Umaine Organic Chemistry Exam 2 – Flashcards

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alkane
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hydrocarbons that lack pi bonds
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how to name alkanes
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1. identify parent compund 2. name substituents 3. number the carbon atoms and assign a locant to each substituent 4. assemble substituents alphabetically.
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propyl
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3 carbon atoms
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butyl
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4 carbon atoms
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pentyl
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5 carbon atoms
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naming bicyclic compounds
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1. identify bicyclo parent, indicate bridgeheads 2. identify and name substituents 3. # parent chain (start with longest bridge) and assign locant to each subsitituent 4. assemble substituents alphabetically
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staggered newman projection
staggered newman projection
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-more stable (favored) -lower energy
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eclipsed newman projection
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-less stable -higher energy
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anti conformation
anti conformation
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-more stable -lower energy
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gauche conformation
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-less stable
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chair conformation stability
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equitorial position is favored, has lower energy
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cis-trans stereoisomerism
cis-trans stereoisomerism
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cis- same side of ring trans- opposite sides of ring
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stereoisomer
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same formula and constitution, different spatial arrangement of atoms
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superimposable
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mirror image is identical to the object (achiral)
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chiral
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objects that are not superimposable
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chirality center
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tetrahedral carbon bearing 4 different groups
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enantiomers
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when a compound with one chirality center has one superimposable mirror image
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assigning configuration (R&S)
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1. identify 4 atoms attached to chirality center and prioritize by atomic # 2. rotate molecule so that the 4th priority is on a dash 3. identify direction of 1-2-3 sequence, clockwise=R, counterclockwise=S
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optically pure
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a solution containing a single enantiomer
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racemic mixture
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-a solution with equal amounts of both enantiomers -optically inactive
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diastereomers
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stereoisomers that are not mirror images
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max # of stereoisomers
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2^n where n= # of chirality centers
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rotational symmetry
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-has an axis of symmetry -rotates 180 degrees -chirality is not dependent on it
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reflectional symmetry
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-has a plane of symmetry -a compound that possesses a plane of symmetry is achiral
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meso compound
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contains chirality centers but is achiral because it possesses reflectional symmetry
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fischer projections
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-vertical lines are dashes (go behind the page) -horizontal lines are wedges (come out of the page)
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