4Types of Isomers. 1. Structural Isomers/(Constitutional) 2. Geometric Isomers/(Cis/Trans) 3. Optical Isomers A. Enantiomers B.

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4Types of Isomers 1. Structural Isomers/(Constitutional) 2. Geometric Isomers/(Cis/Trans) 3. Optical Isomers A. Enantiomers B. Diastereomers

4Types of Isomers C 4 10 C 4 10 O O O O O O O O O O O O C 3 C 3 C 3 C 3

Structural Isomers Same Different Chemical Formula Structure Chemical Properties Physical Properties Biological Properties Example C 4 10 C 4 10

Geometric Isomers Chemical Formula Structure Same Example Different Geometry (around C=C) Chemical Properties Physical Properties Biological Properties C 4 6 2 Cis-2,2-dichloro-2-butene C 4 6 2 Trans-2,2-dichloro-2-butene

Optical Isomers (Enantiomers) Definition: Chiral molecules that are mirror images of each other. Same Chemical Formula Structure Chemical Properties Physical Properties Different Geometry stereoisomers that are mirror images Optical Rotation Biological Properties

Optical Isomers (Diastereomers) Definition: Chiral molecules that are not enantiomers of each other. Differ in the orientation around one chiral carbon. Same Chemical Formula Structure O O Different Geometry stereoisomers that are not enantiomers Chemical Properties Physical Properties Optical Rotation Biological Properties O O O O C 3 C 3

Enantiomers vs. Diastereomers O Enantiomers O O O O O Diastereomers O C 3 O C 3 Diastereomers O O O O C 3 C 3 Enantiomers

Plane Polarized Light Light normally oscillates/vibrates in every direction: Plane Polarized Light oscillates/vibrates in only one direction: Plane Polarized Light can interact with molecules:

Optical Rotation of Plane Polarized Light Enantiomer A Enantiomer B

Chiral Molecules Definition: Molecules that lack a plane of symmetry, and therefore have non-superimposable mirror images. Can rotate plane polarized light. Requirements: Carbon atoms with 4 bonds to different groups. No additional plane of symmetry. Important: Chiral molecules that are enantiomers have the same physical and chemical properties but different biological properties.

Achiral Molecules Molecules that possess chiral carbons but have an additional plane of symmetry They do not rotate plane polarized light. Meso compounds are achiral. C 3 C 3 No Plane of Symmetry C 3 Achiral/Meso C 3 Chiral

Fischer Projections Method for drawing chiral molecules in 2D. Always draw the most oxidized group at the top The carbon backbone is drawn top-bottom Swaps are allowed only for horizontal atoms Odd number of swaps = diff. molecule Even number of swaps = same molecule O C 3 O O 3D View showing tetrahedral shape 2D Representation of a 3D shape

Dextrorotatory and Levorotatory Dextrorotatory Rotates light clockwise (+) Levorotatory Rotates light counter clockwise (-)

MesoCompounds Definition: Mesocompounds have 2 (or more) chiral atoms, but do not rotate plane polarized light due to have an extra plane of symmetry Extra plane of symmetry Mirror image = same molecule Does not rotate plane polarized light Mirror same molecule

Number of Stereoisomer Maximum number of stereoisomers 2 n n = number of chiral carbons 2 2 = 4 2 3 = 8 2 4 = 16 Mesocompounds decrease the number of isomers formed

Racemic Mixtures Definition: A mixture of equal amounts of two enantiomers Does not rotate plane polarized light (the 2 enantiomers cancel each other out)

Same/Different Two Fischer projections: Even # swaps = same molecule Odd # swaps = different molecule Different O Br C 3 O O Br C 3 C 3 Br Same Same

Identifying Chiral Carbons Definition: Chiral carbons are bonded to 4 different groups of atoms no C=C or C C watch out for same groups like methyl/ethyl chiral 4 different groups methyl ethyl propyl

Enantiomers Definition: Chiral molecules that are non-superimposable mirror images of each other. Same chemical and physical properties Different optical activity and biological properties Mirror

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