Chapter 2 - Isomers
Quiz yourself by thinking what should be in
each of the black spaces below before clicking
on it to display the answer.
Help!
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isomers | chemical compounds that have the same molecular formula but differ in structure
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structural isomers | compounds that share only their molecular formula
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stereoisomers | same formula and the same atomic connectivity
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geometric isomers | differ in whether it is cis or trans
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Z | cis/same side
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E | trans/opposite side
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chirality | object that is not superimposable upon its mirror image
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achiral | mirror images that can be superimposed; like the letter A
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enantiomers | chiral mirror images; optically active
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R | clockwise order of substituents, right turn with steering wheel
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S | counterclockwise order of substituents, left turn with steering wheel
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Fischer Projections | 2D representation of 3D molecule; horizontal lines come out of the page; Hydrogen should be vertical
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Meso Compounds | not optically active, plane of symmetry
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+/D | rotates polarized light to the right
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-/L | rotates polarized light to the left
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diastereomers | stereoisomers that are not mirror images
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conformational isomers | differ by rotation about one or more single bonds
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Newman Projection | representation of different configurations
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most stable configuration | anti staggered
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Gauche | 60 degrees apart
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Eclipsed | 120 degrees apart
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Totally eclipsed | 0 degrees apart, right behind each other
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most stable configuration for cyclohexane | chair, boat is second
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You may also shuffle the rows of the table by clicking on the "Shuffle" button.
Or sort by any of the columns using the down arrow next to any column heading.
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