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Topic 12: Organic Chemistry Key Term Definition and facts 1. Organic compounds Compounds of carbon ( C ) 2. Properties of carbon atom Four (4) valance electrons Must form 4 covalent bonds Key examples CH4 , CH3CH2OH, and CH3Cl are organic compounds . . C . . I –C– I Can form single (–) , double (=) or triple (=) covalent bond Can join together to form long chains and rings Bonds easily with other nonmetals such as H, O, N and the halogens 3. Properties of Organic Compounds C–C -C-C-C- C chain C C–C ring C- C – OH Properties are due in parts to properties of C Type of substance Molecular (covalent) Bonding Covalent bonding Intermolecular force Weak Melting and Boiling points Lower than ionic and metallic (due to weak intermolecular forces) Stability under heat Decomposes easily Electrolyte Nonelectrolytes (except organic acids) Reactions Slow (due to strong covalent bond) Solubility Most are insoluble in water . 1 Topic 12: Organic Chemistry Key Concept Definition and facts 4. Names of organic Organic compounds are named with compounds prefixes (beginning) and suffixes (ending) Key examples But prefix 5. Organic Prefixes Depends on the number of C atoms in (See Table P pg 152) the substance # of C atoms Prefix # of C atoms Prefix 1 meth 6 2 eth 7 hept 3 prop 8 oct 4 but 9 non 5 pent 10 dec 6. Organic suffixes (see Table below) Class of compound Propene is an organic compound with 3 carbon atoms Heptanone is an organic compound with 7 carbon atoms Depends on the class of the organic compound Suffix (name ending) Alkanes Alkenes Alkynes Alcohols Ethers Aldehydes Ketones Organic acids Esters Amines Amides Halides are named with a 2 hex -ane -ene -yne -ol -yl ether -al -one -oic -oate -amine -amide Prop Heptan prefix. Example: is an alkene is a ketone butane Topic 12: Organic Chemistry Key Concept 7. Homologous Series Definition and facts Groups of related compounds in which each member differ from the previous by a set number of atoms. C2H6 and C3H8 are in the same homologous series Examples 8. Hydrocarbons Compounds containing only Hydrogen (H) and Carbon (C) alkanes, alkenes, and alkynes 9. Saturated hydrocarbon (alkanes) All single bonds Single covalent bond contains 2 electrons (1 pair of shared electrons) 10. Unsaturated hydrocarbon (alkenes and alkynes) Double bonds (alkene) C: :C C=C A double covalent bond 4 edouble contains 4 electrons (2 pairs of 2 pairs e- bond shared electrons) C . .C C–C 2 e1 pair e- single bond . . Triple bonds (alkynes) C: : C C = C A triple covalent bond triple contains 6 electrons (3 pairs of 6 e3 pairs e- bond shared electrons) 11. Alkanes hydrocarbons CnH2n+2 (general formula) Single bonds between C atoms (see Table Q) name endings 12. Alkenes hydrocarbons C3H6 H H H I I I H–C –C=C–H I H 1- Prop CnH2n (general formula) One double bonded C atoms (see Table Q) name endings 13. Alkynes hydrocarbons (see Table Q) C3H8 H H H I I I H–C –C–C–H I I I H H H Prop C3H4 H I H–C –C =C–H I H 1-Prop CnH2n-2 (general formula) One triple bonded C atoms name endings . 3 Topic 12: Organic Chemistry Key Term Definition and facts Key examples 14. Functional Group An atom (other than H) or a group of atoms attached to a hydrocarbon chain. -OH, -Cl, and -Oare examples of functional groups 15. Functional Group Compounds Use Table R below to classify, name, and draw functional group compounds Pay attention and note the functional group in each example below 4 Topic 12: Organic Chemistry Key Term 16. Isomers Definition and facts Organic compounds with same molecular formula but different structural formulas Key examples CH3CH2CH2Br (1-bromopropane) and Isomers MUST have: CH 3 CHBrCH3 Same molecular formula (2-bromopropane) Same number of atoms are isomers Same percent composition Same number of bonds As number of C atoms increases, the number of possible isomers also increases. 17. Alkane isomers Structural formula Condense formula molecular formula 18. Alkene isomers pentane 2,2– dimethyl propane H H H HH H CH3 H H –C–C–C–C–C–H H– C – C – C – H H H HH H H CH3 H I I I I I I I I I I CH3CH2CH2CH2CH3 I I I CH3C(CH3CH3)CH3 C5H12 butene (1-butene) 2-butene H H I I I I C5H12 I I H I H –C=C–C–C–H 19. Alkyne isomers I I H I I H–C–C=C–C–H I I I I H H HH H H H H H CH2CHCH2CH3 CH3CHCHCH3 C4H8 C4H8 pentyne (1-pentyne) H H H I I I H –C–C–C–C=C–H I I I H H H CH3CH2CH2CCH3 2-pentyne H H I I H I H–C–C–C=C–C–H I I I H H H CH3CH2CCCH3 C5H12 C5H12 . 5 Topic 12: Organic Chemistry Key Concept 20. Halide isomers Examples 1-bromopropane H H I I I I H H H I H –C –C–C–H I Br H 21. Alcohols isomers 2-bromopropane H H CH3CHBrCH3 C3H7Br C3H7Br 1-butanol H H I 2-butanol H H I I I H H H H I I H H I I I I I H – C– C – C – C–H I H H CH3CH2CH2CH2OH I I I H H OH H CH3CH2CH(OH)CH3 C4H9OH C4H9OH methyl methyl ether Ethanol (dimethyl ether) H H I I I I H H H–C–O–C–H H H I I H – C – C –OH I I H H CH3 O CH3 CH3CH2OH C2H6O C2H6O methyl propanoate ethyl ethanoate (ethyl acetate) H H O I I I I II H I H–C–C–C–O–C–H H H I H CH3CH2COOCH3 C4H8O2 6 I I CH2BrCH2CH3 I 23. Ester Isomers I I H Br H H – C – C – C– C –OH 22. Ether and Alcohol isomers I I H–C–C–C–H H O I II H H I I I I H–C–C–O–C–C–H I H H H CH3COOCH2CH3 C4H8O2 Topic 12: Organic Chemistry Key Concept 24. Ketone and aldehyde isomers Examples propanone propanal H O H H H O I II I I I I I H–C–C–C–H I I H II H–C–C–C–H H H CH3 COCH3 H CH3CH2CHO C3H6O C3H6O The following structures are not isomers of each other 25. Organic acid methanoic acid ethanoic acid (acetic acid, vinegar) O H II H –C–OH O I II H – C – C – OH I H HCOOH 26. Amine and amide ethanamine CH3COOH butanamide H H I I I I H–C–C–NH2 H H CH3CH2NH2 H HH O I I I I I I II H–C–C–C–C–NH2 H H H O II CH3CH2CH2CNH2 27. Primary alcohol The C atom with OH is bonded to one other C atom -C–C–C– I OH 28. Secondary alcohol The C atom with OH is bonded to two other C atoms -C –C –C– I OH 29. Tertiary alcohol The C atom with OH is bonded -CI -C –C–C– I OH propanol 2-propanol I to three other C atoms 2-methyl,2-propanol . 7 Topic 12: Organic Chemistry 29. Organic reactions summary Table Use for a quick review and comparing of organic reactions 8 Topic 12: Organic Chemistry Reactions Example equations When studying the organic reaction equations below, pay attention to how the products of each reaction is formed from the given reactants. You are often asked to predict a reactant or a product of a reaction. 30. Substitution replacing H with halogen 31. Hydrogen Addition (hydrogenation) adding H atoms to a double bond 32. Halogen Addition (halogenation) adding halogens to a double bond . 9 Topic 12: Organic Chemistry Reactions Example equations 33. Esterification making an ester 34. Condensation Polymerization joining by removing water For the organic reactions below, just memorize the the equation that is given for each type of reaction 35. Addition Polymerization joining without removing water 36. Saponification making soap 10 Topic 12: Organic Chemistry Reactions Example equations 37. Fermentation making alcohol 38. Combustion O2 burning could be any organic compound . 11