1: Draw the chain conformer of... 1a. Cyclohexane, label all the axial and equatorial hydrogens 1b. The most stable conformer of ethylcyclohexane 1c. The most sable conformer of trans-1-tert-butyl-3-methylcyclohexane

6. Draw the two chair conformations of the molecule below. Which is the most stable? HO.

Consider 1,2-dimethylcyclohexane. a.Draw structures for the cis and trans isomers using a hexagon for the sixmembered ring. b. Draw the two possible chair conformations for the cis isomer. Which conformation, if either, is more stable? c. Draw the two possible chair conformations for the trans isomer. Which conformation, if either, is more stable? d.Which isomer, cis or trans, is more stable and why?

I need help with Drawing one constitutional isomer of cis-1,2-dichlorocyclopropane with the same size ring.

Draw the following molecules in their most stable conformation. You do not have to draw the least stable conformation, unless you find it helpful practice.

8. Draw all possible monochlorinated derivatives for :(hint: look for primary, secondary and tertiary carbon atoms and associated Hydrogen atoms in each molecule) a) Cyclopentane c) 2-methylpentane b) methyl cyclopentane d) 2,2,3,3-tetramethylbutane

For the following two pairs of molecules, (1) Draw out the chair conformation for each molecule, flip the ring if it is possible. (2) Compare both molecules to circle out which one is more stable. (3) Identify their relationship as: constitutional isomer, conformational isomer, stereoisomer or identical. (4) Find all the chiral center on each molecule and label them. VS. ****

Please don't provide handwriting solutions....

Identify and label all functional groups Identify and label all stereo centers

Explain why please