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 |