- Use the wedge/hash bond tools to indicate stereochemistry where it exists. - Do not draw wedged or hashed on rings with only one substituent. - Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. - Separate structuros with + signs from the drop-down menu.
- Use the wedge/hash bond tools to indicate stereochemistry where it exists. - Include \( \mathrm{H} \) atoms at chiral centers only. - In cases where there is more than one answer, just draw one. - Do not include lone pairs in your answer. They will not be considered in the grading.
There are four cls, trans isomers for 3-isopropyl-4-methylcyciohexanol, where the cis, trans designations of the substituents are made relative to the on group: - up, up, up (cis,cis) - up, up, down (cis,trans) - up, down, down (trans,ds) - up, down, up (trans,trans) Consider the most stable chair for each of these isomers, and then draw the most stable and least stable isomer based on a comparison of the best chair for cach one. - To simplify matters, consider only axial ys equatorial energies of the groups (li.e. do not worty about the interections between the groups, which in reality is also important). - Use the wedge/hash bond tools to indicate stereochemistry where if exists. - You do not have to explicitly draw \( H \) atoms. - Use "flat" representations of rings, not chairs, in your drawing.