Organic Chemistry
3rd Edition
ISBN: 9781119338352
Author: Klein
Publisher: WILEY
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Question
Chapter 4.12, Problem 25PTS
(a)
Interpretation Introduction
Interpretation:
The axial and equatorial chair conformation of given compounds are should be drown.
Concept Introduction:
Conformational isomers:
- The two or more compounds have same molecular formula and different structural formulas are called conformational isomers.
- The Cyclohexane s have a chair and boat conformations.
- The chair conformation of Cyclohexane is more stable than boat form.
- The chair conformation of Cyclohexane have two positions to substituents which are axial and equatorial.
- The substituent occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.
- The substituent occupy at similar to a horizontal axis passing through the chair conformation of Cyclohexane ring is called equatorial position.
(b)
Interpretation Introduction
Interpretation:
The axial and equatorial chair conformation of given compounds are should be drown.
Concept Introduction:
Conformational isomers:
- The two or more compounds have same molecular formula and different structural formulas are called conformational isomers.
- The Cyclohexane s have a chair and boat conformations.
- The chair conformation of Cyclohexane is more stable than boat form.
- The chair conformation of Cyclohexane have two positions to substituents which are axial and equatorial.
- The substituent occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.
- The substituent occupy at similar to a horizontal axis passing through the chair conformation of Cyclohexane ring is called equatorial position.
(c)
Interpretation Introduction
Interpretation:
The axial and equatorial chair conformation of given compounds are should be drown.
Concept Introduction:
Conformational isomers:
- The two or more compounds have same molecular formula and different structural formulas are called conformational isomers.
- The Cyclohexane s have a chair and boat conformations.
- The chair conformation of Cyclohexane is more stable than boat form.
- The chair conformation of Cyclohexane have two positions to substituents which are axial and equatorial.
- The substituent occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.
- The substituent occupy at similar to a horizontal axis passing through the chair conformation of Cyclohexane ring is called equatorial position.
(d)
Interpretation Introduction
Interpretation:
The axial and equatorial chair conformation of given compounds are should be drown.
Concept Introduction:
Conformational isomers:
- The two or more compounds have same molecular formula and different structural formulas are called conformational isomers.
- The Cyclohexane s have a chair and boat conformations.
- The chair conformation of Cyclohexane is more stable than boat form.
- The chair conformation of Cyclohexane have two positions to substituents which are axial and equatorial.
- The substituent occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.
- The substituent occupy at similar to a horizontal axis passing through the chair conformation of Cyclohexane ring is called equatorial position.
(e)
Interpretation Introduction
Interpretation:
The axial and equatorial chair conformation of given compounds are should be drown.
Concept Introduction:
Conformational isomers:
- The two or more compounds have same molecular formula and different structural formulas are called conformational isomers.
- The Cyclohexane s have a chair and boat conformations.
- The chair conformation of Cyclohexane is more stable than boat form.
- The chair conformation of Cyclohexane have two positions to substituents which are axial and equatorial.
- The substituent occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.
- The substituent occupy at similar to a horizontal axis passing through the chair conformation of Cyclohexane ring is called equatorial position.
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Organic Chemistry
Ch. 4.2 - Prob. 1LTSCh. 4.2 - Prob. 1PTSCh. 4.2 - Prob. 2PTSCh. 4.2 - Prob. 3ATSCh. 4.2 - Prob. 2LTSCh. 4.2 - Prob. 4PTSCh. 4.2 - Prob. 5ATSCh. 4.2 - Prob. 3LTSCh. 4.2 - Prob. 6PTSCh. 4.2 - Prob. 7ATS
Ch. 4.2 - Prob. 4LTSCh. 4.2 - Prob. 8PTSCh. 4.2 - Prob. 9PTSCh. 4.2 - Prob. 10ATSCh. 4.2 - Prob. 5LTSCh. 4.2 - Prob. 11PTSCh. 4.2 - Prob. 12PTSCh. 4.2 - Prob. 13ATSCh. 4.3 - Prob. 6LTSCh. 4.3 - Prob. 14PTSCh. 4.3 - Prob. 15ATSCh. 4.6 - Prob. 7LTSCh. 4.6 - Prob. 16PTSCh. 4.6 - Prob. 17ATSCh. 4.7 - Prob. 18CCCh. 4.8 - Prob. 8LTSCh. 4.8 - Prob. 19PTSCh. 4.8 - Prob. 20ATSCh. 4.11 - Prob. 9LTSCh. 4.11 - Prob. 21PTSCh. 4.11 - Prob. 22ATSCh. 4.11 - Prob. 10LTSCh. 4.11 - Prob. 23PTSCh. 4.11 - Prob. 24ATSCh. 4.12 - Prob. 11LTSCh. 4.12 - Prob. 25PTSCh. 4.12 - Prob. 26ATSCh. 4.12 - Prob. 27CCCh. 4.13 - Prob. 12LTSCh. 4.13 - Prob. 28PTSCh. 4.13 - Prob. 29ATSCh. 4.13 - Prob. 13LTSCh. 4.13 - Prob. 30PTSCh. 4.13 - Prob. 31ATSCh. 4.13 - Prob. 32ATSCh. 4.14 - Prob. 33CCCh. 4.14 - Prob. 34CCCh. 4.14 - Prob. 35CCCh. 4 - Prob. 36PPCh. 4 - Prob. 37PPCh. 4 - Prob. 38PPCh. 4 - Prob. 39PPCh. 4 - Prob. 40PPCh. 4 - Prob. 41PPCh. 4 - Prob. 42PPCh. 4 - Prob. 43PPCh. 4 - Prob. 44PPCh. 4 - Prob. 45PPCh. 4 - Prob. 46PPCh. 4 - Prob. 47PPCh. 4 - Prob. 48PPCh. 4 - Prob. 49PPCh. 4 - Prob. 50PPCh. 4 - Prob. 51PPCh. 4 - Prob. 52PPCh. 4 - Prob. 53PPCh. 4 - Prob. 54PPCh. 4 - Prob. 55PPCh. 4 - Prob. 56PPCh. 4 - Prob. 57PPCh. 4 - Prob. 58PPCh. 4 - Prob. 59PPCh. 4 - Prob. 60PPCh. 4 - Prob. 61IPCh. 4 - Prob. 62IPCh. 4 - Prob. 64IPCh. 4 - Prob. 65IPCh. 4 - Prob. 66IPCh. 4 - Prob. 67IPCh. 4 - Prob. 68IPCh. 4 - Prob. 69IPCh. 4 - Prob. 70IPCh. 4 -
All of the following are representations of...Ch. 4 - Prob. 72IPCh. 4 -
Which of the following is expected to have the...Ch. 4 - Prob. 74IPCh. 4 - Prob. 75CPCh. 4 -
The all-trans-1,2,3,4,5,6-hexaethylcyclohexane...Ch. 4 -
Compounds 1 and 2 were prepared, and the...
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