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8.3 Periodic Trends in Atomic Properties, Study notes of Chemistry

– Explains the charges of the stable anions of groups 15, 16 and 17 (N3-, O2-, F- …) Page 4. • Irregularities in the electron affinity trends. – Decrease in A1 ...

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8.3 Periodic Trends in Atomic Properties
Periodicity is based on the electron configuration
which depends on the # of electrons which in turn
depends on the number of protons (atomic #)
Trends in Atomic Size
Atomic radius half of the distance between
the centers of two adjacent identical atoms
Metallic radius for metals in the solid phase
Covalent radius for nonmetals in molecules
Atomic radii increase down a group and
decrease from left to right across a period
(for main group elements)
Down a group the valence shell principal
quantum number (n) increases orbitals
and electron clouds become larger
Across a period the nuclear charge
increases while the new electrons enter the
same principal shell (do not shield each other
effectively) the effective nuclear charge
(Zeff) increases and draws the electrons
closer to the nucleus
Example: Compare the sizes of Ge, Sn and Se.
Sn is below Ge Sn>Ge
Ge is to the left of Se Ge>Se
For the transition elements, the size trend
across a period is not as pronounced because
electrons are added to inner shells which
provides better shielding of the outer
electrons, so Zeff does not increase as much
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8.3 Periodic Trends in Atomic Properties

  • Periodicity is based on the electron configurationwhich depends on the # of electrons which in turndepends on the number of protons (atomic #)

Trends in Atomic Size •^ Atomic radius

– half of the distance between

the centers of two adjacent identical atoms–^

Metallic radius

  • for metals in the solid phase -^ Covalent radius
    • for nonmetals in molecules

• Atomic radii

increase down a group

and

decrease

from left to right

across a period

(for main group elements) • Down a group

– the valence shell

principal

quantum number (

n ) increases

orbitals

and electron clouds become larger• Across a period

– the nuclear charge

increases while the new electrons enter thesame principal shell (do not shield each othereffectively)

the

effective nuclear charge

( Z

) increases eff

and draws the electrons

closer to the nucleus Example:

Compare the sizes of

Ge

,^ Sn

and

Se

Sn is below Ge

Sn>Ge

Ge is to the left of Se

Ge>Se

• For the

transition elements

, the size trend

across a period

is not as pronounced because

electrons are added to inner shells whichprovides better shielding of the outerelectrons, so

Z

eff^

does not increase as much

Trends in Ionization Energy •^ Ionization energy (

I )^

  • energy required to

remove an electron from a gas-phase atom–^

First

ionization energy (

I^ ) – to remove the 1^1

st^ e

X^ (g)

X

+^ (g)

  • e
  • -^ Second

ionization energy (

I^ ) – to remove a 2^2

nd^ e

+X

(g)

X

2+^ (g)

  • e
    • Ionization energies are positive (endothermic)and become larger with every subsequentionization

I^1

<^

I^ <^2

I^3

<^

I^4

  • It’s harder to remove an
  • e from a positive ion
  • First ionization energies

decrease down a group

and

increase

from left to right

across a period

(with some exceptions)–^

Down a group

electrons are removed from shells

that are farther from the nucleus (less tightlybound)– Across a period

Zeff

increases (valence electrons

are more tightly bound to the nucleus)

  • Low ionization energy accounts for the metalliccharacter of elements in the lower left corner ofthe table (

s ,^

d ,^

f^ and some of the

p^

block) – easy

removal of

  • e

provides better conductivity and

tendency to form cations

  • Irregularities in the ionization energy trends–

Decrease in

I^1

between groups 2(2A) and 13(3A)

elements

group 2A

n s

2

group 3A

n s

2 n p

1

  • The

n p

electron is easier to remove than the

n s

electron –

p -subshells have higher energy and

are less tightly bound

  • Decrease in

I^1

between groups 15 and 16 elements group 15(5A)

ns

2 np

1 npx

(^1) npy

(^1) z

group 16(6A)

ns

2 np

2 npx

(^1) npy

(^1) z

  • It’s easier to remove the paired electron on the^ p

-orbital – paired electrons repel each other x stronger than unpaired electrons

  • Irregularities in the electron affinity trends–

Decrease in

A^1

between groups 1 and 2 elements group 1

n s

1

group 2

n s

2

  • For group 2 the new electron is added to the higherenergy

n p

subshell

  • Decrease in

A^1

between groups 14 and 15 element (^) group 14

n s

2 n p

1 n x

(^1) py

group 15

n s

2 n p

1 n x

(^1) py n p

(^1) z

  • For group 15 the new electron is added to analready occupied

n p

orbital – pairing of electrons

is energetically unfavorable (stronger repulsion)

Groups 1, 2:Reactivemetals, formcations (low

I )

Groups 16, 17:Reactivenonmetals, formanions (high,exothermic

A )

Group 18:Noble gases,Inert (high

I

and low

A )