2. a) Draw the most stable chair conformation of cis 1-t-butyl-2-chlorocyclohexane. b) Draw a Newman projection of the best conformation of 4-chlorobut-1-ene looking down the C3-C4 bond.
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- Draw each of the following. (a) Draw a Newman Projection of the following molecule, looking down the C3-C4 bond. Draw C3 in the front. CI Br H (b) Draw a Newman Projection of the most stable and the least stable conformation of the following molecule. Label each H H. CI H CI H5. Draw the most stable chair conformation of the given trisubstituted cyclohexane? BrDraw the most stable conformation of(a) trans-1-tert-butyl-2-methylcyclohexane.
- Draw the most stable chair conformations of each compound and label the substituents as equatorial.a) trans-1-ethyl-3-isopropylcyclohexaneb) cis-1-chloro-4-bromocyclohexanec) 1-fluoro-1-methyl clohexaneWhy is this chair conformation the most stable trans-1-chloro-3-flurocyclohexane? Wouldn't the conformation with Cl & F in equatorial positions be the most stable conformation?- Sight along the C2-C3 bond of butan-2-amine (CH3CH(NH2)CH2CH3), and draw a Newman projection of the (a) second most stable, and the (b) second least stable conformation. - Draw the most stable chair conformation for Bornesitol.
- a.Draw the most stable conformation of trans-1,2-dimethylcyclohexane. b. Draw the most stable conformation of cis-1,2-dimethylcyclohexane.2. a) Draw the most stable chair confomation of: cis 1,3-dichlorocyclohexane b) Draw a Newman projection of the best conformation of 2,3-dimethylpe tane looking down the C2-Ca bond.Draw both cis chair conformations of 2-methylcyclohexanol and circle the more stable one.