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OWLv2 with LabSkills for Gilbert/Martin's Experimental Organic Chemistry: A Miniscale & Microscale Approach, 6th Edition, [Instant Access], 4 terms (24 months)
6th Edition
ISBN: 9781305387676
Author: John C. Gilbert; Stephen F. Martin
Publisher: Cengage Learning US
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Question
Chapter 5.4, Problem 9E
Interpretation Introduction
Interpretation: The reason of performing a simple distillation needs to be determined from the given options.
Concept Introduction: Solvent extraction method is also called as liquid-liquid extraction. It is the method that is used to separate compounds on the basis of their relative solubility in two different immiscible solvents.
Here, the immiscible solvents cannot get mixed up together therefore they make two separate layers. In the extraction of a solute from one liquid, another immiscible solvent must be used. Usually water is used with certain organic solvent as organic solvent and water are immiscible into each other. At equilibrium the ratio of concentration of solute is constant in each layer that can be represented by partition coefficient or distribution coefficient. It is the ratio of the concentration of a substance in one medium (C1) to the concentration in a second medium (C2) at equilibrium.
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20. The Brusselator. This hypothetical system was first proposed by a group work-
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scribing a Brusselator are:
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Problem 3. Provide a mechanism for the following transformation:
H₂SO A
Me.
Me
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xi
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2. H₂O
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Draw the missing reagent X you think will make this synthesis work in the drawing area below.
If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank.
Click and drag to start drawing a
structure.
There is no reagent that will make this synthesis work without complications.
: ☐
S
☐
Chapter 5 Solutions
OWLv2 with LabSkills for Gilbert/Martin's Experimental Organic Chemistry: A Miniscale & Microscale Approach, 6th Edition, [Instant Access], 4 terms (24 months)
Ch. 5.3 - Prob. 1ECh. 5.3 - Prob. 2ECh. 5.3 - Prob. 3ECh. 5.3 - Prob. 4ECh. 5.3 - Prob. 5ECh. 5.3 - Prob. 6ECh. 5.3 - Prob. 7ECh. 5.3 - Prob. 8ECh. 5.3 - Prob. 9ECh. 5.3 - Prob. 10E
Ch. 5.3 - Prob. 11ECh. 5.3 - Prob. 12ECh. 5.3 - Prob. 13ECh. 5.3 - Prob. 14ECh. 5.3 - Prob. 15ECh. 5.3 - Prob. 16ECh. 5.3 - Prob. 17ECh. 5.3 - Prob. 18ECh. 5.3 - Prob. 19ECh. 5.3 - Prob. 20ECh. 5.3 - Prob. 21ECh. 5.3 - Prob. 22ECh. 5.4 - Prob. 1ECh. 5.4 - Prob. 2ECh. 5.4 - Prob. 3ECh. 5.4 - Prob. 4ECh. 5.4 - Prob. 5ECh. 5.4 - Prob. 6ECh. 5.4 - Prob. 7ECh. 5.4 - Prob. 8ECh. 5.4 - Prob. 9ECh. 5.4 - Prob. 10ECh. 5.4 - Prob. 11ECh. 5.4 - Prob. 12E
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