draw the most stable conformation of cyclohexane. why is it strain free
draw the most stable conformation of cyclohexane. why is it strain free
Draw the most stable conformation of the given cyclohexane. Draw
the major product and the mechanism using the cyclohexane you have
drawn.
Draw your answers as line structures and show
stereochemistry of asymmetric centers with wedges and
dashes.
NaOEt ETOH CI
Deposit the most stable confirmation of
hexamethyl-cyclohexane.
Depict the most stable conformation of hexamethyl-cyclohexane in (i) a flat representation of the compound, (ii) a pseudo-3D representation of the compound, and (iii) a Newman projection of the compound.
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters a (axial), elequatorial), d(down), u(up)) next to each substituent to indicate is position in the ring. 1112 COOH
Draw the following substituted cyclohexane in its most stable
chair conformation. Clearly indicate which bonds are axial and
which bonds are equatorial and provide the systematic name for this
compound, using R/S designations to indicate stereochemistry.
CH3 CI CH3 CH3 H3C
Draw the most stable chair conformation for trans-1-chloro-2-isopropylcyclohexane and please explain why its most stable Will Rate Correct Answers!!!!
with explanation
1) Draw a chair conformation of cyclohexane. Then, draw and level properly all axial and equatorial positions on chair form of cyclohexane. 2) Draw chair, half-chair and boat conformations of ethyl cyclohexane and draw an energy diagram to explain their relative stability: 3) Draw two possible chair conformations for each of the mono-substituted cyclohexanes and determine their relative stability with proper explanation. OH 4) Draw two possible chair conformations for each of the di-substituted cyclohexanes and determine their...
3. (10 pts) For each cyclohexane, draw both chair conformations and circle the conformation that is more stable (use the relative size of each substituent to determine which has more 1,3-diaxial strain) S-Bu NH2 t-Bu /25 pts
Cyclohexane: 1.Make a boat conformation. 2.Then a chair conformation In which case are the C-H bonds on neighboring carbons eclipsing the most? 3. In which case do the H atoms on C1 and C4 approach each other most closely? 4. Based on what you saw above, which will be the most stable conformation of cyclohexane? Draw both conformations
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 the most stable chair conformation for the following molecule