ch 19 Flashcards

1
Q

deviations from raoult’s law
list the /possible interactions

A

no interactions
unfavorable interactins(repulsion)
favorable interactions

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2
Q

deviations from raoult’s law
no interactions =

A

ideal solution; two nonpolars
VP is as expected
delta H = 0

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3
Q

deviations from raoult’s law
unfavorable interactions

A

repulsions
one pushes other out of the solution –> gas
polar+ nonpolar
VP is higher than expected, positive deviation
delta H = positive –> endothermic

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4
Q

deviations from raoult’s law
favorable interactions

A

solution interactions are stronger than components
more interactions as a solution
“keep” components in solution
VP lower than expected
delta H negative –> exothermic

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5
Q

complex ion

A

transition metals surrounded by ligands
covalent bond between transition metals and ligands
transition metal is e- acceptor
ligands are e- donors

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6
Q

[Co(NH3)6] (NO3)3
label the components

A

[Co(NH3)6]NO3)3 = coordination compound
[Co(NH3)6] = complex ion
Co = transition metal
NH3 = ligand
NO3 = counter ion
counter ion and complex ion connected by ionic bond –> break in solution

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7
Q

coordination number

A

bonds to central transition metal

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8
Q

types of ligands

A

ligands must have a lone pair

neutral = NH3 and H2O
charged= Cl-
monodentate
polydentate

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9
Q

coordination number and relative shape

A

2= linear
4= tetrahedral or square planar
6 = octahedral

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10
Q

monodentate vs polydentate

A

monodentate = one binding site for ligand ( one transition metal to bind to)
polydentate = more than 1 bonding site
- polydentate must have multiple lone pairs and at least 3 to 4 atoms between lone pair bonding sites of ligands

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11
Q

ethylenediamine (en)

A

H2NCH2CH2NH2
C2H6N2

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12
Q

naming coordination compounds

A
  1. cation first
  2. ligands before metal
  3. if complex ion is anion, add “ate” to metal
  4. oxidation state is written in roman numerals
  5. alphabetical order of ligands
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13
Q

naming ligands in coordination compounds;
H2O
NH3
CO

A

H2O = aqua
NH3 = ammine
CO - carbonyl

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14
Q

naming ligands in coordination compounds;
anion
Cl =
OH=
CN=

A

Cl = chloro
OH - hydroxo
CN = cyano
end in “o”

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15
Q

naming ligands in coordination compounds;
ide =
ate =
ite =

A

ide = o
ate = ato
ite = ito

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16
Q

prefixes for # ligands
2,3,4…

A

2 = di
3 = tri
4 = tetra

17
Q

prefixes for polydentate ligands 2,3,4

A

2 - bis
3 - tris
4 - tetra

18
Q

name the folllowing
K4[Ni(CN)4]
K2[Cr(H2O)2(C2O4)2]
[Fe(H2O)5OH]Cl2

A

potassium tetracyanonickelate(0)
potassium diaquabisoxylatochromate(II)
pentaaquahydroxoiron(III) chloride

19
Q

what is the formula
tris(en)cobalt(III) sulfate

A

[Co(en)3]2(SO4)3

20
Q

isomers

A

compounds with the same number and type of atom but are structurally different
structural and stereoisomers

21
Q

structural isomers

A

different bonds
different formula
different name
[MASB]C
[MASC]B

difference in linkage

22
Q

stereoisomers

A

same bonds, different orientation
same formula
different name

23
Q

geometric stereoisomers

A

cis and trans isomers
cis = AA
BB
trans = AB
BA

24
Q

optical stereoisomers

A

one molecule is mirror image
cannot superimpose

25
Q

which one of the following complexes can have geometric isomers?
A. [Pt(NH3)2Cl2] = square planar
B. [Zn(NH3)2Cl2] = tetrahedral
C. [Cu(NH3)4]2+ = square planar
D. [Cu(NH3)5Cl]2+ = octahedral
E. All

A

A. [Pt(NH3)2Cl2] = square planar

tetrahedrals can’t have geometric isomers since their geomtry isn’t flat (not on same plane)

square planar C has 4 of the same ligands –> can’t make cis/trans

octahedral has 5 same ligands and 1 Cl –> ca’t make cis/trans

26
Q

crystal field theory

A

consider d-orbital orientations and covalent bonds to transition metals

eg = e- density on axis –> dx^2-y^2 and dz^2
t2g = e- density between axes –> dxy dxz dyz

caused by e-/e- repulsions between e- in d-orbitals and e- in covalent bonds

27
Q

d- orbital diagram for octahedrals

A

6 covalent bonds
90 degrees
ligaments bond ON axis
^
| _____ _____ eg
| _______ ______ _____t2g

28
Q

d-orbital diagram for tetrahedral

A

4 covalent bonds
109.5 degrees
ligands bond between axis

  • __ ____ ____ t2g
  • ___ ____ eg

______ _____ ______ t2g

29
Q

d-orbital diagram for square planars

A

bonds lie on axis
* _____ dx^2-y^2
* ___ dxy
* ___dz^2
* ___ dxz ___ dyz

___ dx^2 - y^2

30
Q

look over the shapes of each of the d-orbital levels

A
31
Q

splitting energy

A

2 competing effects
1. energy costs from pairing
2. energy costs from promotion

when the splitting energy is small… electrons would rather be promoted(unpaired electrons) (high spin)

when the splitting energy is large – electrons would rather be paired (low spin)

32
Q

list the general splitting energies for
tetrahedral
square planar
octahedral

A

tetrahedral = small splitting energy
square planar = large splitting energy
octahedral = look at spectrochemical series

33
Q

large splitting energy =

A

paired electrons

34
Q

small splitting energy

A

unpaired electrons
rather be promoted

35
Q

color emission of compounds

A

result of e- transition between eg and t2g
electrons can absorb photon for promotion
we see reflected light (opposite of color wheel)

36
Q

calculate energy and wavelength using what equation

A

E=hc/wavelength
h = 6.626x10^-34 J*s
E = Joules per photon