Draw Butane's Sawhorse, Wedge, and Newman projections and show/discuss their plane of symmety or center of symmetry or axis of symetry.
Draw Butane's Sawhorse, Wedge, and Newman projections and show/discuss their plane of symmety or center of...
Describe the Sawhorse, Wedge, and Newman projections plane and axis of symmetry of Ethane's eclipsed conformation viewed along the C1-C2 axis
Draw Propane's Sawhorse, Wedge, and Newman projections.
Draw Ethane's Sawhorse, Wedge, and Newman projections.
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.
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.
Draw theSawhorsee and newman projections of trans 1,3 dibromo cyclohexane in chair form. Please include how you went from chair formation to sawhorse formation and then to new projection
(a) Draw the saw-horse (or wedge-dash) projection of (2S,3R)-3-methylpentan-2-ol. [Marks: 1] (b) Draw the Newman projections of the 2-3 bond in (2S,3R)-3-methylpentan-2-ol. [Marks: 2] (c) Based on the Newman projections from part b. - draw a rotation vs. energy diagram (you do NOT need to give specific energy values in this diagram) that will allow you to identify the most stable confirmation around the 2-3 bond. Assume the greatest steric and torsional strain occurs when the hydroxyl and ethyl groups...
Part B: Newman Projections Newman Projections are used to show a conformation of a molecule. Use 6 different colored atoms or groups of atoms to make a key for the following molecule. Begin by rotating the molecule about the vertical axis so that groups 1-3 come out in the front and groups 4-6 go back behind the page (as shown in the diagram in the next page). KEY COLORED ATOM OR GROUP OF ATOMS 1 2 3 4 5 6...
3. 1) Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this Newman projections as a staggered or eclijpsed conformation. (3) Rotate this Newman projection to draw the Newman projection of the most stable conformation of this compound. (3) Label this Newman projections as a staggered or eclipsed conformation. (4) Re-draw this most stable conformation in a wedge-dash form as the original compound below is shown). a. он в н b. Cl 3. 1)...
using the c3-c4 axis, draw newman projections for an eclipsed and a staggered conformation of 2.5 dimethylhexane. Draw the most stable conformation for the molecule as well.