the electrons donated in reactions where 2 is an electron donor. The LUM is 2ππ, so that is where electrons will be added in reactions where 2 is an electron acceptor. Since electrons would either be donated from a bonding orbital or added to an antibonding orbital, any reaction of 2 will reduce the - bond order.

1. Add pictures of the atomic orbitals and molecular orbitals to the molecular orbital energy level diagrams of 2 and 2 provided in the preceding text. 2. Write valence orbital occupancies for 2 and 2 based on the molecular orbital energy level diagrams provided in the preceding text. (a) 2 (b) 2 3. (a) Construct a molecular orbital energy level diagram for FF 2. (b) How does the diagram change if two electrons are added? What does this tell you about what happens when two electrons are added to FF 2?

4. (a) Construct a molecular orbital energy level diagram for CC 2. (b) How does the diagram change if two electrons are added? What does this tell you about what happens when two electrons are added to CC 2?

5. In CCCC 2, there is not enough interaction between the 3ss and 3pp orbitals to raise the energy of the 3σσ M higher than that of the 1ππ Ms. Knowing this, construct a molecular orbital energy level diagram for CCCC 2. Draw pictures of each molecular orbital on or next to your diagram. It must be clear which picture corresponds to each labeled energy level. How does this diagram compare to the diagram you drew for FF 2 in question 2?