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The basis for organic chemistry

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Presentation on theme: "The basis for organic chemistry"— Presentation transcript:

1 The basis for organic chemistry
Hydrocarbons The basis for organic chemistry

2 Organic Compounds Contain C bonded to other elements, commonly H, O, N, S, and halogens Carbon Can form many different compounds due to its hybrid orbitals Has intermediate electonegativity, so its most likely to form molecular compounds (Recall: molecular compounds have diverse properties) Can make single, double, and triple bonds Can form isomers (same molecular formula but different arrangement of atoms)

3 Types of Hydrocarbons Saturated: Contain the maximum number of hydrogens, single bonds between all carbons Unsaturated: Contain 1+ double or triple bonds

4 Types of Hydrocarbons Aliphatic Carbons are arranged in chains
Cyclic: Carbons are arranged in rings Aromatic: Contain a benzene ring

5 Types of Hydrocarbons

6 Structural Shorthand Explicit hydrogens (those required to complete carbon’s valence) are usually left off of drawings of hydrocarbons C1 C2 C3 C4 C1 C2 C3 C4 Line intersections represent carbon atoms

7 Cyclic Alkanes Cyclopropane, C3H6 Cyclobutane, C4H8
Cyclopentane, C5H10 Cyclohexane, C6H12 Cycloheptane, C7H14 Remember, explicit hydrogens are left out

8 Hydrocarbon Root Names
# of Carbons Root Name 1 meth- 2 eth- 3 prop- 4 but- 5 pent- 6 hex- 7 hept- 8 oct- 9 non- 10 dec-

9 Naming Alkanes Based off the number of C atoms in the longest chain
Count the number of C’s in the longest chain Determine the appropriate root Add the suffix “ane”

10 Rules for Naming Alkanes (Nomenclature)
For a branched hydrocarbon, the longest continuous chain of carbon atoms gives the root name for the hydrocarbon 1 2 3 4 4 carbon chain = butane

11 Naming Branched Alkanes
Based off the number of C atoms in the longest chain Count the number of C’s in the longest chain Determine the appropriate root Use the numbered C’s to give the branches a position number add “yl” suffix Add the suffix “ane”

12 Naming Branched Alkanes
Important Rules: Start numbering from the end that will give you the lowest number of branches If there is more than one type of branch, name the branches in alphabetical order If there is more than two of the same type of branch, give the branch a position number and prefixes “di”, “tri” “tetra” etc. Put commas between numbers and hyphens between numbers and letters

13 Rules for Naming Alkanes (Nomenclature)
When alkane groups appear as substituents, they are named by dropping the -ane and adding -yl. —CH3 Methyl —CH2CH3 Ethyl —CH2CH2CH3 Propyl —CH2CH2CH2CH3 Butyl Methyl

14 Rules for Naming Alkanes (Nomenclature)
The positions of substituent groups are specified by numbering the longest chain of carbon atoms sequentially, starting at the end closest to the branching. 1 2 3 4 Methyl

15 Rules for Naming Alkanes (Nomenclature)
The location and name of each substituent are followed by the root alkane name. The substituents are listed in alphabetical order (irrespective of any prefix), and the prefixes di-, tri-, etc. are used to indicate multiple identical substituents. 1 2 3 4 Name: 2-methylbutane Methyl

16 Nomenclature Practice
Name this compound 1 9 carbons = nonane 2 4 3 5 6 7 8 9 Step #1: For a branched hydrocarbon, the longest continuous chain of carbon atoms gives the root name for the hydrocarbon

17 Nomenclature Practice
Name this compound 9 carbons = nonane 1 2 4 3 5 6 CH3 = methyl 7 chlorine = chloro 8 9 Step #2: When alkane groups appear as substituents, they are named by dropping the -ane and adding -yl.

18 Nomenclature Practice
Name this compound 9 carbons = nonane 1 2 4 3 5 6 CH3 = methyl 7 chlorine = chloro 8 9 1 9 NOT 9 1 Step #3: The positions of substituent groups are specified by numbering the longest chain of carbon atoms sequentially, starting at the end closest to the branching.

19 Nomenclature Practice
Name this compound 9 carbons = nonane 1 2 4 3 5 6 CH3 = methyl 7 chlorine = chloro 8 9 2-chloro-3,6-dimethylnonane Step #4: The location and name of each substituent are followed by the root alkane name. The substituents are listed in alphabetical order (irrespective of any prefix), and the prefixes di-, tri-, etc. are used to indicate multiple identical substituents.

20 Practice P. 11-16 #1, 2 Naming Alkanes Worksheet
Alkane Challenge Worksheet

21 Naming Alkenes & Alkynes
Count the number of C’s in the longest chain containing the double/triple bond. This is the parent chain, determine the root Number the parent chain so that the double/triple bond has the lowest possible position number Identify the position numbers of branches Same rules as before Write the branches in alphabetical order Write the root, including a prefix that identifies the position of the double/triple bond Add the prefix “cyclo” if its cyclic Add the suffix “ene” or “yne”

22 Naming Alkenes & Alkynes

23 Structural Isomers Structural isomers are compounds with the same molecular formula but different structural arrangements They will have different physical and chemical properties Example: pentane 2-methylbutane 2,2-dimathylpropane

24 Cis-Trans Isomers Cis-trans isomers occur when different groups of atoms are arranged around a double bond Unlike a single C-C bond that can rotate, the double C=C bond is fixed Opposite side Same side cis-1,2-dichloroethene trans-1,2-dichloroethene

25 Cis-Trans Isomers Examples: cis-3-pentene trans-2-hexene

26 Naming Aromatics Same rules
If benzene is the parent chain “benzene” suffix If benzene is a branch group “phenyl”

27 Practice P. 16-22 #3-7, 8abc Naming Alkenes/Alkynes Worksheet
Isomer Challenge Worksheet Naming Hydrocarbons Worksheet


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