ALKENES AND ALKYNES Alkenes contain one or more

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ALKENES AND ALKYNES

ALKENES AND ALKYNES

 • Alkenes contain one or more double bonds • Alkynes contain one or

• Alkenes contain one or more double bonds • Alkynes contain one or more triple bonds • Since alkenes and alkynes are NOT bonded to the maximum possible number of atoms, these compounds are often referred to as unsaturated hydrocarbons Boiling points and melting points: alkynes < alkenes < alkanes Reactivity: alkynes > alkenes > alkanes

 • alkenes are used to synthesize polymers because they are reactive • alkynes

• alkenes are used to synthesize polymers because they are reactive • alkynes are very unstable. As a result, they rarely occur in nature • When naming these molecules, there a few extra rules to follow: your main chain must include double or triple bonds at lowest position number (indicate position #) when numbering the main chain, double and triple bonds have priority over alkyl groups

ALKENES (C=C): The chemical formula of alkenes follows a general formula Cn. H 2

ALKENES (C=C): The chemical formula of alkenes follows a general formula Cn. H 2 n For example: C 2 H 4 = ethene C 3 H 6 = propene C 4 H 8 = butene

Name the following: * double bonds have priority 5 4 3 2 4 -

Name the following: * double bonds have priority 5 4 3 2 4 - methyl- 2 - pentene Location of double bond 1

Name the following: 6 5 4 3 2 1 3 - ethyl-2 - hexene

Name the following: 6 5 4 3 2 1 3 - ethyl-2 - hexene * main chain must include double bond

Name the following: * 2 double bonds 1 2 3 4 5 6 2

Name the following: * 2 double bonds 1 2 3 4 5 6 2 - methyl- 2, 5 - heptadiene 7

Name the following: 5 1 2 3 6 4 2, 3, 4 - trimethyl-3

Name the following: 5 1 2 3 6 4 2, 3, 4 - trimethyl-3 - hexene

Name the following: 1 2 3 4 5 6 3 - isopropyl-1, 3 -

Name the following: 1 2 3 4 5 6 3 - isopropyl-1, 3 - hexadiene

ALKYNES (C C): The chemical formula of alkenes follows a general formula Cn. H

ALKYNES (C C): The chemical formula of alkenes follows a general formula Cn. H 2 n-2 For example: C 2 H 2 = ethyne C 3 H 4 = propyne C 4 H 6 = butyne

Name the following: * ethyl before methyl 1 2 3 4 5 6 7

Name the following: * ethyl before methyl 1 2 3 4 5 6 7 3 - ethyl-6 - methyl- 4 - octyne 8

Name the following: CH 3 C(CH 3)2 CH(CH 2 CH 3)C CH CH 3

Name the following: CH 3 C(CH 3)2 CH(CH 2 CH 3)C CH CH 3 CH 2 – CH 3 – CH – C CH 5 4 CH 3 3 2 1 3 -ethyl-4, 4 -dimethyl-1 - pentyne

Draw the following: (a) 3 -methyl-2 -pentene CH 3 – CH =C–C H 2–

Draw the following: (a) 3 -methyl-2 -pentene CH 3 – CH =C–C H 2– C H 3

Try drawing this one on your own: (b) 2, 5, 7 -trimethyl-5 -propyl-3 -octyne

Try drawing this one on your own: (b) 2, 5, 7 -trimethyl-5 -propyl-3 -octyne CH 3 CH CH 3 CH 2 CH 3

Cyclic Hydrocarbons

Cyclic Hydrocarbons

 • Cyclic hydrocarbons are hydrocarbon ring structures • When naming these molecules, the

• Cyclic hydrocarbons are hydrocarbon ring structures • When naming these molecules, the cyclic structure is always the main chain • Number the carbons, in either direction, so that the branches have the lowest possible position number • Double bonds have priority over alkyl groups • have the prefix “cyclo”

Name the following: (a) CH 3 2 3 4 5 CH 3 (b) 2

Name the following: (a) CH 3 2 3 4 5 CH 3 (b) 2 3 1 5 CH 2 CH 3 1 6 1 -ethyl- 2, 4 -dimethylcyclohexane CH 3 3, 4 -dimethyl -1 -cyclopentene 3, 4 -dimethylcyclopentene 4 CH 3 • Do not need to # double bond (it has to be between 1 & 2)

Draw the following: (a) 3, 3 -diethyl-2 -methylcyclopentene CH 3 1 5 4 2

Draw the following: (a) 3, 3 -diethyl-2 -methylcyclopentene CH 3 1 5 4 2 CH 2 CH 3 3 CH 2 CH 3 (b) 2 -ethyl-1, 4 -dimethylcyclohexane 5 4 CH 3 6 3 1 CH 3 2 CH 2 CH 3

HOMEWORK WS “Naming and Drawing Alkenes” WS “Naming and Drawing Alkynes WS “Naming and

HOMEWORK WS “Naming and Drawing Alkenes” WS “Naming and Drawing Alkynes WS “Naming and Drawing Cyclic molecules”