Organic Chemistry
Organic Chemistry
3rd Edition
ISBN: 9781119316152
Author: Klein, David R.
Publisher: WILEY
Question
Book Icon
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.

Blurred answer
Students have asked these similar questions
Imagine an electrochemical cell based on these two half reactions with electrolyte concentrations as given below:   Oxidation: Pb(s) → Pb2+(aq, 0.10 M) + 2 e– Reduction: MnO4–(aq, 1.50 M) + 4 H+(aq, 2.0 M) + 3 e– → MnO2(s) + 2 H2O(l) Calculate Ecell (assuming temperature is standard 25 °C).
: ☐ + Draw the Fischer projection of the most common naturally-occurring form of aspartate, with the acid group at the top and the side chain at the bottom. Important: be sure your structure shows the molecule as it would exist at physiological pH. Click and drag to start drawing a structure. ✓
For a silver-silver chloride electrode, the following potentials are observed: E°cell = 0.222 V and E(saturated KCl) = 0.197 V Use this information to find the [Cl–] (technically it’s the activity of Cl– that’s relevant here, but we’ll just call it “concentration” for simplicity) in saturated KCl.

Chapter 4 Solutions

Organic Chemistry

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...
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY