DM Flashcards

1
Q

electronic configuration of chromium

A

lower energy given by putting one electron in each 3d and 4s orbital, rather than 2 electrons in 4s

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2
Q

electronic configuration of copper

A

lower energy given by putting 2 electrons in each 3d orbital and one electron in 4s, rather than 9 electrons in 3d and 2 in 4s

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3
Q

transition metals form ions by losing electrons first from

A

the 4s orbital

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4
Q

transition metals forming ions

A

form one or more stable ion which have INCOMPLETELY FILLED D-ORBITALS

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5
Q

zinc and scandium as transition metals

A

often not considered transition metals
zinc only forms Zn (II) which has full d-orbitals
scandium only forms Sc (III) which has empty d-orbitals

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6
Q

potassium manganate (VII)

A

purple compound

can oxidise Fe (II) to Fe (III)

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7
Q

catalyst

A

alters rate of chemical reaction but remains chemically unchaged in the process

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8
Q

transition metals as catalysts

A

it is the availability of 3d and 4s electrons and the ability to change oxidation state that help make transition metals good catalysts

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9
Q

heterogeneous catalysis

A

catalyst in different physical state to reactants

transition metals can used 3d and 4s electrons to form weak bonds to reactants (chemisorption)

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10
Q

homogeneous catalysis

A

catalyst in same physical state as reactants

usually involves in transition metal ion forming an intermediate compound with one or more reactants

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11
Q

reaction of Fe (II), Fe (III) and Cu (II) with ammonia solution and NaOH

A

form copper (II) hydroxide, iron (II) hydroxide and iron (III) hydroxide

if source of OH- is ammonia solution, the copper (II) hydroxide precipitate will redissolve on addition of excess ammonia solution to form a purple-blue solution

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12
Q

effect of ligands on colour of compounds

A

there are 5 d orbitals in d-block metals

ligands cause these orbitals to split in such a way that some are slightly higher in energy level than other
the deltaE between the two levels is now such that the light absorbed falls in the visible part of the spectrum

transmitted light is the light that is not absorbed, and is the colour seen

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13
Q

monodentate ligand

A

can only form one dative/coordinate bond to central metal ion (eg. halides, cyanide, hydroxide)

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14
Q

ligands

A

negatively charged ions or neutral molecules possessing a lone pair of electrons
attach themselves to the central metal ion by using a lone pair of electrons to form a dative/coordinate bond
cause the five d orbitals to split into different energy levels

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15
Q

effect of concentration of solution on the light it absorbs and the colour it appears

A

more concentrated solution, more light absorbed, darker colour of solution

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16
Q

colorimetry

A

used to determine concentration of substance
narrow beam of white light passed through coloured filter
colour of filter must correspond to the colour of light most strongly absorbed (complimentary to colour of light emitted/seen)

17
Q

potential difference

A

a measure of how much each electrode is tending to accept/release electrons
measured in Volts
one volt = one joule of energy tranferred per coulumb of charge

18
Q

Ecell

A

the potential difference in an electrochemical cell when no current flows
difference in the elctrode potential of each half cell

19
Q

more positive electrode potential of half cell

A

greater tendency to accept electrons (be reduced)

20
Q

more negative electrode potential of half cell

A

lesser tendency to accept electrons

21
Q

purpose of salt bridge between half cells

A

carry current between half cells

complete circuit

22
Q

standard hydrogen half cell

A
used as a reference, all other half cells measured against it
standard conditions (1 moldm-3 solution of H+ , 298K, platinum electrode, hydrogen gas bubbled into solution)
23
Q

when no metal in half reaction, a electrode which is

A

unreactive is used (eg. platinum)

24
Q

rust

A

a hydrated form of iron III oxide > Fe2O3.xH2O

25
Q

process of rusting

A

when a water droplet is left in contact with iron/steel, the conc of dissolved oxygen in the water droplet determines which regions of the metal surface are sites of red or ox
at centre of droplet, oxygen conc is low so iron is oxidised
at edges of droplet, conc of dissolved O2 is higher, so oxygen is reduced to OH using electrons from oxidation of iron
Fe (II) and hydroxide react to form iron (II) hydroxide
iron (II) hydroxide is oxidised to hydrated iron (III) oxide

26
Q

rusting equations

A

Fe (s) Fe (II) (aq) + 2e- [NEGATIVE ELECTRODE]

1/2(O2) (g) + H2O (l) + 2e- 2OH- (aq) [POSITIVE ELECTRODE]

27
Q

sacrificial protection of iron

A

use metals with more negative electrode potential (eg. Zn or Cr)
sacrificial metal is oxidised so that iron is not, preventing formation of Fe (II)

28
Q

complex

A

central metal atom/ion surrounded by ligands

may have a +ve charge, -ve charge or no charge

29
Q

charged complex =

A

complex ion

30
Q

coordination number

A

number of bonds from the central ion to its ligands

31
Q

shapes relating to coordination number

A

6 - octahedral
4 - tetrahedral (sometimes square planar)
2 - linear

32
Q

ligand substitution reaction

A

ligands can displace other ligands
this occurs if the new complex formed is more stable than the previous complex
therefore, stability of complex is dependent on its ligands