Chemistry Chapter 5

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The Periodic Table Chemistry Chapter 5

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Chemistry Chapter 5. The Periodic Table. Sept 1860, group of chemists met in Germany to review scientific matters & coming to consensus about: measurement of atomic masses determining composition of compounds using atomic masses - PowerPoint PPT Presentation

Transcript of Chemistry Chapter 5

Page 1: Chemistry Chapter 5

The Periodic Table

ChemistryChapter 5

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Sept 1860, group of chemists met in Germany to review scientific matters & coming to consensus about:measurement of atomic massesdetermining composition of

compounds using atomic masses

Cannizzaro presented method for measuring mass & scientists agreed upon the std values for atomic masses

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in 1869, Dmitri Mendeleev used Cannizzaro’s method for measuring relative masses of atoms in textbook he wrote

published the arrangement of elements in – periodic table

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only 60 elements known at this time

organized elements acc to properties & new atomic masses on cards

“game of patience”Mendeleev grouped elements according to incr atomic mass & noticed certain properties appeared at regular intervals- periodic

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in 1871, Mendeleev predicted properties of elements that weren’t even discovered at that time!

not all elements fit in according to increasing atomic mass:I & Te Ar & K Co & Ni

Mendeleev couldn’t explain whyother scientist accepted the

periodic table & considered him the Father of the Periodic Law

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in 1913, Henry Moseley discovered patterns w/ x-ray tubes that led to atomic number (ch 3 notes)

he noticed that when he reordered elements on table acc to incr atomic number they fit into their patterns in better way

led to the Modern periodic table

periodic law- phy & chem properties of the elements are periodic functions of the atomic #

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Getting Acquainted

With the Periodic Table

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valence e- same for all elements in group

group 1: Alkali metals e- conf: ns1

group 2: Alkaline Earth metalse- conf: ns2

groups 3-12: Transition metalse- conf: (n-1)d1ns2

Group Properties

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groups 4-11 deviations occursum of outer s & d e- equal to group

#

group 13: ns2np1

group 14: ns2np2

group 15: ns2np3

group 16: ns2np4

group 17: Halogens ns2np5

group 18: Noble gases ns2np6

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noble gases have 8 valence e-

have stable octet very stable & unreactive

f-block elementslanthanides- rare earth metals 1st row

actinides- all radioactive; most synthetic

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phy & chem properties vary in periodic fashion

properties arise from e- configuration

5 properties:

Periodic Properties

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½ distance betw nuclei of identical atoms joined in a molecule

e- occupy large region around nucleus & size atom varies

periodic trends- gradual decrease in radii across periodsdue to increasing pos chrg of nucleus

(pulled tighter by nucleus)

1. Atomic Radii

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group trends: as go down group, atomic radii increases due to addition of e- to larger orbitals in higher energy levels

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minimum amount of energy required to remove the most loosely bound e- from an isolated gaseous atom to form an ion w/ a +1 charge

if enough energy is supplied, e- can be removed from atoms

ex: 1st IE for Ca is 590 kJ/mol

Ca + 590kJ/mol Ca+ + e-

2. Ionization Energy

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ionization- process that results in the formation of ion

2nd IE is 1145kJ

IE2 > IE1ALWAYS more difficult to remove additional e- from positive ion

IE measures how tightly e- are bound to atoms

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low IE indicates ease of e- removal & cation formation

group trends: as atomic radii increases in a group, 1st IE decreases b/c the valence e- are further

from nucleus “shielding effect”

period trends: IE incr from L to R due to increasing nuclear charge which holds e- tighter

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nonmetals tend to have higher IE than metals

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amount of energy involved in the process in which an e- is added to an isolated gaseous atom to produce an ion w/ a -1 charge

many atoms readily add e- & release energyex: Cl + e- Cl- + energy

(exothermic)

Why?

3. E- affinity

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some have to be forced to gain e- by the addition of energyBe + e- + energy Be-

period trends: group 17 elements gain e- most easily ( large neg values) reason for the reactivity of these halogens

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exceptions are seen betw groups 14 & 15 b/c ½ filled sublevels are a little more stable than ones not ½ full

group trends: generally more difficult to add e- to larger atoms than to smaller atoms

elements w/ very negative EA gain e- readily to form anions (ions w/ neg chrg)

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more difficult to add e- to an anion so 2nd EA are all positive

cation- positive ionanion- negative ion

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½ the diameter of an ion in a chemical compound

formation of a cation leads to a decrease in radius due to the e- cloud being drawn inward as valence e- are removed

formation of anion leads to an increase in radius as additional e- repel one another

4. Ionic radii

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periodic trends- metals form cationsnonmetals form anions

group trends- IR increases down group Why?

as you add higher energy levels, radius of ion incr

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chemical compounds form b/c e- are lost, gained, or shared to bring an atom to a stable octet

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measure of the power of an atom in a chemical compound to attract e-

valence e- hold atoms in compound together & properties of compound are influenced by conc of neg chrg closer to one atom than another

ex: NaCl

5. Electronegativity EN

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numerical values assigned to indicate the tendency of atom to attract e-

Fluorine – most EN element & assigned value of 4

periodic trends- gradual incr in EN from L to R across period

nonmetals tend to be more EN than metals

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groups 1 & 2 least EN elements

halogens are most EN elements

group trends- EN either decreases down group or remains similar

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