CHE 230-002

Facts and Skills to Master for the Second Exam

The second exam will cover Chapters 1-5 in Jones. The following guidelines are not meant to be complete or comprehensive lists of the information you are expected to know.

You are expected to have command of all the material covered on the first exam.

You should be able to determine which among a set of compounds is most acidic or basic.

You should be able to determine whether a structure, possibly a cyclohexane, is chiral or achiral by looking at its symmetry or its stereocenters. You should also be able to determine whether a compound, possibly a cyclohexane, is chiral or achiral overall (depending on whether it has at least one achiral conformation).

You should be able to determine whether two structures, possibly cyclohexanes, are:

• skeletal isomers;
• configurational diastereomers;
• configurational enantiomers;
• conformational diastereomers;
• conformational enantiomers; or,
• identical (homomers).

You should be able to identify the sp³ stereocenters in a compound and determine whether they have the R or S configuration.

You should be able to use the mathematical relationship between the ee of a compound, its observed optical rotation, and its specific rotation to calculate any one of these values, based on the other two. You should be able to interconvert the ee and the enantiomeric ratio of a compound.

You should understand the following concepts and be able to use them logically:

• In a chemical reaction, optically inactive starting materials (achiral, or chiral and racemic) give optically inactive products.
• Two enantiomers have the same physical properties (except for optical activity), whereas two diastereomers have different physical properties.
• Although two enantiomers have identical interactions with achiral substances, their interactions with chiral substances, such as living organisms, can differ.
• Two enantiomers can be separated by the process of resolution, which involves a reaction with a chiral, enantiopure reagent.

Given its name, you should be able to draw a substituted cyclohexane in either chair conformation, and you should be able to determine which conformer is higher in energy. Given a table of energies of 1,3-diaxial interactions, you should be able to determine the difference in energy between two chairs, and you should be able to set up the equation that converts this energy into a ratio.

Given a formula, you should be able to tell how many rings and π bonds that compound has, and you should be able to draw several structures with that formula.

You may find these handouts helpful.

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