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Published byHilda Chambers Modified over 9 years ago
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chemical bond - force that holds groups of atoms together group function as a unit bond NRG – NRG required to break bond indicates strength of bond bond length – distance between two atoms bonded together indicates most stable(least amount of NRG) state between two atoms
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ionic bond – electromagnetic force that holds two oppositely charged ions together formed between cations and anions cations formed when metals lose e - ‘s ▪Na Na + + e - (oxidation) anions formed when nonmetals gain e - ‘s ▪Cl + e - Cl - (reduction) opposite charges attract(electromagnetic force) ▪Na + + Cl - Na + Cl -
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why do substances form ionic bonds??? lowest possible NRG for the system(substances involved with bonding) see figure 8.9 on page 355 1. change Li(s) to Li(g) endothermic Li(s) + 161 kJ/mol Li(g) 2. Li(g) oxidizes endothermic Li(g) + 520 kJ/mol Li + + e - 3. fluorine molecules separate and form fluorine atoms endothermic ½ F 2 (g) + 77 kJ/mol F(g)
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4. fluorine reduces exothermic F(g) + e - F - (g) + 328 kJ/mol 5. ionic bond formed extremely exothermic Li + (g) + F - (g) Li + F - + 1047 kJ/mol total endothermic processes = 758 kJ/mol total exothermic processes = 1375 kJ/mol NET NRG = 617 kJ/mol overall process is exothermic so an ionic bond forms
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metals lose e - (oxidation) nonmetals gain e - (reduction) ionic compound formula total oxidation = total reduction Mg 2+ F - MgF 2 utilize criss-cross method Mg 2+ F - MgF 2
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dissolving ionic crystals
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covalent bond – force of attraction between 2 atoms when e - ‘s are shared each nucleus attracts the other atoms e - ‘s balance between attraction and repulsion
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bonds result from system trying to attain lowest possible NRG state two driving forces in nature 1)lowest NRG 2)highest entropy(disorder/chaos) ionic and covalent bonds generally form to attain the lowest NRG state for atoms involved single covalent bond – 1 pair e - shared H-H, F-F, Cl-Cl, Br-Br, I-I double covalent bond – 2 pair e - shared O=O triple covalent bond – 3 pair e - shared N≡N
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molecular orbital most probable location of e - ‘s when covalently bonded
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sigma ( ) bond centers along the internuclear axis. single covalent bond pi ( ) bond occupies space above and below internuclear axis. 2 nd or 3 covalent bond
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electronegativity attraction an atom has for another atom’s e - ‘s arbitrary scale – based on F varies periodically (click here) (click here) ▪generally increases across and decreases down electronegativity difference can generally predict type of bond if diff. > 1.7 = ionic bond if 1.7 > diff. > 0.3 = polar covalent bondpolar covalent bond if diff. < 0.3 = nonpolar covalent bondnonpolar covalent bond
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nonpolar covalent bond pure covalent bond sharing of e - ‘s is equal no poles/charges created
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Lewis structures localized e - model for diagramming bonds and molecular shapes 1) total valence e - of all atoms in molecule HCl = 8 valence e - 2) write symbols for each element least number of = interior atom hydrogen is always exterior atom H Cl
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3) add a pair of e - between atoms bonding together H : Clvalence e - remaining = 6 4) add remaining e - in pairs to exterior atoms to form octets if e - remain add them to interior atoms to form octets not H, H forms duets if necessary, move e - pairs to create octets H : Cl 5) all shared pair of e - become dashes H - Cl : : : : :
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6) follow VSEPR for shape VSEPR – valence shell electron pair repulsion theory model used to predict geometry/shape of a molecule based on the repulsion of e - pairs e - pairs repel each other to maximum distance in 2-dimension = 90 o in 3-dimension = 109.5 o
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Molecular Geometry 3-dimensional shapes determine the physical and chemical properties of molecules example – sucrose- its molecular shape fits the nerve receptors of the tongue for sweetness sugar substitutes(Splenda, Nutrasweet, …) have similar shapes as sucrose 1) linear all atoms lie in a straight line HCl, CO 2
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2) bent atoms not in straight line e - pairs point to 4 corners of tetrahedron
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3) trigonal pyramidal 3 atoms bonded to central atom and a pair of nonbonding e -
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4) trigonal planar 3 groupings of e - around central atom all atoms lie in same plane
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5) tetrahedral 4 groupings of e - around central atom
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resonance ability to draw more than one acceptable shape for a molecule originally believed molecule resonated between different shapes ▪benzene, nitrate ion actual structure is an average of all resonant images
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exceptions to octet rule C, N, O, F always follow octet rule Be and B often have less than 8 3 rd period and heavier usually follow ▪ some may exceed by putting e - in unoccupied d- orbitals ▪when writing Lewis structures follow octet rule ▪if e - remain add them to elements with d orbitals
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polar molecules molecule with oppositely, partially charged atoms on opposite sides aka – dipoles, dipole moments
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molecule that has an asymmetrical distribution of charge partial charges not evenly distributed around central atom polar molecules must have: polar bonds(partial charges) unevenly distributed partial charges
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HCl H = 2.1, Cl = 3.0 (electroneg diff = 0.9) = bond is polar H = δ+, Cl = δ- linear shape polar molecule N 2 N = 3.0 (electroneg diff = 0) = bond is nonpolar nonpolar molecule
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H 2 O H = 2.1, O = 3.5 (electroneg diff = 1.4) = bonds are polar H = δ+, O = δ- bent shape polar molecule NH 3 N = 3.0, H = 2.1 (electroneg diff = 0.9) = bonds are polar H = δ+, N = δ- trigonal pyramidal shape polar molecule
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CCl 4 C = 2.5, Cl = 3.0 (electroneg diff = 0.5) = bonds are polar C = δ+, Cl = δ- tetrahedral shape nonpolar molecule
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hybridization formation of hybrid orbitals from atomic orbitals of similar NRG sp 3 hybridization
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sp 2 hybridization
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sp hybridization
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naming binary molecules 1) determine # of 1 st element ▪use prefix if more than one ▪1=mono-2=di- ▪3=tri-4=tetra- ▪5=penta-6=hexa- ▪7=hepta-8=octa- ▪9=nona-10=deca- 2) name element 3) determine # of 2 nd element ▪use prefix except if bonded to H 4) use root of element name 5) end with -ide
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polar covalent bond bond in which e - ‘s are shared unequally ▪electronegativity of one atom is higher than other
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