Discuss the Energy/Angle Strain and Stability based on the table below of Sawhorse, Wedge, and Newman projections of Ethane's eclipsed conformation viewed along the C1-C2 axis.
Eclipsed form of any molecule is less stable than that of staggered form due to a lot of angle strain , we are asked for energies of eclipsed forms here. This question is explained on the basis of given data as follows:
Discuss the Energy/Angle Strain and Stability based on the table below of Sawhorse, Wedge, and Newman...
Describe the Sawhorse, Wedge, and Newman projections plane and axis of symmetry of Ethane's eclipsed conformation viewed along the C1-C2 axis
Draw Butane's Sawhorse, Wedge, and Newman projections and show/discuss their plane of symmety or center of symmetry or axis of symetry.
3. Draw butane in wedge and dash depiction, sawhorse depiction and in its Newman projection looking down the 2.3 bond. Show eclipsed, gauche and anti forms. 4. Draw all Newman projections of 2-methylhexane showing eclipsed, gauche and anti forms. Rotate about the 3.4 carbon-carbon bond and watch what happens to the Draw a potential energy diagram for the rotation about the 3,4 carbon- carbon bond plotting Potential Energy versus Torsion Angle.
For CH3CH2CH3 Propane molecule hold one end of the molecule, take a look down at the C1-C2 axis as you rotate the remaining CH group. Discuss the Energy/Angle Strain and Stability based on the table below for Newman Projections of all of the different conformations of Propane.
3. (a) A bond-line (dash/wedge) structure for butane is shown below. Using the Newman projection templates provided, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the bond indicated. Provide a brie explanation to justify the conformer shown for cach case. (2pts each correct Newman, 2pts for valid explanation) sight down CG- bond Lowest Energy (most stable) Highest Energy (least stable) Explain: (b) For the bond-line structure below...
pt iso 5. (a) For each of the molecules below, draw a Newman projection of the conformation shown. Label any gauche interactions (i) (ii) OH B (b) Draw the Newman projections of the most and least stable conformationns of 3- methylpentane, viewed along the C-C, bond. Label any gauche interactions. example of steric strain or torsional strain? (c) Is a gauche interaction an-
pt iso 5. (a) For each of the molecules below, draw a Newman projection of the conformation...
1. Below is a sawhorse representation of 1-chloro-1-fluoropropane. Construct an energy diagram describing rotation about the C1-C2 bond (shown in red). Draw Newman projections for the 6 limiting conformations. Remember, the larger the substituent, the repulsion between it and other groups. Here, the size increases in the order H F < Cl CH3 more CH3 H H H CI
x Consider 2,2,3-trimethylbuttane. Using a Newman projection formula, draw the most stable conformation, sighting along the C2-C3 bond. Compute the total strain energy for this conformation. Refer to strain energy values given below. Strain energies with respect to atoms/groups bonded to C-C (one atom/group bonded to each C) H <---> H eclipsed: 4 kJ/mol CH3 <---> H eclipsed: 6 kJ/mol CH3 <----> CH3 eclipsed: 11 kJ/mol CH3 <----> CH3 gauche staggered: 3.8 kJ/mol Selected Answer: D. 7.6 kJ/mol Answers: A....
9.78 The two lowest energy conformations of pentane are the anti-anti and the anti-gauche forms, in terms of arrangements around the two central C─C bonds. A recent study analyzed the conformations of 3-heptyne as an “elongated” analogue of pentane, where a carbon-carbon triple bond is “inserted” between C2 and C3 of pentane.[15] Interestingly, the researchers found that in each of the two most stable conformations of 3-heptyne, C1 and C6 are nearly eclipsed (looking down the alkyne group). In one...
10. a. Draw the Newman projections for the dihedral angles listed below for 2-methylpentane if you sight down the 2-3 carbon bond (Assume that the least stable conformation corresponds to the 0° dihedral angle and assume that all rotations are counter clockwise) Using the energy values provided below calculate the total strain energy for each of the listed conformations. b. vii. 0 vili. 60° ix. 120 x. 180° xi. 240 xii. 300°