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Unit 6: Organic Chemistry ,[object Object],[object Object]
Standards Covered Today: ,[object Object],[object Object],[object Object],[object Object]
Introduction ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Names of Structures ,[object Object],[object Object],[object Object],[object Object],C 6 H 14  or CH 3 (CH 2 ) 4 CH 3
Notes on Structures ,[object Object],[object Object],[object Object],[object Object],[object Object]
Isomers ,[object Object],[object Object],[object Object]
Introduction to Nomenclature of Organic Molecules ,[object Object],[object Object],[object Object],[object Object],[object Object]
Alkanes ,[object Object],[object Object],[object Object],[object Object],[object Object]
Nomenclature for compounds ,[object Object],Number of C atoms Root 1 Meth- 2 Eth- 3 Prop- 4 But- 5 Pent- 6 Hex- 7 Hept- 8 Oct- 9 Non- 10 Dec-
[object Object],[object Object]
IUPAC Naming System: Alkanes ,[object Object],[object Object],[object Object],[object Object]
Alkane Nomenclature Examples ,[object Object],3-methyl hexane ,[object Object]
[object Object],Alkyl groups are named by replacing the –ane suffix of the alkane name with –yl. E.g.  CH 3 CH 3   Ethane CH 3 CH 2 - Ethyl group CH 3 CH 2 CH 3   PropaneCH 3 CH 2 CH 2 -   Propyl group
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
3-ethyl-2,4,5-trimethylheptane
Recognizing Types of Substitution
Cycloalkanes ,[object Object],[object Object],[object Object]
Two simple rules of cycloalkanes ,[object Object],[object Object]
[object Object],1,1,3-trimethylcyclopentane ,[object Object],4-cyclopropyl-3-methyloctane
Complex Substituents ,[object Object],[object Object],[object Object]
Examples ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],3.)  (CH 3 CH 2 ) 3 CH 4.)  (CH 3 ) 2 CH(CH 2 ) 3 CH 3
Physical Properties of Alkanes ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Dispersion Forces
[object Object],[object Object],Leads to liquids, then solids More compact structure, surface area decreases Less contact between molecules, dispersion forces decrease, so lower boiling point
Try these: ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
Elements of Unsaturation ,[object Object],[object Object],[object Object],[object Object]
Propose a Structure for C 5 H 8   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Alkene Nomenclature ,[object Object],[object Object],[object Object],[object Object]
Try these: 1-butene 2-methyl-2-butene 3-methylcyclopentene 2-(1-methyl propyl)-1,3-cyclohexadiene 3-propyl-1-heptene
Geometric Isomerism ,[object Object],[object Object],trans -2-pentene cis -1,2-dibromoethene
Alkynes ,[object Object],[object Object],[object Object]
Alkyne Nomenclature ,[object Object],[object Object],[object Object],[object Object]
Try these propyne 5-bromo-2-pentyne 3-methyl-1-hexyn-5-ene
Practice Problems ,[object Object]
Agenda  ,[object Object],[object Object]
Alcohols ,[object Object],[object Object],[object Object],[object Object]
Alcohol Examples
Ether Nomenclature ,[object Object],CH 3 —O—CH 3 Dimethyl ether CH 3 CH 2 OCH 2 CH 3 Diethyl ether
Aldehydes Nomenclature ,[object Object],[object Object],[object Object]
Aldehyde Example methanal butanal 2-methyl butanal
Ketone Nomenclature ,[object Object],[object Object],[object Object]
Ketone Examples 3-pentanone propanone 3-methyl-2-butanone
Carboxylic Acid Nomenclature ,[object Object],[object Object],[object Object],[object Object],[object Object]
Carboxylic Acid Examples
Ester Nomenclature ,[object Object],[object Object],[object Object],[object Object]
Amine Nomenclature ,[object Object],[object Object],[object Object]
Functional Groups as Isomers ,[object Object],[object Object]
Try the following:

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