Chem 1C Exam 2 UCSB

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158 Terms

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molality (m)

moles of solute/mass of solvent (kg)

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volatile

highly unstable; explosive
has some vapor pressure; does evaporate to some extent
can evaporate and will contribute to the vapor pressure of a solution

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nonvolatile

low vapor pressure at room temperature
ex: NaCl, KNO3, C6H12O6

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adding a nonvolatile solute to a solvent

lowers the solvent's vapor pressure

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Raolt's Law for a volatile solvent and a nonvolatile solute

Psolution = Xsolvent * Ppuresolvent

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lower vapor pressure

higher boiling point, higher IMF

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boiling point elevation

Adding a nonvolatile solute to a solvent lowers the vapor pressure of the solution, raising the boiling point of the resulting solution above that of the pure solvent

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freezing point depression

Adding a nonvolatile solute to a solvent lowers the freezing point of the resulting solution below that of the pure solvent (need to remove more energy for the solution to freeze because nonvolatile solute prevents crystallization)

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osmotic pressure

additional pressure needed to prevent or reverse osmosis

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osmosis

diffusion of water across a selectively permeable membrane

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IMF solution > IMF uncombined

strong solute-solvent interaction
process is exothermic (release energy/heat as a result form of bond formation)
Delta H for combination is a large negative, the overall change in enthalpy is negative (exothermic)

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form IMF

release energy

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break IMF

add energy

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delta H (change in enthalpy) for expansion

positive (add energy)

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Enthalpy

total energy of a system

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delta H for combination

negative (release energy)

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IMF solution < IMF uncombined

weak solute-solvent interaction
process is endothermic
Delta H for combination is a small negative, the overall change in enthalpy is positive (endothermic)

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Delta H positive

endothermic

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Delta H negative

exothermic

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like dissolves like

polar dissolves polar
nonpolar dissolves nonpolar
ionic compounds ONLY dissolve in polar solutes

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Entropy

A measure of disorder or randomness.

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positive delta G

non-spontaneous

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negative delta G

spontaneous

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delta G

delta H - T delta S
T (in K) = always positive

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positive delta S

like and like
more disordered

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negative delta S

unlike and unlike
less disordered
ex: water and oil- water will arrange itself around the oil to avoid it

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solubility of solids ____ as temperature increases

increases

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solubility of gases ____ as temperature increases

decreases

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Raolt's Law for a volatile solvent and a volatile solute

Pa = Xa Ppurea
Pb = Xb Ppureb
Psolution = Pa + Pb
Psolution= total vapor pressure of solution
assumes IDEAL solution (where IMFs do not play a factor)

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Negative deviation from Raoult's law

IMF solution > IMF pure substances
lower vapor pressure than expected (ideal solution)
exothermic
solution feels warm

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hydrogen bond donor

hydrogen directly bonded to a N, O, or F atom

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hydrogen bond acceptor

any N, O, or F atom with lone pairs

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Positive deviation from Raoult's law

IMF solution < IMF pure substances
high vapor pressure than is expected (ideal solution)
endothermic
solution feels cold

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non-polar

hydrocarbons, or large hydrocarbons (4+ Cs) w/one O or N

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for elements with 4 or 9 d-orbital electrons

move an electron from s orbital into d orbital

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when forming metal cations

remove s orbital electrons first

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complex ion

charged species consisting of transition metal ion surrounded by ligands

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ligands

molecules or ions that bond to the transition metal ion in a complex ion

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counter ions

Ions that balance charge. Not part of the complex ion.

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ligands attach by

donating a lone pair to form a covalent bond with transition metal

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lewis base

electron pair donor

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lewis acid

electron pair acceptor

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ligand attachment site

any atom with a lone pair
multiple attachment sites are possible only if there are 2+ atoms in between the atoms with lone pairs

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coordination number

the number of bonds to the transition metal

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CN = 2

linear

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CN = 4

tetrahedral

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CN = 6

octahedral

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Splitting of d-orbitals for octahedral complexes

3 on the bottom, 2 on the top
bottom: xz, xy, yz
top: x^2 - y^2 , z^2

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Splitting of d-orbitals for tetrahedral complexes

3 on the top, 2 on the bottom
bottom: x^2 - y^2 , z^2
top: xz, xy, yz
ALWAYS have weak field (high spin case)

<p>3 on the top, 2 on the bottom<br>bottom: x^2 - y^2 , z^2 <br>top: xz, xy, yz<br>ALWAYS have weak field (high spin case)</p>
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weak field ligands

small delta E
Ligands that cause a small difference in the energies of d subshells
can populate top and bottom energy levels at the ground state (can add e- to the top before the bottom is completely full)

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strong field ligands

large delta E
ligands that cause a large difference in the energies of the d subshells
can NOT populate the top and bottom energy levels at the ground state (can only add e- to the top once the bottom is completely full)

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delta E (energy of absorbed photon)

hc/lamda (wavelength)

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wavelength (lamda)

hc/delta E

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you observe the _____ color of light absorbed by the complex

complementary

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shorter wavelength

higher energy

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diamagnetic

all electrons are paired (repelled by magnetic field)

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paramagnetic

unpaired electrons (attracted to magnetic field)

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H2O ligand name

aqua

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NH3 ligand name

ammine

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CO ligand name

carbonyl

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NO ligand name

nitrosyl

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anion ligands

drop suffix (-ide) and add -o

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CO3 2- ligand name

carbonato

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1

no prefix

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2

di

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3

tri

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4

tetra

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5

penta

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6

hexa

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Use greek prefixes when naming

ligands that already contain a prefix (ex: en)
write greek prefix then ligand name in parenthesis

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1 (greek)

none

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2 (greek)

bis-

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3 (greek)

tris-

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4 (greek)

tetrakis-

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when complex ion is an anion

add -ate to the end of the metal name

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Fe (in anionic complex)

ferrate

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Cu (in anionic complex)

cuprate

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Pb (in anionic complex)

plumbate

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Ag (in anionic complex)

argentate

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Au (in anionic complex)

aurate

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Sn (in anionic complex)

stannate

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Mo (in anionic complex)

molybdate

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Isomer

Compounds with the same formula but different structures.

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structural isomers

differ in the covalent arrangements of their atoms (different types of bonds)
ligands swap places in coordination compound
coordination isomers and linkage isomers

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Stereoisomers

Compounds with the same structural formula but with a different arrangement of the atoms in space (same bonds, different spatial arrangements)
geometric and optical

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linkage isomers

ligand is bound to the metal by a different atom (different binding site on the ligand)

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cis (geometric isomer)

same ligands are side by side

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trans (geometric isomer)

same ligands are across from each other

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MX4X2

octahedral complex capable of forming cis/trans isomers

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MX2X2

square planar/tetrahedral complex capable of forming cis/trans isomers

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linkage isomers are possible when

there are two distinct attachment sites on ligands

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geometric isomers are possible when

MX4Y2
MX2Y2

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organic molecules

molecules that contain carbon

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alkanes

CnH2n+2
saturated hydrocarbons, single bonds
always non-polar
low boiling points
low reactivity
suffix -ane

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1 carbon

meth

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2 carbons

eth

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3 carbons

prop

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4 carbons

but

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5 carbons

pent

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6 carbon

hex