Assuming that it has similar molecular orbital energies to those of carbon monoxide, deduce the bond order of the NO+ ion. Now compare this with the molecular orbital diagram of NO-. How did the electron configuration change from NO+ to NO-? How did this affect the molecular orbital diagram and the bond order?

Assuming that it has similar molecular orbital energies to those of carbon monoxide, deduce the bond order of the NO+ ion. Now compare this with the molecular orbital diagram of NO-. How did the electron configuration change from NO+ to NO-? How did this affect the molecular orbital diagram and the bond order?

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 10.88QE

See similar textbooks

Similar questions

In propene CH3CH=CH2, the first carbon has sp3 hybrid orbitals and the second carbon has sp2 hybrid orbitals. These orbitals interact to make a bond. Why are these hybrid orbitals not orthogonal?
Methylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) How many sigma bonds are in the molecule? (b) How many pi bonds are in the molecule? (c) What is the hybridization of the carbon atom bonded to nitrogen? (d) What is the hybridization of the carbon atom bonded to oxygen? (e) What is the hybridization of the double-bonded oxygen?
Aspirin, or acetylsalicylic acid, has the formula C9H8O4 and the skeleton structure (a) Complete the Lewis structure and give the number of bonds and bonds in aspirin. (b) What is the hybridization about the CO2H carbon atom (colored blue)? (c) What is the hybridization about the carbon atom in the benzene-like ring that is bonded to an oxygen atom (colored red)? Also, what is the hybridization of the oxygen atom bonded to this carbon atom?
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.
Strike-anywhere matches contain a layer of KClO3 and a layer of P4S3. The heat produced by the friction of striking the match causes these two compounds to react vigorously, which sets fire to the wooden stem of the match. KCIO3 contains the ClO3 ion. P4S3 is an unusual molecule with the skeletal structure. (a) Write Lewis structures for P4S3 and the ClO3 ion. (b) Describe the geometry about the P atoms, the S atom, and the Cl atom in these species. (c) Assign a hybridization to the P atoms, the S atom, and the Cl atom in these species. (d) Determine the oxidation states and formal charge of the atoms in P4S3 and the ClO3 ion.
Cinnamaldehyde ocaus naturally in cinnamon oil. (a) What is the most polar bond in the molecule? (b) How many bonds and how many bonds are there? (c) Is cis-trans isomerism possible? If so, draw the isomers of the molecule. (d) Give the hybridization of the C atoms in the molecule. (e) What are the values of the bond angles 1, 2, and 3 ?
The sulfamate ion, H2NSO3, can be thought of as having been formed from the amide ion, NH2, and sulphur trioxide, SO3. (a) What are the electron-pair and molecular geometries or the amide ion and or SO3? What are the hybridizations of the N and S atoms, respectively? (b) Sketch a structure for the sulfamate ion, and estimate the bond angles. (c) What changes in hybridization do you expect for N and S in the course of the reaction NH2 + SO3 H2NSO3? (d) Is SO3 the donor of an electron pair or the acceptor of an electron pair in the reaction with amide ion? Does the electrostatic potential map shown below confirm your prediction?
There are two compounds with the molecular formula HN3. One is called hydrogen azide; the other is cyclotriazene. (a) Write the Lewis structure for each compound. (b) Designate the hybridization of each nitrogen in hydrogen azide. (c) What is the hybridization of each nitrogen in cyclotriazene? (d) How many sigma bonds are in hydrogen azide? In cyclotriazene? (e) How many pi bonds are in hydrogen azide? In cyclotriazene? (f) Give approximate values for the N-to-N-to-N bond angles in each molecule.
Lets look more closely at the process of hybridization. (a) What is the relationship between the number of hybrid orbitals produced and the number of atomic orbitals used to create them? (b) Do hybrid atomic orbitals form between different p orbitals without involving 5 orbitals? (c) What is the relationship between the energy of hybrid atomic orbitals and the atomic orbitals from which they are formed?
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?
7.96 Consider the hydrocarbons whose structures are shown below. Which of these molecules would be planar, meaning that all of the atoms must lie in the same plane? Explain your answer in terms of orbital hybridizations.
Why is the concept of hybridization required in valence bond theory?