Mastering Chemistry with Pearson eText -- Standalone Access Card -- for Chemistry: Structure and Properties (2nd Edition)
2nd Edition
ISBN: 9780134566290
Author: Nivaldo J. Tro
Publisher: PEARSON
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Chapter 6, Problem 17E
Interpretation Introduction
Interpretation:
“The relation between the number of molecular orbitals formed by the linear combination of atomic orbitals and the number of atomic orbitals used in the approximation” should be explained.
Concept introduction:
► Atomic orbital is a mathematical function which depicts the location of electron in an atom whereas Molecular orbital is mathematical function which describes the possible location of an electron in a molecule as whole.
► Molecular orbitals can be of three types: Bonding, non-bonding and anti-bonding.
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5 (a). Using the peak information you listed in the tables for
both structures, assign each peak to that portion of the
structure that produces the peak in the NMR spectrum. Draw
this diagram on your own sheet of paper and attach the sketch
of your drawing to this question.
Question 6
5 (b). Using the peak information you listed in the tables for
both structures, assign each peak to that portion of the
structure that produces the peak in the NMR spectrum. Draw
this diagram on your own sheet of paper and attach the sketch
of your drawing to this question.
Question 7
6. Are there any differences between the spectra you obtained
in Beyond Labz and the predicted spectra? If so, what were
the differences?
<
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**
Peak
Chemical Shift (d)
5.7
1
Multiplicity
multiplate
..........
5.04
double of doublet
2
4.98
double of doublet
3
4.05
doublet of quartet
4
5
LO
3.80
quartet
1.3
doublet
6
Peak
Chemical Shift (d)
Multiplicity
Chapter 6 Solutions
Mastering Chemistry with Pearson eText -- Standalone Access Card -- for Chemistry: Structure and Properties (2nd Edition)
Ch. 6 - Prob. 1ECh. 6 - What is a chemical bond according to valence bond...Ch. 6 - In valence bond theory, what determines the...Ch. 6 - In valence bond theory, the interaction energy...Ch. 6 - What is hybridization? Why is hybridization...Ch. 6 - How does hybridization of the atomic orbitals in...Ch. 6 - How is the number of hybrid orbitals related to...Ch. 6 - Sketch each hybrid orbital sp sp2 sp3 sp3d sp3d2Ch. 6 - Prob. 9ECh. 6 - Name the hybridization scheme that corresponds to...
Ch. 6 - What is a chemical bond according to molecular...Ch. 6 - Explain the difference between hybrid atomic...Ch. 6 - What is a bonding molecular orbital?Ch. 6 - Prob. 14ECh. 6 - What is the role of wave interference in...Ch. 6 - Prob. 16ECh. 6 - Prob. 17ECh. 6 - Prob. 18ECh. 6 - Prob. 19ECh. 6 - Prob. 20ECh. 6 - Prob. 21ECh. 6 - When applying molecular orbital theory to...Ch. 6 - In molecular orbital theory, what is a nonbonding...Ch. 6 - Write a short paragraph describing chemical...Ch. 6 - The valence electron configurations of several...Ch. 6 - The valence electron configurations of several...Ch. 6 - Draw orbital diagrams (boxes with arrows in them)...Ch. 6 - Draw orbital diagrams (boxes with arrows in them)...Ch. 6 - Prob. 29ECh. 6 - Draw orbital diagrams (boxes with arrows in them)...Ch. 6 - Which hybridization scheme allows the formation of...Ch. 6 - Which hybridization scheme allows the central atom...Ch. 6 - Write a hybridization and bonding scheme for each...Ch. 6 - Write a hybridization and bonding scheme for each...Ch. 6 - Write a hybridization and bonding scheme for each...Ch. 6 - Write a hybridization and bonding scheme for each...Ch. 6 - Write a hybridization and bonding scheme for each...Ch. 6 - Write a hybridization and bonding scheme for each...Ch. 6 - Consider the structure of the amino acid alanine...Ch. 6 - Consider the structure of the amino acid aspartic...Ch. 6 - Sketch the bonding molecular orbital that results...Ch. 6 - Sketch the antibonding molecular orbital that...Ch. 6 - Draw an MO energy diagram and predict the bond...Ch. 6 - Draw an MO energy diagram and predict the bond...Ch. 6 - Sketch the bonding and antibonding molecular...Ch. 6 - Sketch the bonding and antibonding molecular...Ch. 6 - Using the molecular orbital energy ordenng for...Ch. 6 - Using the molecular orbital energy ordering for...Ch. 6 - Apply molecular orbital theory to predict if each...Ch. 6 - Apply molecular orbital theory to predict if each...Ch. 6 - According to MO theory, which molecule or ion has...Ch. 6 - According to MO theory, which molecule or ion has...Ch. 6 - Draw an MO energy diagram for CO. (Use the energy...Ch. 6 - Draw an MO energy diagram for HCI. Predict the...Ch. 6 - For each compound, draw the Lewis structure,...Ch. 6 - For each compound, draw the Lewis structure,...Ch. 6 - Amino acids are biological compounds that link...Ch. 6 - The genetic code is based on four different bases...Ch. 6 - The structure of caffeine, present in coffee and...Ch. 6 - The structure of acetylsalicylic acid (aspirin) is...Ch. 6 - Draw a molecular orbital energy diagram for CIF....Ch. 6 - Draw Lewis structures and MO diagrams for CN+, CN,...Ch. 6 - Bromine can form compounds or ions with any number...Ch. 6 - The compound C3H4 has two double bonds. Describe...Ch. 6 - How many hybrid orbitals do we use to describe...Ch. 6 - Prob. 66ECh. 6 - In VSEPR theory, which uses the Lewis model to...Ch. 6 - The resuts of a molecular orbital calculation for...Ch. 6 - Prob. 69ECh. 6 - cis-2-Butene isomerizes (changes its structure) to...Ch. 6 - The ion CH5 + can form under very special...Ch. 6 - Neither the VSEPR model nor the hybridization...Ch. 6 - Prob. 73ECh. 6 - The most stable forms of the nonmetals in groups...Ch. 6 - Consider the bond energies of three iodine...Ch. 6 - How many atomic orbitals form a set of sp3hybrid...Ch. 6 - Have each group member pick one of these...Ch. 6 - Divide your group into two subgroups. Have one...Ch. 6 - A molecular orbital calculation for Hi results in...Ch. 6 - Determine the hybridization about 0 in CH3OH.Ch. 6 - Determine the hybridization about C in H2CO.Ch. 6 - According to the valance bond theory, which kind...Ch. 6 - Use molecular orbital theory to determine the bond...Ch. 6 - Use molecular orbital theory to predict which...Ch. 6 - Use molecular orbital theory to determine which...Ch. 6 - Which hybridization scheme occurs about nitrogen...Ch. 6 - Prob. 8SAQCh. 6 - Prob. 9SAQCh. 6 - Prob. 10SAQCh. 6 - Which type of orbitals overlap to form the sigma...
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- 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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