13.1 First-row d-block elements Flashcards

1
Q

Electron configuration of Cr and Cu

A
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2
Q

Trend of atomic radii in d-block

A

Radius decreases across period due to inrease in charge of nucleus

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3
Q

Eelectron configurations in d block elements

A
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4
Q

Why is the decrease in atomic radii relatively small across d block?

A

Because there is small increase in effective nuclear charge experienced by 4s electrons

Addition of proton (in nucleus) - small effect as another e in 3d is added

This similarity leads to ability to form alloys in d block: one atom can be replaced with another without large disruption of the structrue

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5
Q

Common physical properties of d block elements

A
  • high electrical and thermal conductivity
  • high melting point
  • malleable (easily beaten into shape)
  • high tensile strength (can hold large loads without breaking)
  • ductile (can easily drawn into wires)
  • some ferromagnetic (Fe, Co, Ni)

Explained: strong metallic bonding, 3d and 4s electrons are close in E - involved in bonding - form delocalised sea of e - large number -> strong bonding

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6
Q

Common chemical properties of d block elements

A
  • form complexes with more than one ox number
  • form variety of complex ions
  • form coloured complexes
  • act as catalysts
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7
Q

Which metal in d block is not cinsidered a transition metal?

A

Zn

  • does not form coloured complexes/solutions
  • does not display common physical, chemical characteristics of transition metals
  • only +2 ox state

Because: different e configuration - Zn+2 ion has complete d sub-level while other transition metals don’t

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8
Q

Why are ox numbers variable in transition metals?

A

Because of ionisation energies patterns

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9
Q

Facts about transition metals

A
  • all have +2 and +3 ox numbers
  • M+3 - stabel state from Sc to Cr
  • M+2 - stable state from Mn to Cu (increase nuclear charge makes it difficult to remove 3rd e)
  • max ox state at Mn+7
  • ox states above +3 show covalent character (large charge density)
  • compounds with higher ox states - tend to be oxidising agents (ex: K2Cr2O7)
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10
Q

Define complex ion

A

COMPLEX ION: an ion formed when central atom is surrounded by ions/molecules which have a lone pair of e

Surrounding species - ligands - attached in coordinate bonds

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11
Q

How transition metals form complex ions

A

Transition ions in solutions have high densities - attract water - coordinate bonds with +ive transition ions

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12
Q

Define coordination number

A

COORDINATION NUMBER: the number of coordination bonds formed between the ligands and the central ion

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13
Q

Common complex ions, ox state, shape

A
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14
Q

Define polydentate ions

A

POLYDENTATE IONS: ions which have more than one lone pair of e available to form coordinate bond with a central transition metal ion

Example: EDTA4- - can attach 6 transition ions - hexadentate ligand

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15
Q

Define chelate

A

CHELATE: coordination/complex compound which consists of a central metal atom attached to a ligand to from cyclical/ring structure

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16
Q

Why transition metals can be catalysts

A

E configuration - free orbitals to place electrons and speed the reaction

3d and 4s e form weak bonds with reactants - effective catalysts - provide surface to come together in correct orientation

Examples:

  • Fe in Haber process
  • Ni in conevrsion of alkenes to alkanes
  • MnO2 in decomposition of H2O2
  • V2O5 in contact process
17
Q

Define heterogenous catalyst

A

HETEROGENOUS CTALYST: a catalyst which is in a different state from reactants

catalyst - solid, reactants - gaseous

18
Q

Define homogenous catalyst

A

HOMGENOUS CATALYST: catalyst in the same state fo matter as the reactants

Mix well with reactants - common in human body

19
Q

Why transition metals are homogenous catalysts

A

Because have mutiple ox states

Examples:

  • Fe2+ in heme
  • Co3+ in vitamin B12
20
Q

How magnetic properties are created?

A

Each e has its own spin - cancelled out by pairing of another e - in transition metals not all e in shells paired - magnetic properties

21
Q

Define diamagnetism, paramagnetism, ferromagnetism

A

DIAMAGNETISM: property of all materials to produce a weak opposition to applied magnetic field

PARAMAGNETISM: property of substances which have an unpaired e - stronger than diamagnetism (produces magnetisation proportional to the applied field in the same direction)

FERROMAGNETISM: property to produce magnetisation sometimes of greater magnitude than the applied field (strongest effect of all)

22
Q

Ferromagnetic tranistion metals

A

Fe, Co, Ni - unpaired d e

23
Q

Transition metal complexes are paramagnetic

A

Show paramagnetic properties because of unpaired e - pulled into magnetic field

Paramgnetism increases with the number of unpaired e; max at Cr - decreases; Zinau - no unpaired e - only diamagnetic