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Chemistry Chapter 6 Bonding
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Electronegativity - an atom’s attraction for electrons when bound to another atom
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covalent bond - pair of electrons shared formed when electronegativity difference is < 1.67 form molecules Ex: H 2 O, NH 3 two types : polar covalent (when elements are different) nonpolar covalent (in diatomic elements) O 2, N 2 - 100% covalent due to equal electronegativity
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ionic bond - atoms bonded due to different charges (electrons transferred) formed when electronegativity difference is > 1.67 form ionic compounds Ex: NaCl, CaF 2, LiBr
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ionic compounds high melting point soluble in water conduct electricity when molten crystallize well
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Molecular Shapes electron dotanglehybrid. group 1 linear 180° no ex:NaCl
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Molecular Shapes electron dotanglehybrid. group 2 linear 180° sp ex:CaCl 2
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Molecular Shapes electron dotanglehybrid. group 13 trigonal planar 120° sp 2 ex:AlCl 3
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Molecular Shapes electron dotanglehybrid. group 14 tetrahedral 109.5° sp 3 ex:CH 4
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Molecular Shapes electron dotanglehybrid. group 15 pyramidal vary no ex:NH 3
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Molecular Shapes electron dotanglehybrid. group 16 bent vary no ex:H 2 O
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Molecular Shapes electron dotanglehybrid. group 17 Linear 180° no ex:NaCl
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Organic Chemistry Organic = carbon Organic Compounds: Alkanes Alcohols AlkenesHalogenated hydrocarbons AlkynesAlkyl side chains Organic Acids Esters Cyclic hydrocarbons
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Alkanes: hydrocarbons with single bonds (R) 1.methane 2.ethane 3.propane 4.butane 5.pentane 6. hexane 7. heptane 8. octane 9. nonane 10. decane http://hyperphysics.phy-astr.gsu.edu/Hbase/hframe.html
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methane ethane propane butane
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Alkenes - hydrocarbons with double bonds 1. 2.ethene 3.propene 4.butene 5.pentene Ex: 2-butene 6. hexene 7. heptene 8. octene 9. nonene 10. decene 1-pentene3-heptene http://hyperphysics.phy-astr.gsu.edu/Hbase/hframe.html
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Alkynes - hydrocarbons with double bonds 1. 2.ethyne 3.propyne 4.butyne 5.pentyne Ex: 1-butyne 6. hexyne 7. heptyne 8. octyne 9. nonyne 10. decyne 2-pentyne1-heptyne http://hyperphysics.phy-astr.gsu.edu/Hbase/hframe.html
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Alcohols :R-OH 1.methanol 2.ethanol 3.propanol 4.butanol 5.pentanol Or methyl alcohol, ethyl alcohol, propyl alcohol, etc… Ex: 2-butanol 6. hexanol 7. heptanol 8. octanol 9. nonanol 10. decanol 1-pentanol1-heptanol http://hyperphysics.phy-astr.gsu.edu/Hbase/hframe.html
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Alkyl sidechains Ex: methyl propane methyl butane 2 - methyl pentane 3 - ethyl heptane 2, 3, 3 - trimethyl hexane 2,3-dimethyl octane
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Halogenated hydrocarbons (alkyl halides): R-X Examples: bromomethane chloroethane 2 - fluoro pentane 1,2,3-tri chloro heptane
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O Organic acids:R - C - OH
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Cyclic compounds
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http://images.google.com/imgres?imgurl=http://www.bmrb.wisc.edu/metabolomics/standards/nicotine/lit/4007.png&imgrefurl=http://www.bmrb.wisc.edu/metabolomics/gen_metab_summary_5.php?molName=nicotine&h=300&w=300&sz=7&hl=en&start=87&um=1&tbnid=md
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Esters alcohol + organic acid -----> ester + water ------yl ----oicEx: butyl ethanoate methanol + ethanoic acid ---->methyl ethanoate propanol + ethanoic acid ---> propyl ethanoate hyperphysics website
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6th Period
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7th Period
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