(a)
Interpretation:
The MO diagram, the number of unpaired electrons, the number bonds in
Concept Introduction:
Molecular orbital theory:
The atomic orbitals of the atoms constituted in a molecule are combined to produce new orbitals are called Molecular Orbitals.
Like atomic orbitals, a molecular orbital can accommodate maximum two electrons and the two electrons must have opposite spins (Pauli Exclusion Principle).
The numbers of MO’s are equals to the number of atomic orbitals are combined in such a way that the linear combination of similar atomic orbitals to form one bonding and one anti-bonding MO’s.
The bonding MO’s are lower in energy than the anti-bonding MO’s.
HOMO is the highest energized occupied orbital in the MO’s.
Relative energy levels of molecules are according to the energy levels of atomic orbitals.
LUMO is the lowest energized orbital in the MO’s.
Bond order can be calculated using below formula
(a)

Explanation of Solution
The total number of valence electrons present in
The molecular orbital diagrams of the
The bond order can be calculated using bonding and anti-bonding orbitals, the bond order is
Therefore, the
(b)
Interpretation:
The MO diagram, the number of unpaired electrons, the number bonds in
Concept Introduction:
Refer part (a).
(b)

Explanation of Solution
The total number of valence electrons present in
The molecular orbital diagrams of the
The bond order can be calculated using bonding and anti-bonding orbitals, the bond order is
Therefore, the
(c)
Interpretation:
The MO diagram, the number of unpaired electrons, the number bonds in
Concept Introduction:
Refer part (a).
(c)

Explanation of Solution
The total number of valence electrons present in
The molecular orbital diagrams of the
The bond order can be calculated using bonding and anti-bonding orbitals, the bond order is
Therefore, the
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Chapter 6 Solutions
OWLV2 FOR MOORE/STANITSKI'S CHEMISTRY:
- Interpreting NMR spectra is a skill that often requires some amount of practice, which, in turn, necessitates access to a collection of NMR spectra. Beyond Labz Organic Synthesis and Organic Qualitative Analysis have spectral libraries containing over 700 1H NMR spectra. In this assignment, you will take advantage of this by first predicting the NMR spectra for two closely related compounds and then checking your predictions by looking up the actual spectra in the spectra library. After completing this assignment, you may wish to select other compounds for additional practice. 1. Write the IUPAC names for the following two structures: Question 2 Question 3 2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled**arrow_forward11:14 ... worksheets.beyondlabz.com 3. To check your predictions, click this link for Interpreting NMR Spectra 1. You will see a list of all the - compounds in the spectra library in alphabetical order by IUPAC name. Hovering over a name in the list will show the structure on the chalkboard. The four buttons on the top of the Spectra tab in the tray are used to select the different spectroscopic techniques for the selected compound. Make sure the NMR button has been selected. 4. Scroll through the list of names to find the names for the two compounds you have been given and click on the name to display the NMR spectrum for each. In the NMR tables below, list the chemical shift, the splitting, and the number of hydrogens associated with each peak for each compound. Compare your answers to your predictions. **Not all slots must be filled** Peak Chemical Shift (d) Multiplicity 1 2 3 4 5arrow_forwardО δα HO- H -Br δα HO-- + + -Br [B] 8+ HO- -Br δα नarrow_forward
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