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Even though the methyl group occupies an equatorial site, the conformation shown is not the most stable one for methylcyclohexane. Explain.
Determine whether the two structures in each of the following pairs represent constitutional isomers, different conformations of the same compound, or stereoisomers that cannot be interconverted by rotation about single ...
Identify the more stable stereoisomer in each of the following pairs, and give the reason for your choice: (a) cis- or trans-1-Isopropyl-2-methylcyclohexane (b) cis- or trans-1-Isopropyl-3-methylcyclohexane (c) cis- or ...
A typical steroid skeleton is shown along with the numbering scheme used for this class of compounds. Specify in each case whether the designated substituent is axial or equatorial.
As noted in Problem 4.7, hydrogen cyanide (HCN) has a pKa of 9.1. Is cyanide ion (CN─) a stronger base or a weaker base than hydroxide ion (HO─)?
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