Organic final – Flashcards
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Aufbau |
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The lowest energy orbital is filled first |
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Pauli exclusion principal |
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Each orbital can accommodate a max of 2 electrons that have opposite spins |
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Hund's rule |
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Dealing with degenerate orbitals such as p orbitals one election is placed in each degenerate orbital first, before electrons are paired up |
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Sigma bond |
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Overlap of 1s orbital. All sigma bonds are sigma bonds |
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VSEPR |
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VAlence shell electron pair repulsion theory. Electrons are as far away from each other as possible. |
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Steric number |
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In order to predict the geometry of a small compound, small compound, we focus on the central atom and count the number of sigma bonds AND lone pairs. The total is the steric number. |
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If steric number is 4 |
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Must use 4 orbitals - sp3 hybridized. Tetrahedral. (if no lone pairs=tetrahedral) if one lone pair= trigonometry pyramidal. (two lone pairs--bent) |
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Steric number 3 |
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Sp2 hybridized ( double bonds) if one lone pair it's bent, if none then it's trigonal planar |
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Steric number 2 |
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Sp hybridized. linear. |
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Double bonds are |
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Sp2. has 2 bonding interactions, 1 sigma and 1 pi bond. |
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Triple bonds are |
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Sp. Has three bonding interactions, one sigma and two pi bonds. |
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Each molecuele on the end of a sigma bonds |
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Own 1 of the electrons |
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Difference in electronegativity values less than .5 |
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Covalent bond |
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Difference in electronegativity values between .5 and 1.7 |
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Polar covalent |
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Difference in electronegativity values greater than 1.7 |
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Ionic bond |
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Dipole dipole interactions |
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Electronegativity difference between atoms in a molecule. Attraction between molecules results in an elevated melting and boiling point |
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Hydrogen bonding |
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Protic compounds- proton connected to an electronegative atom. More hydrogen bonds- higher boiling point |
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Fleeting dipole dipole interactions |
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Hydrocarbons- boiling point increases with molecular weight |
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Brancing of hydrocarbons |
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Cause decrease in boiling point. |
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Carbocations |
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Sp2 |
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Bronsed lowery acid/ base |
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Proton donor/ proton acceptor |
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High pka |
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Weak acid |
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Vinylic |
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The atoms bearing double bonds |
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Allylic |
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Adjacent to double bonds |
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Eclipsed conformation |
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Highest in energy |
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Staggered |
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Lowest energy conformation |
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Anti conformation |
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Less steric hendrance |
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Gauche |
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Overlap |
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Diastereomers |
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Sterioisomers that are not mirror images of one another (ex cis and trans) |
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Meso compounds |
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2 chiral centers on adjacent Cs, ALWAYS RS |