Foundations of College Chemistry 15e Binder Ready Version + WileyPLUS Registration Card
15th Edition
ISBN: 9781119231318
Author: Morris Hein
Publisher: Wiley (WileyPLUS Products)
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Chapter 6, Problem 3RQ
Interpretation Introduction
Interpretation:
The fact that two elements combine in
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42. Which of the following halogenated compounds can be used successfully to prepare a Grignard reagent for
alcohol synthesis by subsequent reaction with an aldehyde or ketone? Which ones cannot and why?
H3C CH3
a.
Br
H OH
b.
Cl
C.
I H
H
d. Cl
e.
H
OCH3
Br
H
For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check
the appropriate box.
Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below.
Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions
- just focus on the first stable product you expect to form in solution.
?
Will the first
MgBr
product that forms in this reaction
create a new CC bond?
olo
?
OH
جمله
O Yes
Ⓒ No
MgCl
?
Will the first product that forms in this reaction
create a new CC bond?
Click and drag to start drawing a
structure.
Yes
No
X
☐ :
☐
टे
PH
Assign all the protons
Chapter 6 Solutions
Foundations of College Chemistry 15e Binder Ready Version + WileyPLUS Registration Card
Ch. 6.2 - Prob. 6.1PCh. 6.3 - Prob. 6.2PCh. 6.4 - Prob. 6.3PCh. 6.4 - Prob. 6.4PCh. 6.4 - Prob. 6.5PCh. 6.4 - Prob. 6.6PCh. 6.4 - Prob. 6.7PCh. 6.5 - Prob. 6.8PCh. 6.5 - Prob. 6.9PCh. 6.6 - Prob. 6.10P
Ch. 6.6 - Prob. 6.11PCh. 6 - Prob. 1RQCh. 6 - Prob. 2RQCh. 6 - Prob. 3RQCh. 6 - Prob. 4RQCh. 6 - Prob. 5RQCh. 6 - Prob. 6RQCh. 6 - Prob. 7RQCh. 6 - Prob. 8RQCh. 6 - Prob. 9RQCh. 6 - Prob. 10RQCh. 6 - Prob. 11RQCh. 6 - Prob. 12RQCh. 6 - Prob. 1PECh. 6 - Prob. 2PECh. 6 - Prob. 3PECh. 6 - Prob. 4PECh. 6 - Prob. 5PECh. 6 - Prob. 6PECh. 6 - Prob. 7PECh. 6 - Prob. 8PECh. 6 - Prob. 9PECh. 6 - Prob. 10PECh. 6 - Prob. 11PECh. 6 - Prob. 12PECh. 6 - Prob. 13PECh. 6 - Prob. 14PECh. 6 - Prob. 15PECh. 6 - Prob. 16PECh. 6 - Prob. 17PECh. 6 - Prob. 18PECh. 6 - Prob. 19PECh. 6 - Prob. 20PECh. 6 - Prob. 21PECh. 6 - Prob. 22PECh. 6 - Prob. 23PECh. 6 - Prob. 24PECh. 6 - Prob. 25PECh. 6 - Prob. 26PECh. 6 - Prob. 27PECh. 6 - Prob. 28PECh. 6 - Prob. 29AECh. 6 - Prob. 30AECh. 6 - Prob. 31AECh. 6 - Prob. 32AECh. 6 - Prob. 33AECh. 6 - Prob. 34AECh. 6 - Prob. 35AECh. 6 - Prob. 36AECh. 6 - Prob. 37AECh. 6 - Prob. 38AECh. 6 - Prob. 39AECh. 6 - Prob. 40AECh. 6 - Prob. 41AECh. 6 - Prob. 42AECh. 6 - Prob. 44CE
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- 9 7 8 C 9 8 200 190 B 5 A -197.72 9 8 7 15 4 3 0: ང་ 200 190 180 147.52 134.98 170 160 150 140 130 120 110 100 90 90 OH 10 4 3 1 2 -143.04 140. 180 170 160 150 140 130 120 110 100 90 CI 3 5 1 2 141.89 140.07 200 190 180 170 160 150 140 130 120 110 100 ៖- 90 129. 126.25 80 70 60 -60 50 40 10 125.19 -129.21 80 70 3.0 20 20 -8 60 50 10 ppm -20 40 128.31 80 80 70 60 50 40 40 -70.27 3.0 20 10 ppm 00˚0-- 77.17 30 20 20 -45.36 10 ppm -0.00 26.48 22.32 ―30.10 ―-0.00arrow_forwardAssign all the carbonsarrow_forwardC 5 4 3 CI 2 the Righ B A 5 4 3 The Lich. OH 10 4 5 3 1 LOOP- -147.52 T 77.17 -45.36 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 ppm B -126.25 77.03 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 ppm 200 190 180 170 160 150 140 130 120 110 100 90 80 TO LL <-50.00 70 60 50 40 30 20 10 ppm 45.06 30.18 -26.45 22.36 --0.00 45.07 7.5 1.93 2.05 -30.24 -22.36 C A 7 8 5 ° 4 3 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 ppm 9 8 5 4 3 ཡི་ OH 10 2 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 5 4 3 2 that th 7 I 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 115 2.21 4.00 1.0 ppm 6.96 2.76 5.01 1.0 ppm 6.30 1.00arrow_forward
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- how to get limiting reactant and % yield based off this data Compound Mass 6) Volume(mL Ben zaphone-5008 ne Acetic Acid 1. Sam L 2-propanot 8.00 Benzopin- a col 030445 Benzopin a Colone 0.06743 Results Compound Melting Point (°c) Benzopin acol 172°c - 175.8 °c Benzoping to lone 1797-180.9arrow_forwardAssign ALL signals for the proton and carbon NMR spectra on the following pages.arrow_forward7.5 1.93 2.05 C B A 4 3 5 The Joh. 9 7 8 1 2 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 ppm 9 7 8 0.86 OH 10 4 3 5 1 2 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 ppm 9 7 8 CI 4 3 5 1 2 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 2.21 4.00 1.5 2.00 2.07 1.0 ppm 2.76arrow_forward
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