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54 Cards in this Set

  • Front
  • Back
define acid
substance that behaves as a proton (H+) donor

proton donor
define base
substance that behaves as a proton (H+) acceptor

proton acceptor
define conjugate acid
formed when the base accepts a proton
define conjugate base
formed when the acid donates a proton
define conjugate acid-base pair
the acid and base on the opposite sides of the equation
dissocation of acid-base
production of positive and negative ions when an ionic compound dissolves in water
ion product for water
kw = ....
1.0 x 10-14
polyprotic substances
substance that can accept or donate more than one proton per molecule

monoprotic
diprotic
triprotic acids
strong acids/bases
reaction with water is virtually 100% (strong electrolytes)
examples of strong acids
HCl
HBr
HI
HNo3
H2So4
HClO4
examples of strong bases
NaOH
KOH
Ba(OH)2
all metal hydroxides
examples of weak acids/bases
(only a small % dissociates- weak electrolytes)
acid- acetic acid CH3COOH
carbonic acid H2Co3

base- ammonia NH3
pyridine C5H5NH2
strong vs weak
acid/base
strong - lots of hydronium ion or hydroxide ion; good electricity (electrolytes); virtually no starting compound left

weak - relatively little hydroxide/hydronium ion; poor conductors of electricity; only a tiny fraction of molecules react
ionization
dissocation of acids and bases
neutralization reaction
reaction of an acid with a base to produce a SALT and a WATER

HCl (aq) + NaOH (aq) --> NaCl (aq) + H20 (l)

acid/base-->salt/water
spectator ions
ions appearing the same on both sides of the equation
describe a titration
1. addition of measured amounts of known conc. to a buret to neutralize the second unknonwn sol'n
equivalence pt is signaled by the indicator
equivalence point
moles of added acid and base are equal

MaVa = MbVb
buffer solution
solution which resists large changes in pH when either acids or bases are added

consist of either
1. weak acid and its salt
2. weak base and its salt
buffer capacity
measure of the ability of a solution to resist large changes in pH when a strong acid/base is added
buffer range
value of pH over which a solution to resist large changes in pH when a strong acid or base is added
organic
has covalent bonds
molecules, nonelectrolytes
inorganic
usually ionic bonds
3D crystal structures, often H2O soluble, dissocating into ions (electrolytes)
aliphatic hydrocarbons
break into
1. alkanes
2. cycloalkanes
3. alkenes
4. alkynes
aromic hydrocarbons
contain a benzene ring or derivitate a benzene ring
functional group
an atom or group of atoms arranged in a particular way
-primarily responsible for the chemical/physical properties of the molecule in which its formed
saturated hydrocarbons
contain only a carbon-carbon single bond

alkane
unsaturated hydrocarbon
contain a double or a triple bond

alkene/alkyne
constitutional isomers
two molecules having the same molecular formulas, but different chemical structures
structural isomers
molecules having the same molecular formula, but different chemical structures
symmetrical
same atom or functional group is added to each carbon
hydrogenation, h2
halogenation Br2, Cl2
unsymmetrical
hydrogen and another atom are added to the functional group
hydrohalogenation, HCl, HBr
hydration, H2O (requires a strong catalyst)
hydrogenation
addition of a molecule of H2 to a carbon-carbon double bond to produce an alkane
uses Ni, Pt, Pd as a catalyst
halogenation
addition of a molecule of halogen (X2) to a carbon-carbon double bond
does not require a catalyst
hydration
addition of H2O
requires a catalyst, H+
presence of a strong acid
markovnikov's rule
when an acid adds to a double bond, H of the acid often goes to the end of the double bond which had more hydrogens attatched initially

"the rich get richer"
alkene formula
CnH2n
planar (shape) of alkenes
all atoms lie in a single plane

C-C=C-C
alkyne formula
CnH2n-2
linear (shape) of alkynes
2 carbon atoms are bonded by a triple bond, each bond angle is at 180degrees
linear
straight line
geometric isomers
occur when there are two different groups on each of the carbon atoms attached by the double bond
cis isomer
two similar groups are on the same side of the double bond
trans isomer
two similar groups are on the opposite sides of the double bond
polymer
macromolecules composed of repeating structural units called monomers
addition polymers
~~[R-R-C-C-R-R-]~~
eth-
2
prop-
3
but-
4
pent-
5
hex-
6
hept-
7
oct-
8
non-
9
dec-
10