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.
Draw a newman projection of the most stable staggered conformation of 4-bromo-3-methylheptane looking down the C3-C4...
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman projection for least stable conformation conformation 2. Draw the Newman projections for butane looking down the C2-C3 bond through a full 360 degree rotation. Start with the anti-staggered Newman projection then draw and label each Newman projection (staggered, eclipsed, gauche, anti-staggered, fully-eclipsed) for every 60 degrees of rotation Newman projection for most stable Newman projection for second-most stable conformation Conformation Newman projection for least...
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)...
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).
that represents the most and the least stable conformation of 3,3- 3) Draw the Newman projection the dimethylhexane viewed along the C3-C4 bond. (3pts)
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.
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)
6) (10 Pts) Draw the most stable and the least stable Newman projection for the following molecule looking down the indicated bond. Most Stable Least Stable 7) (16 Pts) Draw the most stable and the least stable chair form for the molecule below. You must also draw the Newman projection for both chair conformations looking from the direction indicated by the arrows. More stable chair Newman Projection -more stable chair less stable chair Newman Projection -less stable chair 6) (10...
please help!! pe 4 16) Which of the following is the staggered conformation for rotation about the C1-C2 bond in the following structure? Ca-c rtely loocig eciear CH CH,CHCH CH 1 234 L ст, свсн, гV. H 3 H H H IL Ci CHCH V. CHe CH,T CHh 17) Draw the Newman projection that represcnts the most stable conformation of 3,3-dimethylhexane viewed along the C3-C4 bond. 18) Draw the Newman projection that represents the least stable conformation of 3,3-dimethylhexane viewed...
From the perspective of viewing down the C2-C3 bond, draw the Newman projection of the least stable conformation of 2,3-dimethylbutane.
ich Newman projection represents the most stable conformation of 3- methylpentane when viewed down the C2-C3 bond? 0. Wh CH3 13C CH2CH3 H3C CH2CH3 H2C CH2CH3 H3C CH2CH3 CH3 CH3 H3C 4 A. 1 B. 2 C. 3 D. 4 11. What is the IUPAC name of the following compound?