ball & stick labels Name the above compound, identify each substitutent as axial or equatorial, and tell whether the conformation shown is the more stable or less stable form. Omit customary italics from your name. Substitutents R1 and R2 are designated in the order they appear in the IUPAC name. Axial/equatorial strain energy increments are available in the table below. 1. The IUPAC name is 2. Position of R1 3. The conformation shown is the Position of R2

ball & stick labels Name the above compound, identify each substitutent as axial or equatorial, and tell whether the conformation shown is the more stable or less stable form. Omit customary italics from your name. Substitutents R1 and R2 are designated in the order they appear in the IUPAC name. Axial/equatorial strain energy increments are available in the table below. 1. The IUPAC name is 2. Position of R1 3. The conformation shown is the Position of R2

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Complete the question on paper and snap a photo and upload it as your submission in jpg or pdf format. CI IO H OH a. Generate a Newman projection of the molecule shown above. The red arrow indicated the direction from which your eyes are looking at the molecule. b. Also draw a Newman projection of a conformation that is less stable than the one that you have draw in a. There may be more than one correct option to generate a less stable Newman projection - you need only generate one. You can rotate around the C-C single bond to go between eclipsed and/or staggered conformations. c. Describe why the conformation in b. is less stable than a (name the interactions that make the conformation less stable). Point out where on your structure those interactions are (circling is fine).
Question 11 of 17 > Macmillan Learning Given the planar trisubstituted cyclohexane, fill in the missing substituents (with H, Cl or Br) to complete the two possible cyclohexane chair conformations. Then, determine the more stable conformer. You might find it helpful to make a model of the cyclohexane to help visualize the chair conformations. CI Br H H H H H Chair 1 Which is the more stable conformer? Chair 2 Chair 1 H H chair flip H H H H Answer Bank Chair 2 H Br
HI!!!!! 0° H €2H Looking at C1 with C2 behind C1, complete the Newman Projection diagrams. The angles are defined as the dihedral angle between C1-1 and C2-1. 60° H 120° 180° Complete the following potential energy diagram by plotting relative energy of each of the above Newman Projections is versus dihedral angle. The plot should show the correct relative order of the potential energy of each conformation.
2. Draw Newman projections (= 60° increments) of the conformations of 2R-bromobutane from C2-C3. Indicate anti, gauche and eclipsed conformations. Indicate the most and least stable conformations.
Which is the most stable conformation of the following given trisubsituted cyclohexane?
Assume that you have a variety of cyclohexanes substituted in the positions indicated. Identify the substituents as either axial or equatorial. For example, a 1,2-cis relationship means that one substituent must be axial and one equatorial, whereas a 1,2-trans relationship means that either both substituents are axial or both are equatorial. a) 1,4-cis-disubstituted b) 1,6-cis-disubstituted c) 1,2-cis-disubstituted Submit Answer Try Another Version 6 item attempts remaining optioins fill please both axial only both equatorial only both axial or both equatorial one axial-one equatorial
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Draw the most stable conformation for each of the following substituted cyclohexanes. Show all conformation in Newman projections. Fill in hydrogens to indicate unsubstituted carbons.