@since carbon atoms have 4 valence shell electrons they can easily form bonds at four locations with...

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Since carbon atoms have 4 valence shell electrons they can easily form bonds at four locations with other atoms of carbon, hydrogen, oxygen, and halogens. One of the more common families of compounds have carbon atoms bonded to each other, end to end, with H atoms bonded at the remaining locations. These compounds of carbon and

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Since carbon atoms have 4 valence shell electrons they can easily form bonds at four locations with other atoms of carbon, hydrogen, oxygen, and halogens.

One of the more common families of compounds have carbon atoms bonded to each other, end to end, with H atoms bonded at the remaining locations.

These compounds of carbon and hydrogen are known as hydrocarbons.

When no double or triple bonds between adjacent carbon atoms exist the compounds have a maximum number of hydrogen atoms on the carbon chain and are called saturated hydrocarbons.This family of hydrocarbons are called theALKANES and are named for the number of carbon atoms in the chain. The basic formula is CnH2n+2. Here is an example

C C C C C C C C C C C CHH H

H H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

HH

H

H

For simplicity the pairs of electrons are usually represented by sticks which represent covalent bonds

H

H H

H H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

C C C C C C C C C C C C

Saturated hydrocarbons are named Alkanes with the number of carbons in the chain determining the beginning of the name, while the end of the name is

_______ane

1 carbon methane CH4 H

H

H

HC

H

H

H

C HC

H

H

HC

H

H

H

H

H

C C

H

H

2 carbons ethane C2H6

3 carbons propane C3H8

4 carbons butane C4H10

5 carbons pentane C5H12

C

H

H

H

H

H

C C

H

H

HC

H

H

C

H

H

H

H

H

C C

H

H

C

H

H

HC

H

H

6 carbons hexane C6H14

C

H

H

H

H

H

C C

H

H

C

H

H

C

H

H

C

H

H

H

7 carbons heptane C7H16

C

H

H

H

H

H

C C

H

H

C

H

H

C

H

H

C

H

H

HC

H

H

8 carbons octane C8H18

C

H

H

H

H

H

C C

H

H

C

H

H

C

H

H

C

H

H

HC

H

H

C

H

H

9 carbons nonane C9H20

C

H

H

H

H

H

C C

H

H

C

H

H

C

H

H

C

H

H

HC

H

H

C

H

H

C

H

H

10 carbons decane C10H22

C

H

H

H

H

H

C C

H

H

C

H

H

C

H

H

C

H

H

HC

H

H

C

H

H

C

H

H

C

H

H

Since hydrogen atoms are assumed to fill all spot around the C atoms they are sometimes left out. These are called carbon skeleton diagrams. An example of a carbon skeleton diagram for hexane could be:

C - C - C - C - C - C or

C - C - C | C - C | C

It is important to note that chains of C atoms do not have to be drawn horizontally. As long as they are drawn in a continuous string each C atom can be bonded to an adjacent C atom in any of the 3 remaining places

If this is the beginning of an 8 carbon chain

- CC

The next carbon atom can go here

Or here

Or here

C |

|C

C -

Or here

This can lead to a multitude of possible 2 dimensional drawings for the same molecule.Here are just a few of the possibilities for octane

C - C | C - C |C - C - C - C

C - C - C | C - C | C - C | C

C | C - C - C |C - C - C - C

C - C | C - C | C - C | C - C

Remember each C atom has 2 H atoms bonded to it,with an additional H atom bonded to the C atom at each end of the chain

Some hydrocarbons have adjacent carbon atoms with double bonds. This reduces the number of hydrogen atoms bonded to the carbon chain by 2 hydrogens. These hydrocarbons are named Alkenes with the number of carbons in the chain determining the beginning of the name, while the end of the name is _______ene

C C C C C C C C C C C CHH H

H H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

H

HH

H

H

C C C C C C C C C C C CHH H

H H

H

H

H

H

H

H

H H H

H

H

H

H

H

H

HH

H

H

Notice when adjacent carbon atoms use 2 additional electrons to form the 2nd bond there are 2 fewer places for H atoms to bond. This reduces the number of H atoms by 2 creating the general formula CnH2n

2 carbons ethene C2H4 H

H

C HC

H

3 carbons propene C3H6H

C H

H

H

H

C C

H

H

C

H

H

H

C C

H H

C H

H

4 carbons butene C4H8

H

C

H

H

H

C C

H H

C H

H

Notice when the carbon chain reaches a length of 4 carbons, the double bond can be placed between the end carbons or the middle carbons. Each of these structures is a different hydrocarbon. The top one is called 1-butene and the bottom one is called 2-butene. This naming method numbers the carbon skeleton chain in a way which encounters the double bond with the lowest possible number.

1 2 3 4

H

CH

H

C C

H H

C H

H1 2 3 4H

Isomers are compounds with the same formula but different structures.C5H10 is calledpentene.How many different pentenes are there?

H

C

H

H

H

C C

H H

C

H

H

C H

HH

CH

H

C C

H H

C

H

H

C H

HH

H

CH

H

C C

H H

CH

H

C H

HH

1-pentene

2-pentene

3-pentene is the same as 2-pentene

Draw all possible hexenes, heptenes, octenes, nonenes and decenes. 1-hexene

2-hexene3 hexene1-heptene2-heptene3-heptene1-octene2-octene3-octene4-octene1-nonene2-nonene3-nonene4-nonene1-decene2-decene3-decene, 4-decene, 5-decene

CH2

CH

CH2

CH2

CH2

CH3

CH3

CH

CH

CH2

CH2

CH3

CH3

CH2

CH

CH

CH2

CH3

1-hexene

2-hexene

3-hexene

CH2

CH

CH2

CH2

CH2

CH2

CH3

CH3

CH

CH

CH2

CH2

CH2

CH3

CH3

CH2

CH

CH

CH2

CH2

CH3

1-heptene

2-heptene

3-heptene

Isomers

CH2

CH

CH2

CH2

CH2

CH2

CH2

CH3

CH3

CH

CH

CH2

CH2

CH2

CH2

CH3

CH3

CH2

CH

CH

CH2

CH2

CH2

CH3

CH3

CH2

CH2

CH

CH

CH2

CH2

CH3

1-octene

2-octene

3-octene

4-octene

Isomers

CH2

CH

CH2

CH2

CH2

CH2

CH2

CH2

CH3

CH3

CH

CH

CH2

CH2

CH2

CH2

CH2

CH3

CH3

CH2

CH

CH

CH2

CH2

CH2

CH2

CH3

CH3

CH2

CH2

CH

CH

CH2

CH2

CH2

CH3

1-nonene

2-nonene

3-nonene

4-nonene

Isomers

CH2

CH

CH2

CH2

CH2

CH2

CH2

CH2

CH3

CH3

CH

CH

CH2

CH2

CH2

CH2

CH2

CH3

CH3

CH2

CH

CH

CH2

CH2

CH2

CH2

CH3

CH3

CH2

CH2

CH

CH

CH2

CH2

CH2

CH3

CH3

CH2

CH2

CH2

CH

CH

CH2

CH2

CH2

CH3

1-decene

2-decene

3-decene

4-decene

5-decene

Isomers

Alkenes can have multiple double bonds. If they have 2 double bonds they are called dienes, 3 double bonds - trienes, 4 double bonds tetraenes, etc.Draw a diagram for propadiene. C H

HCC

HH

What is the name of this

CCCCC C C C

Is it 3,4,7 -octatriene or 1,4,5 - octatrieneWhich starts with the lowest numbers?

Some hydrocarbons have adjacent carbon atoms with triple bonds. This reduces the number of hydrogen atoms bonded to the carbon chain by 4 hydrogens. These hydrocarbons are named Alkynes with the number of carbons in the chain determining the beginning of the name, while the end of the name is _______yne

Draw a diagram for 2-pentyne.

CH

H

C CH

CH

C H

HH HRemember the carbon chain can be numbered from left to right or right to left as long as the lowest possible numbered carbon begins the triple bond.In general what would be the formula for alkynes?CnH2n-2

CH3

CH2

C

C

C

CHWhat is the name of this structure?

1,3-hexadiyne6 carbonsLocation of triple bonds2 triple bondsalkyne

Draw a structural diagram, showing all atoms, for 2,4,6-nonatriyne.

CH3

CH2

C

C

C

C

C

C

CH3

Carbon chains can also be bent back on themselves to form a closed chain. When this happens 2 hydrogen atoms are lost.

C

C

C CC

CC

H

H

H

H

H

HH

H

H

H

HH

H

H HHIf these 2

carbons bond together 2 hydrogen atoms must be removed

Name?cycloheptane

Construct the diagram for 1,3,5 - cyclohexatriene

C C C C C C

H

HH

H

HH

Or

This structure is so common, it is given its own name, Benzene, and is usually drawn this way since further analysis has revealed the bonds between C atoms are neither single or double bonds but something in between. It is believed all the carbon atoms and hydrogen atoms in this ring share the electrons equally

Benzene as a side chain is namedphenyl

CH2

CH

CH2

CH

CH2

Name this structure.cyclopentene

CH2

CH

CH2

CH2

CH

CH

CH2

CH

Name is 1,4-cyclooctadiene

CH2

CH2

C

C

C

CH2

CDraw structural diagram showing all H atoms for 1,4-cycloheptadiyne

C

C

C

C

C

C

Name1,3,5-cyclohexatriyne