
Organic Chemistry
2nd Edition
ISBN: 9781118452288
Author: David R. Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Question
Chapter 4.14, Problem 38CC
Interpretation Introduction
Interpretation:
The Haworth projections of cis and trans-1,3-ditert-butylcyclohexane are drawn and its stability should be comparatively explained.
Concept Introduction:
Haworth projection:
- The representation of cyclic chemical compounds by normal ring structure and the substituent’s can either pointing up or down on this ring is called Haworth projection.
Conformational isomers:
- The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.
- The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.
- The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.
- The substituent’s are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
From the given compound, choose the proton that best fits each given description.
a
CH2
CH 2
Cl
b
с
CH2
F
Most shielded:
(Choose one)
Least shielded:
(Choose one)
Highest chemical shift:
(Choose one)
Lowest chemical shift:
(Choose one)
×
Consider this molecule:
How many H atoms are in this molecule?
How many different signals could be found in its 1H NMR spectrum?
Note: A multiplet is considered one signal.
For each of the given mass spectrum data, identify whether the compound contains chlorine, bromine, or neither.
Compound
m/z of M* peak
m/z of M
+ 2 peak
ratio of M+ : M
+ 2 peak
Which element is present?
A
122
no M
+ 2 peak
not applicable
(Choose one)
B
78
80
3:1
(Choose one)
C
227
229
1:1
(Choose one)
Chapter 4 Solutions
Organic Chemistry
Ch. 4.2 - Prob. 1LTSCh. 4.2 - Prob. 1PTSCh. 4.2 - Prob. 2ATSCh. 4.2 - Prob. 3ATSCh. 4.2 - Prob. 4ATSCh. 4.2 - Prob. 2LTSCh. 4.2 - Prob. 5PTSCh. 4.2 - Prob. 6ATSCh. 4.2 - Prob. 3LTSCh. 4.2 - Prob. 7PTS
Ch. 4.2 - Prob. 8ATSCh. 4.2 - Prob. 9ATSCh. 4.2 - Prob. 4LTSCh. 4.2 - Prob. 10PTSCh. 4.2 - Prob. 11ATSCh. 4.2 - Prob. 5LTSCh. 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. 4.6 - Prob. 18ATSCh. 4.7 - Prob. 19CCCh. 4.8 - Prob. 8LTSCh. 4.8 - Prob. 20PTSCh. 4.8 - Prob. 21ATSCh. 4.11 - Prob. 9LTSCh. 4.11 - Prob. 22PTSCh. 4.11 - Prob. 23ATSCh. 4.11 - Prob. 10LTSCh. 4.11 - Prob. 24PTSCh. 4.11 - Prob. 25PTSCh. 4.11 - Prob. 26PTSCh. 4.11 - Prob. 27ATSCh. 4.12 - Prob. 11LTSCh. 4.12 - Prob. 28PTSCh. 4.12 - Prob. 29ATSCh. 4.12 - Prob. 30CCCh. 4.12 - Prob. 12LTSCh. 4.12 - Prob. 31PTSCh. 4.12 - Prob. 32ATSCh. 4.12 - Prob. 13LTSCh. 4.12 - Prob. 33PTSCh. 4.12 - Prob. 34ATSCh. 4.12 - Prob. 35ATSCh. 4.14 - Prob. 36CCCh. 4.14 - Prob. 37CCCh. 4.14 - Prob. 38CCCh. 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. 61PPCh. 4 - Prob. 62PPCh. 4 - Prob. 63PPCh. 4 - Prob. 64IPCh. 4 - Prob. 65IPCh. 4 - Prob. 67IPCh. 4 - Prob. 68IPCh. 4 - Prob. 69IP
Knowledge Booster
Similar questions
- Don't used hand raiting and don't used Ai solutionarrow_forward2' P17E.6 The oxidation of NO to NO 2 2 NO(g) + O2(g) → 2NO2(g), proceeds by the following mechanism: NO + NO → N₂O₂ k₁ N2O2 NO NO K = N2O2 + O2 → NO2 + NO₂ Ко Verify that application of the steady-state approximation to the intermediate N2O2 results in the rate law d[NO₂] _ 2kk₁[NO][O₂] = dt k+k₁₂[O₂]arrow_forwardPLEASE ANSWER BOTH i) and ii) !!!!arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY