Organic Chemistry
2nd Edition
ISBN: 9781118452288
Author: David R. Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Question
Chapter 4.14, Problem 37CC
Interpretation Introduction
Interpretation:
The Haworth projections of cis and trans-1-4-dimethylcyclohexane 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 substituents 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 substituents 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 solutionStudents have asked these similar questions
Question
Suggest a mechanism for the following reactions. Each will require multiple
types of concerted pericyclic reactions (cycloaddition, electrocyclic, and
sigmatropic. Classify each reaction type.
CN
a.
NC
180 °C
Don't used Ai solution and don't used hand raiting
Q2: Ranking Acidity
a) Rank the labeled protons in the following molecule in order of increasing pKa. Briefly
explain the ranking. Use Table 2.2 as reference.
Ha
Нь
HC
H-N
Ha
OHe
b) Atenolol is a drug used to treat high blood pressure. Which of the indicated N-H bonds is
more acidic? Explain. (Hint: use resonance structures to help)
Name the functional groups on atenolol.
H
H-N
atenolol
Ν
H-N
OH Н
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
- Answer d, e, and farrow_forwardIf the rotational constant of a molecule is B = 120 cm-1, it can be stated that the transition from 2←1:a) gives rise to a line at 120 cm-1b) is a forbidden transitionc) gives rise to a line at 240 cm-1d) gives rise to a line at 480 cm-1arrow_forwardBriefly indicate the coordination forms of B and Si in borates and silicates, respectively.arrow_forward
- Can you please draw out the Lewis structure for these two formulasarrow_forwardIn a rotational Raman spectrum of a diatomic molecule it is correct to say that:a) anti-Stokes lines occur at frequencies higher than the excitatory oneb) Stokes lines occur at frequencies higher than the excitatory onec) Rayleigh scattering is not observedd) Rayleigh scattering corresponds to delta J = 0arrow_forwardOf the molecules: H2, N2, HCl, CO2, indicate which ones can give Raman vibration-rotation spectra:a) H2, N2 and HClb) H2, N2, HCl and CO2c) H2 and N2d) all of themarrow_forward
- Can you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forwardCan you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forwardCan you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forward
- Can you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forwardPlease draw and explainarrow_forwardDescribe each highlighted bond in terms of the overlap of atomic orbitals. (a) Н Н H H [References] HIC H H C H H-C-CC-N: H σ character n character (b) HIC H H H H-C-C-C HIC H Н H O-H σ character n character Submit Answer Try Another Version 3 item attempts remainingarrow_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