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This chapter explores the history and development of the Periodic Table, beginning with the pivotal 1860 meeting of chemists in Germany who established standard atomic masses. Dmitri Mendeleev's innovative grouping of elements by atomic mass laid the foundation for the periodic law and predicted undiscovered elements. The chapter further delves into Henry Moseley's contributions in 1913, reshaping the table based on atomic number. It examines group properties, periodic trends in atomic radii, ionization energy, electron affinity, ionic radii, and electronegativity, highlighting the significance of electron configuration in determining chemical properties.
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ChemistryChapter 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 • Cannizzaro presented method for measuring mass & scientists agreed upon the std values for atomic masses
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
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
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 why • other scientist accepted the periodic table & considered him the Father of the Periodic Law
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 #
Group Properties • valence e- same for all elements in group • group 1: Alkali metals • e- conf: ns1 • group 2: Alkaline Earth metals • e- conf: ns2 • groups 3-12: Transition metals • e- conf: (n-1)d1ns2
groups 4-11 deviations occur • sum 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
noble gases have 8 valence e- • have stable octet very stable & unreactive • f-block elements • lanthanides- rare earth metals 1st row • actinides- all radioactive; most synthetic
Periodic Properties • phy & chem properties vary in periodic fashion • properties arise from e- configuration • 5 properties:
1. Atomic Radii • 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 periods • due to increasing pos chrg of nucleus (pulled tighter by nucleus)
group trends: as go down group, atomic radii increases due to addition of e- to larger orbitals in higher energy levels
2. Ionization Energy • 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-
ionization- process that results in the formation of ion • 2nd IE is 1145kJ • IE2 > IE1 • ALWAYS more difficult to remove additional e- from positive ion • IE measures how tightly e- are bound to atoms
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
3. E- affinity • 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 energy • ex: Cl + e- Cl- + energy (exothermic) • Why?
some have to be forced to gain e- by the addition of energy • Be + e- + energy Be- • period trends: group 17 elements gain e- most easily ( large neg values) reason for the reactivity of these halogens
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/ negchrg)
more difficult to add e- to an anion so 2nd EA are all positive • cation- positive ion • anion- negative ion
4. Ionic radii • 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
periodic trends- metals form cations • nonmetals form anions • group trends- IR increases down group Why? • as you add higher energy levels, radius of ion incr
chemical compounds form b/c e- are lost, gained, or shared to bring an atom to a stable octet
5. Electronegativity EN • 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 negchrg closer to one atom than another • ex: NaCl
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
groups 1 & 2 least EN elements • halogens are most EN elements • group trends- EN either decreases down group or remains similar