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Covalent Bonds (2 nonmetals) …atoms share e– to get a full valence shell C1s 2 2s 2 2p 2 F1s 2 2s 2 2p 5 *Both need 8 v.e – for a full outer shell (octet rule)!* o 4 valence e- 7 valence e- o x o o C x x x x x x F Bonding Review
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Draw the Lewis dot structure for the following elements (write e- config first): Si O P B Ar Br 1s 2 2s 2 2p 6 3s 2 3p 3 1s 2 2s 2 2p 4 1s 2 2s 2 2p 1 1s 2 2s 2 2p 6 3s 2 3p 6 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 10 4p 5 1s 2 2s 2 2p 6 3s 2 3p 2 4 valence e- 6 valence e- 5 valence e- 3 valence e- 8 valence e- 7 valence e-
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1 2 3 4 5 6 7 8 H He Li Be B C N O F Ne Na Mg Al Si P S Cl Ar K Ca Se Br Kr Rb Sr Te I Xe Cs Ba Notice any trends…? TRANSITION METALS The group # corresponds to the # of valence e –
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C F F F F Let’s bond two F atoms together… Each F has 7 v.e. and each needs 1 more e- F F F F Now let’s bond C and F atoms together… C F F F F carbon tetrafluoride (CF 4 ) F2F2
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Lewis Structures: 2D Structures NH 3 CH 2 O CO 2 SO 2 CH 4
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1.Sum the # of valence electrons from all atoms Anions: add e – (CO 3 2- : add 2 e – ) Cation: subtract e – (NH 4 + : minus 1 e – ) 2.Predict the arrangement of the atoms Usually the first element is in the center (often C, never H) 3.Make a single bond (2 e – ) between each pair of atoms 4.Arrange remaining e – to satisfy octets (8 e – around each) Place electrons in pairs (lone pairs) Too few? Form multiple bonds between atoms: double bond (4 e – ) and triple bond (6 e – ) 5.Check your structure! All electrons have been used All atoms have 8e- Exceptions: Remember that H only needs 2e – ! Drawing Lewis Structures
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Lewis Structure Practice CH 4 H 2 O NF 3 HBr OF 2 HCN NO 3 - CO 3 2- Draw a Lewis Structure for the following compounds: NHC
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NHC
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Lewis Structure Trends Here are some useful trends… C group Forms a combo of 4 bonds and no LP (Lone Pairs) e.g. CO 2 N group Forms a combo of 3 bonds and 1 LP e.g. NH 3 O group Forms a combo of 2 bonds and 2 LP e.g. CH 2 O F group (halogens) Forms 1 bond and 3 LP e.g. OF 2 Note that these are NOT always true!
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Carbonite Carbonate? CO 3 2- CO 2 2-
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Resonance Structures Resonance structures differ only in the position of the electrons The actual structure is a hybrid (average) of the resonance structures Technically NOT two single bonds and one double bond All 3 Oxygen atoms share the double bond 3 equal bonds (somewhere between a double and single) Arrow formalism: curved arrows show electron movement Show resonanceShow movement of e -
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Predicting Molecular Shape: VSEPR (Valence Shell Electron Pair Repulsion) Electrons repel each other The molecule adopts a 3-D shape to keep the electrons (lone pairs and bonded e - ) as far apart as possible Different arrangements of bonds/lone pairs result in different shapes Shapes depend on # of bonds/lone pairs (“things”) and LP around the central atom
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Selected Shapes and Geometries using VSEPR “Things”
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Carbon Dioxide: CO 2 Two “things” (bonds or lone pairs) Linear geometry 0 LP → Linear Shape 180 o Bond angle COO Lewis Structure
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C H H O Formaldehyde: CH 2 O Three “things” Trigonal planar geometry 0 LP → Trigonal planar shape 120° bond angles Lewis Structure
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Sulfur Dioxide: SO 2 Three “things” Trigonal planar geometry 1 LP → Bent shape 120° bond angles Lewis Structure S O O B A A A
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Methane: CH 4 Lewis Structure Four “things” (bonds/LP) Tetrahedral geometry 0 LP → Tetrahedral shape 109.5 o bond angles
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Ammonia: NH 3 Lewis Structure Four “things” (bonds/LP) Tetrahedral geometry 1 LP → Trigonal pyramid shape 107 o bond angles
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Water: H 2 O Lewis Structure 4 “things” (bonds/LP) Tetrahedral Geometry 2 LP → Bent Shape 104.5 o bond angle
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Hydrogen Chloride: HCl Four “things” (bonds/LP) Tetrahedral geometry 3 LP → Linear Shape No Bond angle Lewis Structure ClH
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A special note… For any molecule having only two atoms… e.g. N 2, CO, O 2, Cl 2, HBr, etc. Geometry = Linear Shape = Linear Bond Angle(s)? = None It is much like geometry… what is formed by connecting two points? …a line. NN HBr Cl OO
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You will need to commit these to memory! “Things”
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VSEPR Practice (w/o aid of yellow sheet) CO 2 G: S: Angle: ClO 2 - G: S: Angle: NO 2 - G: S: Angle: CH 3 COO - G: S: Angle: PBr 3 G: S: Angle: AsO 4 3- G: S: Angle:
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Electronegativity and Bond Type The electronegativity difference between two elements helps predict what kind of bond they will form. Bond type Covalent Polar covalent Ionic Definition e- are evenly shared e- are unevenly shared e- are exchanged (gained or lost) Electronegativity difference ≤ 0.4 0.5 – 1.8 > 1.8
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Electronegativity difference ≤ 0.4 0.5 – 1.8 > 1.8 Practice with Bond Types Bond type Covalent Polar covalent Ionic H 2.1 Li 1.0 Be 1.5 B 2.0 C 2.5 N 3.0 O 3.5 F 4.0 Na 0.9 Mg 1.2 Al 1.5 Si 1.8 P 2.1 S 2.5 Cl 3.0 Br 2.8 I 2.5 K 0.8 Ca 1.0 Sample Bonds NaCl Cl-Cl C-O C-H Electronegativity Difference 3.0 – 0.9 = 2.1 3.0 – 3.0 = 0 3.5 – 2.5 = 1.0 2.5 – 2.1 = 0.4 Bond Type? Ionic Covalent Polar covalent Covalent
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Dipole Moments and Polarity Arrow points toward partially “-” end Occurs in polar covalent bonds Uneven distribution of e - Atoms become partially charged Partially “+” charged end δ-δ- δ+δ+
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Polarity Examples HCN CO 2 CO 3 2- CH 2 O SO 2 CH 4 CH 3 F C 3 H 8 CO NH 3 1.Check molecule for dipole moments (polar bonds) 2.When determining overall polarity, an imbalanced structure will likely be polar (at least partially) 3.Even with polar bonds, a balanced structure is non-polar overall 4. Any structure with lone pairs on the central atom is automatically polar! Try these with your neighbors… Polar Non-polar Polar Non-polar Polar Non-polar Polar
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Intermolecular Forces (IMF’s) Intramolecular Forces = bonding within a molecule e.g. ionic, covalent, polar covalent bonds Intermolecular Forces = interactions between two molecules …Intercity v. Intracity v. Innercity Intermolecular Forces are ALL weaker than Intramolecular bonds
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IMF’s: Ion-Ion Force + - + + Similar Charges Repel Opposite Charges Attract Na + Cl – Na + Cl – Attractive and repulsive forces between two separate ions.
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H H H IMF’s: Ion-Dipole Force Na + Cl H δ+δ+ + δ-δ- + The interaction between an ion and another molecule that has a dipole moment. (polar covalent) O Na + Lewis Structure δ-δ- δ+δ+ δ+δ+ δ+δ+ δ-δ-
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IMF’s: Dipole-Dipole Force The interaction between two separate molecules, each having a dipole moment. (polar covalent) H Cl H H H HCl = Stomach Acid δ-δ- δ+δ+ δ-δ- δ+δ+
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IMF’s: Hydrogen Bonding A specific type of dipole-dipole interaction between an H bond donor and an H bond acceptor. H H O H H O H bond donor: an H bonded to N, O, or F H bond acceptor: any lone pair of e –
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IMF’s: London Dispersion Forces Involves an instantaneous dipole. This dipole will induce dipoles in other molecules. H H Probable? Yes Possible? Yes Probable? Yes Possible? Yes Probable? Yes Possible? Yes Probable? NO! Possible? YES! δ+δ+ δ-δ- Why instantaneous? This dipole will only remain for an instant! The electrons will quickly move to another part of the molecule! H H δ-δ- δ+δ+ H H H H H H H H H H H H Instantaneous = WEAKEST! All molecules will exhibit LDF ↑ mass,↑ LDF
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IMF Review Ion-Ion Ion-Dipole Hydrogen Bonding Dipole-Dipole London Dispersion Forces (LDFs) a.k.a. van der Waals Forces STRONGEST Weakest *Remember: These are all weaker than actual bonds (ionic, covalent, etc.). These are just attractions. Involves an ion (+ and – charged) Involves a dipole (polar molecule) Involves a non-polar molecule
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C H H O Formaldehyde: CH 2 O Trigonal planar geometry 120° bond angles Polar C=O bond = Net dipole moment IMF= Dipole-Dipole Lewis Structure IMF Practice
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Methane: CH 4 Lewis Structure Tetrahedral geometry 109 o bond angles Covalent bonds = No net dipole IMF = London dispersion forces
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Ammonia: NH 3 Lewis Structure Polar Bonds, Lone pairs = Dipole 1 H bond acceptor (LP), 3 H bond donors (N-H) IMF = Hydrogen Bonding Trigonal pyramid 107 o bond angles
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Carbon Dioxide: CO 2 Linear geometry 180 o Bond angle COO Lewis Structure C=O bond is polar, but… Dipoles cancel = No net dipole IMF = London Dispersion Forces!
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Bent Water: H 2 O Polar bonds, lone pairs = Net dipole 2 H bond acceptor (LP), 2 H bond donors (O-H) IMF = Hydrogen bonding Lewis Structure
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