Chapter 7 - Periodicity Flashcards

1
Q

who came up with the periodic table and what did they do?

A
  • Mendeleev - arranged in increasing atomic mass
  • lined up elements in groups w/ similar properties
  • if properties didn’t fit he would swap them e.g. I & Te
  • left gaps for elements not discovered yet
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2
Q

how is the periodic table arranged

A
  • increasing atomic no.
  • metals vs non-metals - staircase under boron
  • groups - similar chemical properties and same no. of electrons in outer shell
  • horizontal rows - periods
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3
Q

metalloids

A
  • B
  • Si
  • Ge
  • As
  • Sb
  • Te
  • At
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4
Q

periodicity

A

repeating trend in properties of elements across periods

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5
Q

periodicity examples

A
  • electron configuration
  • ionisation energy
  • structure
  • melting points
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6
Q

trends across periods (electron config.)

A

s-sub shell fills then p sub-shell

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7
Q

blocks of periodic table

A
  • corresponds to highest energy shell:
    s-block –> grp 1&2
    p-block –> grp 13-18
    d-block –> grp 3-12
    f-block –> lanthanides & acintides
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8
Q

what’s ionisation energy

A
  • measures how easily an atom loses it’s electrons to form positive ions
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9
Q

first ionisation energy definition

A

energy required to remove one electron from each atom in one mole of gaseous atoms of an element to form one mole of gaseous +1 ions

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10
Q

factors affecting ionisation energy

A
  • atomic radius - as it increases. attraction decreases
  • nuclear charge - more protons they are, the greater the attraction
  • electron shielding - inner-shells repel - larger the atom, the more shielding, the less attraction
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11
Q

second ionisation energy

A

energy required to remove one electron from each ion in one mole of gaseous 1+ ions of an element to form one mole of gaseous +2 ions

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12
Q

trend in successive ionisation energy

A
  • it increases each time as each time an electron is removed, nuclear charge attracted to less electrons
  • large increase suggests it’s moved to inner shell - decrease in radius
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13
Q

trend in ionisation energy down a group

A

decreases, radius and shielding increases, attraction decreases so ionisation energy does

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14
Q

trend in ionisation energy across a period

A

nuclear charge increases as well as attraction, atomic radius decreases so ionisation energy increases

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15
Q

why is there a fall in ionisation energy between Be & B

A

Be fills the 2s sub-shell, B fills 2s & one 2p, this is more unstable so it loses an electron more easily, so lower ionisation energy

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16
Q

why is there a fall in ionisation energy between N & O

A

N has one electron in each 2p sub-shell
O has one 2p sub-shell w/ 2 electrons, the other 2 having one electron, this is more unstable so it loses an electron more easily, so lower ionisation energy

17
Q

Metallic bonding & structure

A

electrostatic attraction between the cations and delocalised electrons
- cations in fixed position, delocalised electrons are free to move around - forms giant metallic lattice

18
Q

properties of metals

A
  • electrical conductivity - due to delocalised electrons
  • strong metallic bonds - more delocalised electrons, stronger the bonds
  • high m.p/b.p - depends on strength of bonds, high due to lots of energy needed to overcome strong electrostatic attraction between electrons and cations
  • are not soluble
19
Q

Giant covalent structures

A

many atoms hold together by a network of strong covalent bonds

20
Q

properties of giant covalent structures

A
  • high m.p/b.p - lots of energy needed to overcome strong covalent bonds
  • insoluble as bonds are too strong to be broken by interactions with lattices
  • don’t usually conduct electricity - no delocalised electrons
21
Q

graphite

A
  • parallel layers of hexagonally attracted C atoms, have 3 bonds, so delocalised electrons
  • weak intermolecular forces between layers
  • can conduct electricity
22
Q

graphene

A
  • one layer of graphite
  • can also conduct electricity
23
Q

melting point trends across periods

A
  • increases as metallic bonds gets stronger
  • continues to increase as it reaches giant covalent structures
  • then has a large decrease when gets to simple molecules
24
Q

structure trends across periods

A
  • first giant metallic
  • then giant covalent
  • then simple molecular