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deals with the changes in energy that take place when processes such as chemical reactions occur; extent at which a reaction goes to completion |
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concerns the velocity or rate at which the concentrations of reactants & products change; speed at which a reaction goes to completion |
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a transformation that yields the most stable products |
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a reaction in which the product obtained is the one formed fastest |
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when the concentrations of reactants & products no longer change |
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when a reaction goes to completion; indicated by a large value for K |
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equation for K (equilibrium constant) |
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[products][products] _____________________
[reactants][reactants] |
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equation for Gibbs standard free energy change (delta G degrees) related to K |
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equation for Gibbs standard free energy change related to enthalpy & enropy |
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the heat absorbed or released at constant pressure during the course of the reaction |
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equation for enthalpy change in a reaction |
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(sum of bonds broken) - (sum of bonds formed) |
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when the bonds formed are stronger than those broken; negative H; releasing heat |
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positive H; heat-absorbing |
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plots energy as a function of reaction progress |
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the combined processes of bond breaking & bond formation that constitutes the overall change from the structures of the starting compounds into those of the products; how reaction progress is measured |
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when the energy of a reaction first rises to the maximum |
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the energy input required to raise the energy of the starting compounds to that of the transition state |
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Boltzmann distribution curve |
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depicts the distribution of kinetic energy |
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proportionality constant "k" in rate equation |
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a reaction for which the rate depends on the concentrations of two molecules |
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the rate of the reaction only depends on the concentration of one reactant |
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a basic atom when it attacks an atom other than hydrogen |
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acid dissociation constant (Ka) |
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Ka=K[H2O] = ([H3O+][A-])/[HA] * molL^-1 |
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the species A- derived from the acid HA |
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the species HA derived from the base A- |
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a species that contains an atom that is at least two electrons short of a closed outer shell |
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contains at least one lone pair of electrons |
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organic compounds possessing carbon-halogen bonds |
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center of chemical reactivity |
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functional groups/functionalities |
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the atoms or groups of atoms that tend to be the site of high chemical reactivity on molecules |
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hydrocarbons which contain only single bonds |
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molecules whose carbons form a ring |
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hydrocarbons with double bonds |
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hydrocarbons with triple bonds |
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contain polar carbon-halogen bonds as their functional groups |
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contain an oxygen bonded to two carbon atoms; -C-O-C- |
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carbonyl functional group |
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contains the carbonyl group and an -OH |
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replacement of oxygen in alcohols by sulfur |
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the carbon chain contains one or several branching points |
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one attached directly to only one other carbon atom |
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a carbon attached directly to two other carbon atoms |
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a carbon attached directly to three other carbon atoms |
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a carbon attached directly to four other carbon atoms |
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the longest carbon chain in a molecule |
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groups other than hydrogen that are attached to a carbon chain |
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the energy required to move the hydrogen atoms past each other |
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there is _____ about all single bonds at room temperature |
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the many forms of a molecule that are created by rotations of the functional groups |
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the study of conformations' thermodynamic & kinetic behavior |
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rotational energy/torsional energy/torsional strain |
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the change in energy resulting from bond rotation from the staggered to the eclipsed conformation |
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the lowest energy state of a molecule |
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the difference in energy between ground and transition states |
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the most stable arrangement of a molecule; steric hindrance is minimized (functional groups are as far from each other as possible) |
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general structure: haloalkanes |
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general structure: alcohols |
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general structure: ethers |
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general structure: thiols |
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general structure: alkenes |
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general structure: alkynes |
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general structure: aromatic compounds |
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ring of carbons (alternating double bonds) |
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general structure: aldehydes |
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general structure: ketones |
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general structure: carboxylic acids |
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general structure: anhydrides |
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general structure: esters |
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general structure: amides |
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general structure: nitriles |
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general structure: amines |
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pKa: CH3-aromatic-S(double bonded to two oxygens)-OH |
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pKa: R - C - C - H ll l O H2 |
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