Organic Chemistry 3rd.ed. Klein Evaluation/desk Copy
3rd Edition
ISBN: 9781119320524
Author: Klein
Publisher: WILEY
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Chapter 20, Problem 93CP
Interpretation Introduction
Interpretation: For the given transformation, a plausible mechanism has to be proposed.
Concept Introduction:
For any given transformation, the following mandatory observations have to be made clear to predict the synthetic scheme:
- Observe whether there is any change in the carbon skeleton.
- Observe whether there is any change in the location of the
functional group . - Predict the synthetic scheme in such a way that these two observations have to be achieved within the minimum chemo selective steps.
The given transformation is:
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Consider this organic reaction:
...
OH
CI
Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significant
rate, check the box under the drawing area instead.
☐ No Reaction.
Click and drag to start drawing a structure.
:
а
Consider the following reactants:
Br
Would elimination take place at a significant rate between these reactants?
Note for advanced students: by significant, we mean that the rate of elimination
would be greater than the rate of competing substitution reactions.
yes
O no
If you said elimination would take place, draw the major products in the upper
drawing area.
If you said elimination would take place, also draw the complete mechanism for one
of the major products in the lower drawing area.
If there is more than one major product, you may draw the mechanism that leads to
any of them.
Major Products:
Draw one product of an elimination reaction between the molecules below.
Note: There may be several correct answers. You only need to draw one of them. You do not need to draw any of the side products of the reaction.
OH
+
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: ☐
+
Х
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Chapter 20 Solutions
Organic Chemistry 3rd.ed. Klein Evaluation/desk Copy
Ch. 20.2 - Prob. 1CCCh. 20.2 - Prob. 2CCCh. 20.2 - Prob. 3CCCh. 20.3 - Prob. 4CCCh. 20.3 - Prob. 5CCCh. 20.3 - Prob. 6CCCh. 20.3 - Prob. 7CCCh. 20.3 - Prob. 8CCCh. 20.3 - Prob. 9CCCh. 20.4 - Prob. 10CC
Ch. 20.5 - Prob. 11CCCh. 20.6 - Prob. 12CCCh. 20.6 - Prob. 13CCCh. 20.7 - Prob. 1LTSCh. 20.7 - Prob. 14PTSCh. 20.7 - Prob. 15ATSCh. 20.8 - Prob. 16CCCh. 20.8 - Prob. 17CCCh. 20.8 - Prob. 18CCCh. 20.9 - Prob. 19CCCh. 20.10 - Prob. 20CCCh. 20.10 - Prob. 21CCCh. 20.11 - Prob. 22CCCh. 20.11 - Prob. 23CCCh. 20.12 - Prob. 24CCCh. 20.12 - Prob. 25CCCh. 20.12 - Prob. 26CCCh. 20.13 - Prob. 27CCCh. 20.13 - Prob. 28CCCh. 20.13 - Prob. 29CCCh. 20.14 - Prob. 2LTSCh. 20.14 - Prob. 30PTSCh. 20.14 - Prob. 31ATSCh. 20.14 - Prob. 3LTSCh. 20.14 - Prob. 32PTSCh. 20.14 - Prob. 33ATSCh. 20.15 - Prob. 34CCCh. 20 - Prob. 35PPCh. 20 - Prob. 36PPCh. 20 - Prob. 37PPCh. 20 - Prob. 38PPCh. 20 - Prob. 39PPCh. 20 - Prob. 40PPCh. 20 - Prob. 41PPCh. 20 - Prob. 42PPCh. 20 - Prob. 43PPCh. 20 - Prob. 44PPCh. 20 - Prob. 45PPCh. 20 - Prob. 46PPCh. 20 - Prob. 47PPCh. 20 - Prob. 48PPCh. 20 - Prob. 49PPCh. 20 - Prob. 50PPCh. 20 - Prob. 51PPCh. 20 - Prob. 52PPCh. 20 - Prob. 53PPCh. 20 - Prob. 54PPCh. 20 - Prob. 55PPCh. 20 - Prob. 56PPCh. 20 - Prob. 57PPCh. 20 - Prob. 58PPCh. 20 - Prob. 59PPCh. 20 - Prob. 60PPCh. 20 - Prob. 61PPCh. 20 - Prob. 62PPCh. 20 - Prob. 63PPCh. 20 - Prob. 64PPCh. 20 - Prob. 65PPCh. 20 - Prob. 66PPCh. 20 - Prob. 67PPCh. 20 - Prob. 68PPCh. 20 - Prob. 69PPCh. 20 - Prob. 70IPCh. 20 - Prob. 72IPCh. 20 - Prob. 73IPCh. 20 - Prob. 74IPCh. 20 - Prob. 75IPCh. 20 - Prob. 76IPCh. 20 - Prob. 77IPCh. 20 - Prob. 78IPCh. 20 - Prob. 79IPCh. 20 - Prob. 80IPCh. 20 - Prob. 81IPCh. 20 - Prob. 82IPCh. 20 - Prob. 83IPCh. 20 - Prob. 84IPCh. 20 - Compound 3 (below) was used as an intermediate in...Ch. 20 - The m- and p-substituted methyl benzoates listed...Ch. 20 - Prob. 87IPCh. 20 - Prob. 88IPCh. 20 - Prob. 89IPCh. 20 - Prob. 90CPCh. 20 - Prob. 91CPCh. 20 - Prob. 92CPCh. 20 - Prob. 93CP
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