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Organic Chemistry

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Organic Chemistry. Chemistry of Carbon Compounds. Why so many Carbon compounds?! Group #_ 14 __________________ metal, nonmetal, metalloid bond type__ covalent__ __ Valance electrons__4__ Lewis Dot formula Bonding Capacity__4____. C. C. C. C. C. C. C. Triple Bond. - PowerPoint PPT Presentation
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Organic Chemistry Chemistry of Carbon Compounds
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Page 1: Organic Chemistry

Organic Chemistry

Chemistry of Carbon Compounds

Page 2: Organic Chemistry

Why so many Carbon compounds?!

Group #_14__________________metal, nonmetal, metalloidbond type__covalent____Valance electrons__4__ Lewis Dot formulaBonding Capacity__4____

C

C C CC C C

Single Bond Double Bond Triple Bond

Page 3: Organic Chemistry

Bonding Capacity of H, O, N

O NH

1 2 3

Page 4: Organic Chemistry

Hmmm, I seem to remember something about that.......

Electronegativity:

METALS NONMETALS

Why covalent bonds?

·The ability to pull electrons away from another element

·elements in the NE part of the periodic table have stronger pull

Page 5: Organic Chemistry

Properties of Covalent Compounds

·Covalent compounds generally have much lower melting and boiling points than ionic compounds.

·Covalent compounds don't conduct electricity in water.

·Covalent compounds aren't usually very soluble in water.

·Covalent compounds tend to be more flammable than ionic compounds.

Page 6: Organic Chemistry

Chemical Formulas (Molecular formulas)

CH4 methane

C2H6 ethane

Structural Formulas

Lewis Dot

C

H

H

H

H C CH

H

H H

H

H

C

H

H

H

H C CH

H

H H

H

Heach pair of electrons = one single bond

one pair of electrons

Page 7: Organic Chemistry

Condensed Structural Formula

C3H8

C C C

H

H

H

H

H

H

H

H

CH3CH2CH3

Propane

Structural Formula

Chemical (molecular) Formula

Condensed Structural Formula

same as structural just take away the lines!

Page 8: Organic Chemistry

TRY IT

C4H10

Page 9: Organic Chemistry

ANOTHER WAY

C6H14

count how many CH2's there are

Page 10: Organic Chemistry

HOMOLOGOUS SERIES

·a series of organic compounds with a similar general formula·possessing similar chemical properties due to the presence of the same functional group, and ·shows a gradation in physical properties as a result of increase in molecular size and mass

Page 11: Organic Chemistry

ALKANES

·straight-chain or branched-chain hydrocarbons in which all the bonds between carbon atoms are single covalent bonds.

·"saturated"

·general formula is CnH2n+2 where "n" is the # of carbons

·end with the suffix " ane "

Page 12: Organic Chemistry

Naming Straight Chain Alkanes (CnH2n+2)

Prefix is determined by the number of carbon atoms in the chain: Suffix is "ane"

meth C1 CH4

eth C2 C2H6

prop C3but C4pent C5hex C6hept C7oct C8non C9dec C10

Page 13: Organic Chemistry

Functional Group

Functional groups are specific atoms, ions, or groups of atoms having consistent properties. A functional group makes up part of a larger molecule.

In branched alkanes the functional group in an "ALKYL" group

methylethyl

Naming Branched Alkanes

CH3

C2H5

one less Hydrogen!

yl ending

Page 14: Organic Chemistry
Page 15: Organic Chemistry
Page 16: Organic Chemistry

3,4-dimethyl heptane

Page 17: Organic Chemistry
Page 18: Organic Chemistry

· Name and number the longest carbon chain as for a straight chain alkane.· Identify each of the branches (side-chains).· Use the lowest number combinations for the branches (side-chains).

· Name each branch or side-chain (alkyl group) : methyl CH3 ethyl C2H5 propyl C3H7

· For more than 1 of the same alkyl group use: di = 2 tri = 3 tetra = 4

· Use commas between numbers, eg, 1,2 or 2,3· Use hyphens between numbers and words, eg, 2-methyl or 2,3-dimethyl· If there is more than 1 type of branch or side-chain, arrange their names alphabetically, ie, ethyl groups are named before methyl groups which are named before propyl groups

Naming Branched Chain Alkaneshttp://www.ausetute.com.au/nambanes.html

Page 19: Organic Chemistry

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