Chem Final Flashcards
alpha particle
4, 2 He
condensation polymerization
creates polymer + water
- monomer will be ester or amide
beta particle
0, -1 e
positron particle
0,1 e
gamma particle
0,0 γ
neutron particle
1,0 n
radiation emission
particle is a product
radiation capture
particle is a reactant
nucleon
p + #n
hydrogenation organic rxn
yields saturated alkane (single bonds, additional 2 hydrogens)
combustion organic rxn
add O2 to produce CO2 and H2O
condensation organic rxn
forms small molecule
esterfication
alcohol + carboxylic acid -> ester + H2O
amine + carboxylic acid
-> amide
homopolymer
same monomer
copolymer
diff. monomer
addition polymerization
break multiple bond to form multiple single bonds
What gets the lowest #C priority in naming ?
functional groups
Alcohol functional group
-OH
-suffix ‘ol’
-prefix ending of multiple alcohols
ex) ethanediol
ether functional group
-O
-name longest chain
- #C for branch w/ suffix ‘oxy’
aldehyde functional group
H-C=O
- suffix ‘al’
relationship between IMF and volatility
higher IMF, lower volatility
relationship between Pvap and temp
higher pvap, higher temp
relationship between molality and bp/fp
higher molality, lower fp, higher bp
sublimation
solid to gas
straight line of heating curve formula
q=m ΔH
sloped line of heating curve formula
q=mC ΔT
1st order K units
s^-1
2nd order K units
1/Ms
0 order K units
M/s
intermediate
1st a product, then a reactant
-not in rate law
catalyst (in rate law)
1st a reactant, then a product
- not in rate law
relationship between #e- and IMF strength
higher #e-, higher IMF strength
hydrogen bonding atoms
H bonded to NOF
IMFs responsible for
-surface tension
-capillary action
-viscosity
catalyst
-speed up rxn by lowering activation E
rxn mechanisms
series of elementary steps
qualifications for a good rxn mechanism
- sum gives overall rxn
- rate law agrees w mechanism
collision theory
rate of rxn is proportional to # of effective collisions
effective collisions
- have enough EA
- proper orientation
activation E of reverse rxn (exo)
ΔH+Ea (forward)
Ea of reverse rxn (endo)
Ea (forward) - ΔH
factors affecting rate
- properties of R and P
- ability of Reactants to come into contact
- Conc (higher)
- Temp (higher)
- catalysts
Length of half lives
1st order: constant
2nd order: longer
0 order: shorter
inverse trend for rate
0 order straight line plot
[A] vs. t
rate
change in [ ] over time
slope tells us
instantaneous rate
integrated rate law
rate over time
kinetics
focus on rxn rates
1st order straight line
ln[A] vs t
2nd order straight line
1/[A] vs t
Face centered cubic
-4 total atoms
-edge=r√8
close packing
=FCC cell
ionic solid unit cell
must reflect stoichiometry
small ΔE conductivity
good conductor
large ΔE conductivity
good insulator, poor conductor
intermediate ΔE conductivity
semiconductor
vapor pressure
pressure of gas above solid or liquid
volatile
easily vaporizing
relationship between T and VP
higher T, higher VP
relationship between VP and BP
higher VP, lower BP
simple cubic
1 atom
body centered cubic
2 atoms
(endo) relationship between T and Ea
higher T, lower Ea
(exo) relationship between T and Ea
no effect
branches effect on surface area and BP
more branches , lower SA, lower BP
crystalline solid
ordered repeating lattice
UNIT CELL`
smallest repeating unit
octahedral crystal field theory
-bonding on axis
-Δ depends on ligand strength
tetrahedral crystal field theory
-bonding between axis
-Δ small
- e- promotion
square planar crystal field theory
-bonding on x & y axis
-Δ large
-e- pairing
weak field ligand
Δ is small, e-promotion
strong field ligand
Δ is large, e- pairing
(Raoult’s Law) No interactions
-ideal soln
-np/np
-expected vp
(Raoult’s Law) Unfavorable interactions
-p/np
-positive deviation (+ ΔH)
-VP higher
(Raoult’s Law) Favorable interactions
-p/p, diff IMF
-negative deviation (-ΔH)
-VP lower
isotonic
same osmotic pressure
relationship between pressure and concentration
higher pressure, higher conc
structural isomer
diff formula and name
stereoisomer
same bonds, diff orientation and names
optical isomers
mirror image, not superimposible
can tetrahedral have geometric isomers?
NO
eg
-on axis
-x^2-y^2, z^2
t2g
-between axis
-xy, yz, xz
ligand
lone pair, e- donor
how are ligands bonded to TM?
covalent bonds
monodentate
ligand has 1 binding site
polydentate
ligand has 1+ binding sites
When are complexes white/transparent
when all e-‘s are paired
alkanes
single bonds only
alkenes
double bond
alkyne
triple bond
asymmetric center / optical isomer when
when atom is bonded to 4 diff groups
what position should the double bond be in a cyclic carbon
1&2 position
aromatic compounds
alternating double bonds
ketones
=O
suffix ‘one’
carboxylic acid
O=C-OH
suffix ‘oic acid’
esters
O-C=O
branch on single bonded O ends in ‘yl’
branch on double bonded O ends in ‘oate’
amines
-N
name with suffix amine
#C where branch is attached to N
short chain suffix ‘yl’