
PHYSICAL CHEMISTRY-STUDENT SOLN.MAN.
2nd Edition
ISBN: 9781285074788
Author: Ball
Publisher: CENGAGE L
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Chapter 10, Problem 10.80E
Interpretation Introduction
Interpretation:
The Hamiltonian operator, acceptable wavefunctions, and the quantized energies of a particle in a two-dimensional box are to be stated.
Concept introduction:
The Schrödinger equation is used to find the allowed energy levels for electronic transitions in the
Where,
•
•
•
The energy obtained after applying the operator on wavefunction is known as the eigen value for the wavefunction.
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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 10 Solutions
PHYSICAL CHEMISTRY-STUDENT SOLN.MAN.
Ch. 10 - State the postulates of quantum mechanics...Ch. 10 - Prob. 10.2ECh. 10 - State whether the following functions are...Ch. 10 - State whether the following functions are...Ch. 10 - Prob. 10.5ECh. 10 - Prob. 10.6ECh. 10 - Evaluate the operations in parts a, b, and f in...Ch. 10 - The following operators and functions are defined:...Ch. 10 - Prob. 10.9ECh. 10 - Indicate which of these expressions yield...
Ch. 10 - Indicate which of these expressions yield an...Ch. 10 - Why is multiplying a function by a constant...Ch. 10 - Prob. 10.13ECh. 10 - Using the original definition of the momentum...Ch. 10 - Under what conditions would the operator described...Ch. 10 - A particle on a ring has a wavefunction =12eim...Ch. 10 - Calculate the uncertainty in position, x, of a...Ch. 10 - For an atom of mercury, an electron in the 1s...Ch. 10 - Classically, a hydrogen atom behaves as if it were...Ch. 10 - The largest known atom, francium, has an atomic...Ch. 10 - How is the Bohr theory of the hydrogen atom...Ch. 10 - Though not strictly equivalent, there is a similar...Ch. 10 - The uncertainty principle is related to the order...Ch. 10 - Prob. 10.24ECh. 10 - Prob. 10.25ECh. 10 - For a particle in a state having the wavefunction...Ch. 10 - Prob. 10.27ECh. 10 - A particle on a ring has a wavefunction =eim,...Ch. 10 - Prob. 10.29ECh. 10 - Prob. 10.30ECh. 10 - Prob. 10.31ECh. 10 - Normalize the following wavefunctions over the...Ch. 10 - Prob. 10.33ECh. 10 - Prob. 10.34ECh. 10 - For an unbound or free particle having mass m in...Ch. 10 - Prob. 10.36ECh. 10 - Prob. 10.37ECh. 10 - Prob. 10.38ECh. 10 - Evaluate the expression for the total energies for...Ch. 10 - Prob. 10.40ECh. 10 - Verify that the following wavefunctions are indeed...Ch. 10 - In exercise 10.41a, the wavefunction is not...Ch. 10 - Prob. 10.43ECh. 10 - Prob. 10.44ECh. 10 - Explain why n=0 is not allowed for a...Ch. 10 - Prob. 10.46ECh. 10 - Prob. 10.47ECh. 10 - Prob. 10.48ECh. 10 - Carotenes are molecules with alternating CC and...Ch. 10 - The electronic spectrum of the molecule butadiene,...Ch. 10 - Prob. 10.51ECh. 10 - Prob. 10.52ECh. 10 - Show that the normalization constants for the...Ch. 10 - Prob. 10.54ECh. 10 - Prob. 10.55ECh. 10 - An official baseball has a mass of 145g. a...Ch. 10 - Is the uncertainty principle consistent with our...Ch. 10 - Prob. 10.58ECh. 10 - Prob. 10.59ECh. 10 - Instead of x=0 to a, assume that the limits on the...Ch. 10 - In a plot of ||2, the maximum maxima in the plot...Ch. 10 - Prob. 10.62ECh. 10 - Prob. 10.63ECh. 10 - The average value of radius in a circular system,...Ch. 10 - Prob. 10.65ECh. 10 - Prob. 10.66ECh. 10 - Prob. 10.67ECh. 10 - Prob. 10.68ECh. 10 - Prob. 10.69ECh. 10 - Assume that for a particle on a ring the operator...Ch. 10 - Mathematically, the uncertainty A in some...Ch. 10 - Prob. 10.72ECh. 10 - Prob. 10.73ECh. 10 - Verify that the wavefunctions in equation 10.20...Ch. 10 - An electron is confined to a box of dimensions...Ch. 10 - a What is the ratio of energy levels having the...Ch. 10 - Consider a one-dimensional particle-in-a-box and a...Ch. 10 - Prob. 10.78ECh. 10 - Prob. 10.79ECh. 10 - Prob. 10.80ECh. 10 - Prob. 10.81ECh. 10 - What are x,y, and z for 111 of a 3-D...Ch. 10 - Prob. 10.83ECh. 10 - Prob. 10.84ECh. 10 - Prob. 10.85ECh. 10 - Prob. 10.86ECh. 10 - Prob. 10.87ECh. 10 - Prob. 10.88ECh. 10 - Substitute (x,t)=eiEt/(x) into the time-dependent...Ch. 10 - Write (x,t)=eiEt/(x) in terms of sine and cosine,...Ch. 10 - Prob. 10.91ECh. 10 - Prob. 10.92ECh. 10 - Prob. 10.93ECh. 10 - Prob. 10.95E
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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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