University12 min

Stereochemistry: assigning R/S and Z/E

Rank substituents with the CIP rules, duplicated multiple bonds included, then read R or S and Z or E without getting the direction wrong.

The essentials

1

Stereoisomers and the asymmetric carbon

Stereoisomers share the same connectivity but differ in spatial arrangement. An asymmetric carbon C\text{C}^* bears four different substituents. Two enantiomers are non-superimposable mirror images; stereoisomers that are not mirror images are diastereomers. With nn asymmetric carbons: at most 2n2^n stereoisomers.
2

CIP rules: the ranking

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3

Multiple bonds: duplication

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4

Reading R or S

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5

Reading Z or E

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