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Why does the molecular orbital model do a better job in explaining the bonding in NO-and NO then the hybrid orbital model?

Short Answer

Expert verified

The molecular orbital model does a better job in explaining the bonding in NO-and NO because it can predict the accurate bond order and bonding pattern of the molecule whereas the hybridization model fails to do so.

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01

Determine the electronic configuration

Electronic configuration N atom: 1s22s22p3

Electronic configuration O atom:1s22s22p4

Molecular orbital configuration of NO is

σ1s2σ1s*2σ2s2σ2s*2π2px2π2py2σ2px2π2px*1

Molecular orbital configuration of NO-

σ1s2σ1s*2σ2s2σ2s*2π2px2π2py2σ2px2π2px*2

02

Determine the bond order 

Bond order of NO-:122a10-6=2

Bond order of NO:12210-5=25

03

Explanation

Electrons are present in antibonding π orbitals which helps to predict the bonding pattern whereas the hybrid model fails to do so.

The molecular orbital model does a better job in explaining the bonding in and NO because it can predict the accurate bond order and bonding pattern of the molecule whereas the hybridization model fails to do so.

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Most popular questions from this chapter

Which of the following would you expect to be more favorable energetically? Explain.

a. An H2 molecule in which enough energy is added to excite one electron from a bonding to an antibonding MO

b. Two separate H atoms

The diatomic molecule OH exist in the gas phase. OH plays an important role in combustion reaction and is a reactive oxidizing agent in polluted air. 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 the MOs result from the overlap of pz orbital from oxygen and 1s orbital of hydrogen. (The O-H bond lies along the z-axis)

a. Draw a picture of the sigma bonding and antibonding molecular orbitals in OH.

b. Which of the two MOs has the greater hydrogen 1s character?

c. Can the 2px orbital of oxygen form MOs with 1s orbital of hydrogen? Explain.

d. Knowing that only the 2p orbitals of oxygen interact significantly with the 1s orbital of hydrogen, complete the MO diagram for OH. Place the correct number of electrons in the energy level.

e. Estimate the bond order for OH

f. Predict whether the bond order of OH+ is greater than, lesser than, or the same as that of OH+. Explain.

For each of the following chemical formulas, an NMR spectrum is described, including relative overall areas (intensities) for the various signals given in parentheses. Draw the structure of a compound having the specific formula that would give the described NMR spectrum. Hint: All of these formulas represent organic compounds. Lewis structures for organic compounds typically have all atoms in the compound with a formal charge of zero. This is the case in this problem.)

a.C2H3Cl3;NMRhas one singlet signal.

b.C3H6Cl2;NMRhas a triplet (4) and a quintet (2) signal.

c.C3H6O2; NMR has a singlet (1), a quartet (2), and a triplet (3)signal.

d.C5H10O; NMR has a heptet (1), a singlet (3), and a doublet (6) signal.

e.C3H6O;NMRhas a triplet (3), a quintet (2), and a triplet (1) signal.

In exercise 71 in chapter 13 the lewis structure for benzene was drawn. Using one of the lewis structures estimate Hffor C6H6(g). Using bond energies and given standard enthalpies of formation of C(g) is 717kJ/mol. The experimental Hffor C6H6is 83 kJ/mol. Explain the discrepancy between the experimental value and the calculated Hfvalue of C6H6(g).

Describe the bonding in the first excited state of N2 (the one closest in energy to the ground state) using the MO model. What differences do you expect in the properties of the molecule in the ground state and in the first excited state? (An excited state of a molecule corresponds to an electron arrangement other than that giving the lowest possible energy.)

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