Chemical Bonding & Lewis Dot Structures I. Covalent & Ionic bonding A. chemical bonding – 1. octet rule – chem compounds tend to form so that each atom (gain e-, share e-, lose e-) has an octet (8) of electrons in its highest occupied E-level.( or have a noble gas configurations) [why??? because nature favors a lower PE & atoms have lower PE when bonded---the bond length between 2 bonded atoms is the distance between the atoms when the PE is the least---this PE is the bond energy or how much E is required to break the chem bond chart p.168 pm = picometer = 10-12m] 2. attractions between nuclei & valence e- of dif. atoms that hold atoms together 3. atoms bond & redistribute their valence eto make the atoms more stable 4. types of bonds a. ionic bonds b. covalent bonds —polar covalent & nonpolar covalent c. metallic bonds d. hydrogen bonds 5. How to determine if a bond will be ionic, polar covalent, or nonpolar covalent a. look at the electronegativity chart!!! p. 162 & p.151 1) Bonding between atoms of dif. elements is rarely purely ionic or purely covalent. It usually falls somewhere in between the 2 extremes depending on how strongly the atoms of each attract electrons ….their electronegativity. 2) look at differences in electroneg. to determine type of bond (p. 151) a) difference from 0 to 0.3 = nonpolar covalent bond (p.162) b) difference from 0.3 to 1.7 = polar covalent bond c) difference from 1.7 to 3.3 = ionic bond d) the atom with the larger electroneg. will be the more negative atom B. Covalent bonding – sharing electron pairs between 2 atoms—a molecule is produced -1. molecules – produced by covalent bonds between atoms a) diatomic molecules – contain only 2 atoms ex: O2, N2, H2 b) chemical formula – shows #’s & kinds of atoms in a compound using element symbols & subscripts 2. nonpolar-covalent bond – “pure”covalent bond where the electrons are shared equally so there is an even distribution of e3.polar covalent – covalent bond where there is an unequal attraction for the shared electrons….which means one end of the molecule is slightly more neg. δ- & the other end is slightly more positive δ+ 4. octet rule applies to most there are exceptions a) less than an octet – H (2), Be (4), B (6) b) more than an octet – SF6, PCl5 c) odd # of electrons – NO (5 + 6 = 11) 5. characteristics of covalent cmpds a) low melting & boiling pts b) most are rubbery, powdery, liquids or gases c) does not conduct electricity d) polar molecules dissolve in other polar molecules e) nonpolar molecules dissolve in nonpolar molecules 6. single bond – sharing 1 pair of electrons (short bond length) 7. double bond – sharing 2 pr of ebetween 2 atoms (shorter bond length) 8. triple bond – sharing 3 pr of ebetween 2 atoms (shortest bond length) C. Ionic bonding—transfer of electrons from one atom to another 1. ionic compound -- made of pos & neg ions that are combined so # of pos & neg charges are equal 2. formula unit – shows the types & # of ions in an ionic cmpd ( pos. ion = cation- always goes first) 3. ions reduce PE by combining in crystal formations 4. to compare bond strengths – lattice E– E released when 1 mole of gaseous ions form into a solid crystal structure 5. characteristics of ionic cmpds a) high melting & boiling pts b) exist as crystals that are brittle, shifting the structure (striking it) will cause cleavage (break along patterns) c) many are soluble in water d) conduct electricity when dissolved or melted 6. polyatomic ion – charged group of covalently bonded atoms – has both ionic & molecular char.--- they combine with other ions to form ionic cmpds D. Metallic bonding—chem bonding between metals that results from the attraction between metal atoms & the SEA of esurrounding them – the bonding is the same in all directions 1. in metals the highest E level has very few e2. the vacant p (& d) orbitals overlap 3. this allows the valence e- to roam freely throughout the entire metal a) this allows for great conductivity of heat & electricity b) small distances between orbitals allow for a wide range of photons to be absorbed easily (& re-emitted easily in the form of light which makes metals shiny) c) since bonding is same in all directions (metals don’t break easily) metals are malleable (able to be hammered into sheets) & ductile (able to be pulled into thin wires) d) very high melting & boiling pts. 4. heat of vaporization – measure of bond strength – the amt of heat required to vaporize metal into individual metal atoms in the gaseous (vaporized) state E. Other types of bonds (weaker) 1. Hydrogen bonding – intermolecular attractions that occur between polar covalent molecules that have a hydrogen atom bonded to an extemely electroneg. atom (N, O, F)—the H atom will be δ+ and be attracted to the δ(unshared pair of e-) of another like molecule a) this accounts for the high boiling pt of H2O, HF, NH3 2. London Forces – due to the constant motion of emomentary polarity occurs in all atoms and molecules (distribution of euneven) this can weakly hold atoms/molecules together a) the larger the atomic/molar mass the greater the attraction & the greater London forces can increase the bp II. Electron Dot Notation A. electron configuration that shows how the valence e- are arranged around an atom ……shown usually as dots 1. ex: p. 170 III. Lewis Structures A. electron dot notation can be used to show electron config for atoms & molecules (& ionic cmpds) *fill in dots in counterclockwise & in singles p.170 B. Lewis structures keep the dots to show unshared e- & use a line to show a shared pair of electrons 1. structural formula - shows only the shared pair of e- (p.171) Lewis Structures -- atoms: Sodium: Na. Sodium ion: Na+ Phosphorus: Bromine: ============================= ============ Ionic Compound Lewis Structure Examples: Bromide ion: We need the brackets to show that the bromide ion "owns" all of the electrons rather than sharing them. This is particularly important when we make an ionic compound such as sodium chloride. Sodium chloride: NaCl bromide: KBr Potassium Aluminum chloride: AlCl3 ======================= =========== Covalent Compound Lewis Structure Examples: Water H2O NH3 Ammonia Ammonium ion NH4+ CH4 Methane Hydrogen sulfide H2S CO2 Carbon dioxide Carbon monoxide Choosing a Bond Type - Lewis Structure Examples: Barium iodide check electronegativity difference ….formula? According to electronegativity dif. It should be polar covalent…..it’s not, it’s ionic! ionic: pos cation goes first BaI2 nonmetal to nonmetal = covalent! nonmetal to metal = ionic! Carbon disulfide check electronegativity difference….formula? covalent: less electronegative element goes first CS2 Arsenic triiodide check electronegativity difference….formula? covalent: AsI3 Hydrogen selenide check electronegativity difference….formula? covalent: H2Se Oxygen difluoride check electronegativity difference….formula? covalent: OF2 ======================= ============= Multiple Bonds - Examples Carbonate ion : CO32- However, other equally symmetrical structures are possible, so: This is called resonance IV. Molecular Geometry A. VSEPR theory– “vesper”stands for: Valence – Shell—Electron – Pair – Repulsion Theory 1. model for determining molecular geometry which relies on one simple principle: electrons repel one another. 2. in every molecular structure the electron pairs on the central atom, whether shared in bonds or unshared ("lone pairs"), will distribute around the central atom so as to be as far apart as possible. It's important to keep in mind that it is the electron pairs on the central atom that are doing the repelling and generating the shape, not the electrons on the atoms attached to the center. 3. How to find geometry: a) Draw the Lewis structure for the molecule. b) Count the number of atoms that are “stuck” to it. (don’t count the number of bonds!) c) Count lone pairs of electrons that are “stuck” to it. (don’t count the number of bonds!) IMPORTANT: This does NOT mean to count the number of lone pairs on all of the atoms in the molecule. Lone pairs on other atoms aren't important what's important is only what's directly stuck to the atom you're interested in.