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OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
5th Edition
ISBN: 9781285460420
Author: John W. Moore; Conrad L. Stanitski
Publisher: Cengage Learning US
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Chapter 2.11, Problem 2.20CE
Interpretation Introduction
Interpretation:
The given statement “Two different compounds have the same formula. Therefore,
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⚫ worksheets.beyondlabz.com
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 2 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
Ch. 2.1 - When you comb your hair on a dry day, your hair...Ch. 2.2 - Prob. 2.1PSPCh. 2.2 - Prob. 2.2PSPCh. 2.2 - Prob. 2.2CECh. 2.2 - Prob. 2.3PSPCh. 2.3 - Prob. 2.4PSPCh. 2.3 - A student in your chemistry class tells you that...Ch. 2.3 - Prob. 2.5PSPCh. 2.3 - Prob. 2.4CECh. 2.3 - Prob. 2.5CE
Ch. 2.4 - Prob. 2.6PSPCh. 2.4 - Prob. 2.6CECh. 2.4 - Prob. 2.7PSPCh. 2.4 - Prob. 2.8PSPCh. 2.5 - Prob. 2.9PSPCh. 2.5 - Prob. 2.10PSPCh. 2.6 - Prob. 2.7CECh. 2.7 - Prob. 2.8CECh. 2.7 - Prob. 2.11PSPCh. 2.7 - Prob. 2.9ECh. 2.8 - Prob. 2.12PSPCh. 2.8 - Prob. 2.10ECh. 2.9 - Prob. 2.11ECh. 2.9 - Prob. 2.12ECh. 2.9 - Prob. 2.13CECh. 2.9 - According to Table 2.10, five constitutional...Ch. 2.11 - Calculate (a) the amount of Ti atoms in 4.00 g...Ch. 2.11 - Prob. 2.15CECh. 2.11 - Prob. 2.16ECh. 2.11 - Prob. 2.17CECh. 2.11 - Prob. 2.18ECh. 2.11 - Prob. 2.19ECh. 2.11 - Prob. 2.14PSPCh. 2.11 - Prob. 2.15PSPCh. 2.11 - Prob. 2.16PSPCh. 2.11 - Prob. 2.20CECh. 2.12 - Prob. 2.17PSPCh. 2.12 - Prob. 2.18PSPCh. 2.12 - Prob. 2.21ECh. 2.12 - Hydrazine is composed of 87.42% nitrogen and...Ch. 2.12 - Prob. 2.20PSPCh. 2.12 - Prob. 2.22ECh. 2 - An isotope of an element contains 63 protons and...Ch. 2 - Prob. IISPCh. 2 - Prob. IIISPCh. 2 - Dioxathion, a pesticide, contains carbon,...Ch. 2 - Prob. 1QRTCh. 2 - Prob. 2QRTCh. 2 - Prob. 3QRTCh. 2 - Prob. 4QRTCh. 2 - Prob. 5QRTCh. 2 - Prob. 6QRTCh. 2 - Prob. 7QRTCh. 2 - Prob. 8QRTCh. 2 - Prob. 9QRTCh. 2 - Prob. 10QRTCh. 2 - Match these by placing the correct notation in the...Ch. 2 - Prob. 12QRTCh. 2 - Prob. 13QRTCh. 2 - Prob. 14QRTCh. 2 - Prob. 15QRTCh. 2 - Prob. 16QRTCh. 2 - Prob. 17QRTCh. 2 - Prob. 18QRTCh. 2 - Prob. 19QRTCh. 2 - Prob. 20QRTCh. 2 - Prob. 21QRTCh. 2 - Prob. 22QRTCh. 2 - Prob. 23QRTCh. 2 - Prob. 24QRTCh. 2 - Prob. 25QRTCh. 2 - Prob. 26QRTCh. 2 - Prob. 27QRTCh. 2 - Prob. 28QRTCh. 2 - Argon has three naturally occurring isotopes:...Ch. 2 - Prob. 30QRTCh. 2 - Prob. 31QRTCh. 2 - Prob. 32QRTCh. 2 - Prob. 33QRTCh. 2 - Prob. 34QRTCh. 2 - Prob. 35QRTCh. 2 - Prob. 36QRTCh. 2 - Prob. 37QRTCh. 2 - Prob. 38QRTCh. 2 - Prob. 39QRTCh. 2 - Prob. 40QRTCh. 2 - Prob. 41QRTCh. 2 - Prob. 42QRTCh. 2 - Prob. 43QRTCh. 2 - Prob. 44QRTCh. 2 - Prob. 45QRTCh. 2 - Prob. 46QRTCh. 2 - Prob. 47QRTCh. 2 - Prob. 48QRTCh. 2 - Prob. 49QRTCh. 2 - Prob. 50QRTCh. 2 - Prob. 51QRTCh. 2 - Prob. 52QRTCh. 2 - Prob. 53QRTCh. 2 - Prob. 54QRTCh. 2 - Prob. 55QRTCh. 2 - Prob. 56QRTCh. 2 - Prob. 57QRTCh. 2 - Prob. 58QRTCh. 2 - Prob. 59QRTCh. 2 - Prob. 60QRTCh. 2 - Prob. 61QRTCh. 2 - Prob. 62QRTCh. 2 - Prob. 63QRTCh. 2 - Prob. 64QRTCh. 2 - Prob. 65QRTCh. 2 - Prob. 66QRTCh. 2 - Prob. 67QRTCh. 2 - Prob. 68QRTCh. 2 - Prob. 69QRTCh. 2 - Prob. 70QRTCh. 2 - Prob. 71QRTCh. 2 - Prob. 72QRTCh. 2 - Prob. 73QRTCh. 2 - Prob. 74QRTCh. 2 - If you have a ring that contains 1.94 g gold,...Ch. 2 - You have a pure sample of the antiseptic...Ch. 2 - You have a pure sample of apholate, C12H24N9P3, a...Ch. 2 - Prob. 78QRTCh. 2 - Prob. 79QRTCh. 2 - Prob. 80QRTCh. 2 - Prob. 81QRTCh. 2 - Prob. 82QRTCh. 2 - Prob. 83QRTCh. 2 - Prob. 84QRTCh. 2 - Prob. 85QRTCh. 2 - Prob. 86QRTCh. 2 - Prob. 87QRTCh. 2 - Prob. 88QRTCh. 2 - Prob. 89QRTCh. 2 - Prob. 90QRTCh. 2 - Quinine (molar mass = 324.41 g/mol) is used as a...Ch. 2 - Prob. 92QRTCh. 2 - The mineral uraninite is a uranium oxide that is...Ch. 2 - Carbonic anhydrase, an important enzyme in...Ch. 2 - Nitrogen fixation in the root nodules of peas and...Ch. 2 - Disilane, Si2Hx, contains 90.28% silicon by mass....Ch. 2 - Chalky, white crystals in mineral collections are...Ch. 2 - A well-known reagent in analytical chemistry,...Ch. 2 - Prob. 99QRTCh. 2 - Prob. 100QRTCh. 2 - The density of a solution of sulfuric acid is...Ch. 2 - Prob. 102QRTCh. 2 - Prob. 103QRTCh. 2 - Prob. 104QRTCh. 2 - Prob. 105QRTCh. 2 - Prob. 106QRTCh. 2 - Prob. 107QRTCh. 2 - The Statue of Liberty in New York harbor is made...Ch. 2 - Prob. 109QRTCh. 2 - Prob. 110QRTCh. 2 - Prob. 111QRTCh. 2 - Prob. 112QRTCh. 2 - Prob. 113QRTCh. 2 - Prob. 114QRTCh. 2 - Prob. 115QRTCh. 2 - Prob. 116QRTCh. 2 - Prob. 117QRTCh. 2 - Prob. 118QRTCh. 2 - Prob. 119QRTCh. 2 - Prob. 120QRTCh. 2 - Prob. 121QRTCh. 2 - Prob. 122QRTCh. 2 - Prob. 123QRTCh. 2 - Prob. 124QRTCh. 2 - Prob. 125QRTCh. 2 - Prob. 126QRTCh. 2 - Prob. 127QRTCh. 2 - Prob. 128QRTCh. 2 - Prob. 129QRTCh. 2 - The element bromine is Br2, so the mass of a Br2...Ch. 2 - Uranium is used as a fuel, primarily in the form...Ch. 2 - Prob. 132QRTCh. 2 - Hemoglobin is an iron-containing protein (molar...Ch. 2 - There are three naturally occurring isotopes of...Ch. 2 - Prob. 135QRTCh. 2 - Prob. 136QRTCh. 2 - Prob. 137QRTCh. 2 - An adult human body contains 6.0 L blood, which...Ch. 2 - Prob. 139QRTCh. 2 - Prob. 140QRTCh. 2 - Prob. 141QRTCh. 2 - The present average concentration (mass percent)...Ch. 2 - Prob. 144QRTCh. 2 - A 4.22-g mixture of calcium chloride and sodium...Ch. 2 - A certain metal, M, forms two oxides, M2O and MO....Ch. 2 - If you heat Al with an element from Group 6A, an...Ch. 2 - Prob. 2.ACPCh. 2 - The age of the universe is unknown, but some...Ch. 2 - Prob. 2.CCPCh. 2 - Prob. 2.DCPCh. 2 - Prob. 2.ECP
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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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