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[Cu(H2O)6]2+, from copper sulfate.5H2O (s)
pale blue
vandium 2+ in solution
Violer
Vandium 3+ in solution
Green
VO+
yellow
Cr3+ (2)
Violet when surrounded by 6H2O, but normally substituted to be green
VO2+ (V is charge 4+)
blue
Cr2 O7 2-
Orange
Mn2+
light pink
MnO4 2-
green
MnO4 -
Purple
Fe 2+ in solution
light green
Fe 3+ in solution
yellow
Co 2+ in solution
pink
Ni 2+ in solution
green
Cu 2+ in solution
blue
Ti 2+ in solution
violet
Ti 3+ in solution
purple
When OH- or NH3 - is added to aqueous solution of Cu2+
pale blue precipitate of cu(OH)2(H2O)4 (s)
When OH- or NH3 - is added to aqueous solution of Fe2+
Fe(OH)2 (s) dark green / dirty green precipitate
When OH- or NH3 - is added to aqueous solution of Fe3+
Fe(OH)3 (s), orange-brown precipitate
When OH- or NH3 - is added to aqueous solution of Mn2+
pale pink / pale brown precipitate of Mn(OH)2
When OH- or NH3 - is added to aqueous solution of Cr3+
dark green precipitate Cr(OH)3
Adding excess of NH3 to Cu2+
dark blue solution, [Cu(NH3)4(H2O2)2] 2+
excess HCL to Cu2+
CuCl4 2-, yellow
Reduction of Cu2+ with I-
white precipitate (CuI) and brown I2
Cu colour
brown solid
CoCl2.6H2O(s) plus water and excess HCl
CoCl4 2–, blue
excess NH3 to Cr 2+(aq)
[Cr(NH3)6] 3+, purple solution
MnO4 – /Fe2+ Mn2+/Fe3+
purple (MnO4 – ) to pale pink (Mn2+) (in titrations, so dilute that it is practically colourless)
transition element definition
d-block element that can form atleast one stable ion with a partially filled (incomplete) d-subshell
why do orbitals fill up singly then double up
electrons repel eachother
Which d-block elements aren’t transition elements
scandium and zinc
max amount of electrons d subshell holds
10
What’s so special about the electron configuration of copper and chromium?
electron from 4s orbital moves into the 3d orbital to create a more stable half full or full 3d subshell respectively
Why aren’t scandium and zinc transition elements
scandium only forms the stable ion Sc3+ which has an empty subshell
zinc only forms he stable ion Zn@+ which has a full d subshell
Why do we always remove 4s orbitals before 3d (2)
electrons are further away from nucleus in 4s
higher energy, less attraction to nucleus
3 properties of transition elements
variable oxidative states
form coloured ions in solution
can be used as catalysts
explain the variable oxidative states of transition elements (3)
electrons sit in 4s and 3d energy levels, which are very close
electrons can transition readily between 4s and 3d orbitals
electrons ae gained and lost using a similar amount of energy when they form ions
first ionisation energies are very small, small amount of energy to remove electrons
explain how transition elements can be good catalysts, and why that’s good (3)
transition metals have variable oxidative states so they are good catalysts by receiving and losing some electrons in the 4s/4d orbitals to speed up reactions
have surfaces that allow substances to adsorb to the surface which lowers Ea of reaction
products are made faster at lower temp, saving energy and money, better for the environment
risks of using t metals as catalysts (2)
long term copper exposure: damage to liver. ring of copper in eye is sign of copper poisoning
long term exposure to manganese causes psychiatric issues and physical tremors
Cu2+ is used as a catalyst for…
reaction of Zn with acids
`MnO2 is used as a catalyst
decomposition of H2O2
Complex meaning
transition metal forms a complex of a central metal surrounded by ligands. held together by coordinate / dative bonds
ligand definition and examples
molecule or ion with lone electron pair that is able to form a dative (coordinate) bond to the central metal ion by donation of this electron pair
Cl-, H2O, NH3
Monodentate ligand definition and examples
form one coordinate bond, eg. H2O, Cl-, NH3
bidentate ligand definition and examples
form two coordinate bonds
eg. NH2CH2CH2NH2
dative / coordinate bond definition
covalent bond where both shared electrons in the bond come from the same atom
Excess OH- to Cr3+
green solution
Coordination number
total number of coordinate bonds formed with the central metal ion
why are transition metals identifiable by their colour (4)
colour depends on coordination number, type of ligand bonded, and oxidation state
colour arises because of how substances absorb and refect light
ligands cause d orbitals to split, so electrons exist in slightly higher energy level in excitated state
change of energy between these states corresponds to specific wabelength and frequency of light
why can some ions be colourless
no available electrons
so no excitation of electrons so no different energy levels
tetrahederal complex bond angle
109.5
what two transition elements have a square planar shape with a bond angle of 90
platinum and nickel complexes
describe cisplatin (6)
cis isomer of square planar complex of platinum
chlorine atoms are on same side
cancer therapy drug
target components of cells that are chiral
onle one single isomer will work to cure disease
causes serious side effects eg. hair loss so must be used in small amounts
Are Cl- or H2O and NH3 ligands larger
Cl- ligands are larger
Coordination number of Cl- ligands is always
4
Describe the chelate effect (3)
bidentate / multidentate ligand will substitute monodentate ligand
because there will be more particles / mols on right hand side, so entropy is positive (higher disorder between particles)
entropy is positive, free energy is negative, so feasible.
enthalpy change of ligand substitution reactions (2)
very small
bonds being formed are very similar to bonds being broken
With aqueous sodium hydroxide, metal aqua ions react as…
acids
order of tests for anions
carbonate
sulfate
hallide
testing for carbonate(CO3 2-) and hydrogencarbonate (HCO3 - )
when acid such as HCL is added, substance containing carbonate ions will fizz and CO2 gas is given off
collect gas and bubble through limewater which will turn cloudy to confirm identity
test for sulfate ions
uses acidified BaCl2, which reacts to form a white precipitate of barium sulfate
tesing for hallide ions
acidified nitrate with ethanol as solvent: Cl - white precipitate, Br- cream precipitate, I- yellow precipitate
dilute NH3: Cl- precipitate dissolves
onc. NH3: Cl- and Br- precipitate dissolves
test for ammonium (NH4+)
add NaOH and gently warm
forms ammonia gas, which is basic
hold red damp litmus paper over substance. blue = ammonium
[Cu(H2O)6] 2+ colour
Pale blue
Cu(OH)2 (s) colour
Pals blue precipitate
[Cu(NH3)4(H2O)2 ]2+ Colour
Dark blue
CuCl4
2–
Yellow
Cu+
White precipitate (CuI) and brown I2
Cu2+ / Cu colour
Disproportionately of Cu+
Brown solid (Cu) and blue solution ( CuSO4)
CoCl4
2–
from CoCl2.6H2O(s) plus
water and excess HCl
Blue
[Cr(H2O)6]3+
from KCr(SO4)2.12H2O(s)
(heat green)
Due to impurities, it is
common for Cr(III) to
appear green in solution
If precipitate from silver nitrate dissolves in dilute ammonia it’s
Chloride
If precipitate from silver nitrate dissolves in concentrated ammonia it’s
Bromine
If precipitate from silver nitrate does not dissolve in concentrated ammonia it’s
Iodide