Foundations of College Chemistry, Binder Ready Version
15th Edition
ISBN: 9781119083900
Author: Morris Hein, Susan Arena, Cary Willard
Publisher: WILEY
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Chapter 17, Problem 17RQ
Interpretation Introduction
Interpretation:
Major distinction between reactions that occur in
Concept Introduction:
Devices capable to either produce
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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**
11:14
...
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
5
О
δα
HO-
H
-Br
δα
HO--
+
+
-Br
[B]
8+
HO-
-Br
δα
न
Chapter 17 Solutions
Foundations of College Chemistry, Binder Ready Version
Ch. 17.1 - Prob. 17.1PCh. 17.1 - Prob. 17.2PCh. 17.1 - Prob. 17.3PCh. 17.1 - Prob. 17.4PCh. 17.2 - Prob. 17.5PCh. 17.3 - Prob. 17.6PCh. 17.3 - Prob. 17.7PCh. 17.4 - Prob. 17.8PCh. 17.5 - Prob. 17.9PCh. 17 - Prob. 1RQ
Ch. 17 - Prob. 2RQCh. 17 - Prob. 3RQCh. 17 - Prob. 4RQCh. 17 - Prob. 5RQCh. 17 - Prob. 6RQCh. 17 - Prob. 7RQCh. 17 - Prob. 8RQCh. 17 - Prob. 9RQCh. 17 - Prob. 10RQCh. 17 - Prob. 12RQCh. 17 - Prob. 13RQCh. 17 - Prob. 14RQCh. 17 - Prob. 15RQCh. 17 - Prob. 16RQCh. 17 - Prob. 17RQCh. 17 - Prob. 18RQCh. 17 - Prob. 19RQCh. 17 - Prob. 20RQCh. 17 - Prob. 21RQCh. 17 - Prob. 22RQCh. 17 - Prob. 23RQCh. 17 - Prob. 24RQCh. 17 - Prob. 25RQCh. 17 - Prob. 1PECh. 17 - Prob. 2PECh. 17 - Prob. 3PECh. 17 - Prob. 4PECh. 17 - Prob. 5PECh. 17 - Prob. 6PECh. 17 - Prob. 7PECh. 17 - Prob. 8PECh. 17 - Prob. 9PECh. 17 - Prob. 10PECh. 17 - Prob. 11PECh. 17 - Prob. 12PECh. 17 - Prob. 13PECh. 17 - Prob. 14PECh. 17 - Prob. 15PECh. 17 - Prob. 16PECh. 17 - Prob. 17PECh. 17 - Prob. 18PECh. 17 - Prob. 19PECh. 17 - Prob. 20PECh. 17 - Prob. 21AECh. 17 - Prob. 22AECh. 17 - Prob. 23AECh. 17 - Prob. 24AECh. 17 - Prob. 25AECh. 17 - Prob. 26AECh. 17 - Prob. 27AECh. 17 - Prob. 28AECh. 17 - Prob. 29AECh. 17 - Prob. 30AECh. 17 - Prob. 31AECh. 17 - Prob. 32AECh. 17 - Prob. 33AECh. 17 - Prob. 34AECh. 17 - Prob. 35AECh. 17 - Prob. 36AECh. 17 - Prob. 37AECh. 17 - Prob. 38AECh. 17 - Prob. 39AECh. 17 - Prob. 40AECh. 17 - Prob. 41AECh. 17 - Prob. 42AECh. 17 - Prob. 43AECh. 17 - Prob. 44AECh. 17 - Prob. 45AECh. 17 - Prob. 46AECh. 17 - Prob. 47AECh. 17 - Prob. 48AECh. 17 - Prob. 49AECh. 17 - Prob. 50CECh. 17 - Prob. 51CECh. 17 - Prob. 52CECh. 17 - Prob. 53CE
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- 1/2 - 51% + » GAY Organic Reactions Assignment /26 Write the type of reaction that is occurring on the line provided then complete the reaction. Only include the major products and any byproducts (e.g. H₂O) but no minor products. Please use either full structural diagrams or the combination method shown in the lesson. Skeletal/line diagrams will not be accepted. H3C 1. 2. CH3 A Acid OH Type of Reaction: NH Type of Reaction: + H₂O Catalyst + HBr 3. Type of Reaction: H3C 4. Type Reaction: 5. H3C CH2 + H2O OH + [0] CH3 Type of Reaction: 6. OH CH3 HO CH3 + Type of Reaction: 7. Type of Reaction: + [H]arrow_forwardhumbnai Concentration Terms[1].pdf ox + New Home Edit Sign in Comment Convert Page Fill & Sign Protect Tools Batch +WPS A Free Trial Share Inter Concreting Concentration forms. Hydrogen peroxide is a powerful oxidizing agent wed in concentrated solution in rocket fuels and in dilute solution as a hair bleach. An aqueous sulation of H2O2 is 30% by mass and has density of #liligime calculat the Ⓒmolality ⑥mole fraction of molarity. 20 9. B. A sample of Commercial Concentrated hydrochloric ETarrow_forwardIf a reaction occurs, what would be the major products? Please include a detailed explanation as well as a drawing showing how the reaction occurs and what the final product is.arrow_forward
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