Draw Newman projections (looking down the C2-C3 bond) of the three staggered conformers of 2-methylbutane. Rank...
Draw Newman projections of 2, 3-dimethylbutane, looking down the C2 to C3 bond, in the most and least stable conformations. Label any important interactions.
can you show how you got the anwser for both set by step Draw Newman projections looking down the C3 to C4 bond of (3R, 4S)-3,4-dibromoheptane Draw Newman projections looking down the C3 to C2 bond of (2R, 3S)-2-fluoro-3-ethylheptane
Sighting along C2-C1 bond of 2-methylpropane and C2-C3 of 2-methylbutane a. Draw a Newman projection of the most stable conformation of each compound b. Draw a Newman projection of the least stable confirmation of each compound
Draw a newman projection of the most stable staggered conformation of 4-bromo-3-methylheptane looking down the C3-C4 bond. Then draw a newman projection of the least stable staggered conformation of the same compound looking down the C3-C4 bond - label where different type(s) of strain occur making this conformation less stable? I have no idea how to do this so step by step would be perfect. Thank you.
3. Consider 2,2,4-trimethylpentane Draw this compound. a. b. Now, provide Newman projections for the three staggered conformations for this compound looking down the C3 - C4 bond. c. Label the orientation of substituents (i.e. gauche or anti) in each structure and circle the most stable conformation(S)
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)...
draw the skeletal formula and newman projections for following: Look down (2 to C3 bond of (28,35, 55)-3,5-dimethylheptan-2-01
Using Newman projections, draw all the staggered and eclipsed conformations that result from rotationaround the indicated bond in 2-methylbutane(shown below) and place these on a graph of energy versus dihedralangle for a 360° rotation about this bond. To orient your graph, one structure has been filled in for you. Please start your conformational analysis and energy curve from this structure.
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.
16. Draw the Newman projection (viewing down the C3-C4 bond) for the two staggered conformations of hexane that have different energies. Indicate the conformation with the lowest energy. (5 pts) 17. Consider the molecule below. (10 pts) CZ Bry Br CI a) Is this molecule chiral? Provide an explanation. b) Draw both chair configurations for this molecule, and circle the more stable conformation (if applicable).