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Published byEugenia Wheeler Modified over 9 years ago
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Electromagnetic spectrum - made of electromagnetic radiation (forms of energy that exhibit wavelike behavior as they travel through space). Electromagnetic waves - combination of electrical and magnetic fields which travel at the speed of light c = 3.00 x 10 8 m/sec
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Wavelength λ (lambda) – usually measured in nm or Ångstroms (Å)
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Frequency ν (Greek letter nu) (or f) – units are usually cycles/sec, sec –1, or Hertz (Hz).
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www.atmos.washington.edu/~hakim/301/handouts.html
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The emission of electrons from a metal when light shines on the metal. The number of electrons and their energies depends on the brightness of the incident light. http://www.astro.virginia.edu/class/oconnell/astr30/im/photoelectric-effect-2.jpg
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He suggested that the object emits energy in small, specific amounts called quanta. A quantum is the minimum quantity of energy that can be lost or gained by an atom. He proposed E = h ν where E = energy in Joules, ν = frequency, and h = Planck’s constant; 6.626 x 10 -34 J·s E = h ν
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James Prescott Joule A Joule is the derived unit of energy in the SI system. It is the energy exerted by a force of one Newton acting to move an object through a distance of one meter. I Joule = Force x distance = 1 Newton-meter = (mass x acceleration) x meter= kg· m/s 2 m = kg · m 2 /s 2
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abyss.uoregon.edu/~js/images/wave_particle.gif
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Each particle of light carries a quantum of energy which Einstein called photons. A photon is a particle of electromagnetic radiation having zero mass and carrying a quantum of energy. For an electron to be ejected from the surface of a metal, the metal surface must be hit by a single photon possessing at least the minimum energy required to knock the electron loose (multiples of whole numbers of photons) Each metal has electrons bound to its surface with different strengths so the minimum frequencies differ with each metal.
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When an excited hydrogen atom falls back from an excited state ( a higher potential energy than it has in its ground state) to its ground state ( lowest energy state of an atom ) o r a lower energy state, it emits a photon of radiation. Δ E photon = E 2 -E 1
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The collection of narrow bands of light energy is referred to as an emission line spectrum, and the individual bands of light are called spectral lines. The concept of electron energy levels is supported by spectral lines.
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Given: E = h ν and Δ E = E 2 -E 1 combining them results in ν = Δ E = ( R H ) (1 - 1 ) h h n 2 i n 2 f Further simplification: Δ E = ( R H ) (1 - 1 ) n 2 i n 2 f
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Electrons in hydrogen atoms exist in only specified energy states. Electrons in hydrogen atoms can absorb only certain specific amounts of energy and no others. When the excited electrons in a hydrogen atom lose energy, they lose only specific amounts of energy as photons. Different photons produce different color lines as seen in a bright line- emission spectrum. The main problem was that this explanation could not explain the behavior of any other element besides hydrogen.
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The visible bands in a spectra are called the Balmer series. The UV and IR lines are called Lyman and Paschen series, respectively. Scientists expected to see a continuous spectrum. This observation of the hydrogen atom led to quantum theory.
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It is impossible to determine simultaneously both the position and velocity of an electron or any other particle. ( Δ p) ( Δ x) = h (Planck’s constant) Δ p = uncertainty in momentum Δ x = uncertainty in position
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1924 Louis de Broglie Electrons should be considered as waves confined to the space around the nucleus. http://youtube.com/watch?v=x_tNzeouHC4 Bohr applet: http://www.colorado.edu/physics/2000/quantumzone/bohr.html
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EinsteinPlanck E = mc 2 E = h ν Therefore: mc 2 = h ν [Substitute v (any velocity) for c] m v 2 = h ν [rearrange and substitute v for c in c = λν ; then solve for ν = v ] λ m v 2 = h v λ Substitute, rearrange, solve for λ = h v and simplify even further: m v 2 λ = h This is the de Broglie wavelength m v equation
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De Broglie’s equation was applicable to any object, not just atoms. The wave properties of electrons were demonstrated in 1927 by Germer and Davisson (U.S.) using diffraction by crystals. This technique is used today in electron microscopy.
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(Ψ + Ψ + Ψ ) + 8π 2 m (E-V) Ψ = 0 x 2 y 2 z 2 h 2 Ψ (psi) = wave amplitude function m = mass of electron E = energy V = potential energy x, y, and z are the coordinates in space where the equation is solved
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The solutions to his equation are known as wave functions and they describe the regions in space where there is a high probability of finding the electron at the point in space for which the equation was solved. These regions of space are called orbitals.
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Describe the properties of atomic orbitals and the properties of electrons in these orbitals. There are 4 quantum numbers, the first three of which result from the solutions to Schrödinger’s wave equation. Principal quantum number (n) – the main energy level occupied by the electron. n= 1,2,3,4,... The total number of orbitals within a given shell is equal to n 2. The total number of electrons within a given shell is equal to 2n 2.
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Values include l = 0, up to and including n-1 The letter designations originally stood for sharp, principal, diffuse and fundamental. These words were used to describe different series of spectral lines emitted by the elements. Orbital quantum number Letter designation Number of orbitals Number of electrons per sublevel 0s12 1p36 2d510 3f714
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Magnetic quantum number ( m l ) – indicates the orientation of an orbital around the nucleus. Values range from – l to + l (defines how many of each type of orbital exists) Spin quantum number ( m s ) – indicates the two possible spin states of electrons in orbitals. Values are either + ½ or – ½
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Principal quantum number Orbital quantum number Magnetic quantum number Spin quantum numbers Either clockwise (+ ½) or counterclockwise (- ½) n = 1 l = 0 (s) m l = 0+ ½, – ½ n = 2 l = 0 (s), l = 1 (p) m l = 0 m l = -1, 0, +1 + ½, – ½ + ½, – ½; + ½, – ½; + ½, – ½ n = 3 l = 0 (s), l = 1 (p), l = 2 (d) m l = 0 m l = -1, 0, +1 m l = -2, -1, 0, +1, +2 + ½, – ½ + ½, – ½: + ½, – ½; + ½, – ½ + ½, – ½ ; + ½, – ½; + ½, – ½; + ½, – ½; + ½, – ½ n = 4 l = 0 (s), l = 1 (p), l = 2 (d), l = 3 (f) m l = 0 m l = -1, 0, +1 m l = -2, -1, 0, +1, +2 m l = -3, -2, -1, 0, +1, +2, +3 + ½, – ½ + ½, – ½; + ½, – ½; + ½, – ½ + ½, – ½; + ½, – ½; + ½, – ½ + ½, – ½,; + ½, – ½; + ½, – ½; + ½, – ½; + ½, – ½; + ½, – ½; + ½, – ½
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Long hand configuration (always start with 1s) Short hand, or noble gas configuration (use the noble gas immediately preceding the element in question, put its symbol in brackets [ ], and then write out the outer shell configuration. Orbital diagram/notation configuration
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Aufbau principle : An electron occupies the lowest energy orbital that can receive it. Diagonal Rule
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orbitals of equal energy are each occupied by one electron before any orbital is occupied by a second electron, and all electrons in singly occupied orbitals must have the same spin.
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no two electrons in the same atom have the same set of four quantum numbers. The first three may be the same, but the spin must be opposite.
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http://intro.chem.okstate.edu/W orkshopFolder/Electronconfnew.html
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Boron – atomic number 5 Longhand: 1s 2 2s 2 2p 1 Shorthand: [He]2s 2 2p 1 Orbital diagram: 1s 2s 2p
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Polonium – atomic number 84 Longhand: 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 10 4p 6 5s 2 4d 10 5p 6 6s 2 4f 14 5d 10 6p 4 Shorthand: [Xe] 6s 2 4f 14 5d 10 6p 4 Orbital diagram:
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For Chromium (Cr) we would predict: 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 4 but it is actually --> 1s 2 2s 2 2p 6 3s 2 3p 6 4s 1 3d 5 For Copper (Cu) we would predict: 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 9 but it is actually --> 1s 2 2s 2 2p 6 3s 2 3p 6 4s 1 3d 10
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a group of orbitals with the same energy Examples : Chromium (24) Cr Shorthand: [Ar]4s 1 3d 5 NOT [Ar]4s 2 3d 4 Mo and W are similar Copper (29) Cu Shorthand: [Ar]4s 1 3d 10 NOT [Ar]4s 2 3d 9 Ag and Au are similar
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Paramagnetic: An atom has unpaired electrons in its electron configuration. (Look at its orbital diagram) Diamagnetic: All electrons in an atom are paired. (Look at its orbital diagram)
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Electrons will be added to, or taken away from orbitals in the following order: s, p, d, f (i.e. the “outer” or “valence” shell first) Examples : Cl - 1s 2 2s 2 2p 6 3s 2 3p 5 for Chlorine becomes 1s 2 2s 2 2p 6 3s 2 3p 6 Na + 1s 2 2s 2 2p 6 3s 1 for sodium becomes 1s 2 2s 2 2p 6
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