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3.1-3.2 INTRODUCTION TO ORGANIC COMPOUNDS

3.1-3.2 INTRODUCTION TO ORGANIC COMPOUNDS

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3.1-3.2 INTRODUCTION TO ORGANIC COMPOUNDS. Organic Chem and Macromolecules. Organic Chem and Functional Groups. Got Phenylalaninedehydroxylase ?. Phenylaline is a toxic amino acid. Phenylalaninedehydroxylase breaks it down . 0. Space-filling model. Structural formula. - PowerPoint PPT Presentation

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Page 1: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

3.1-3.2INTRODUCTION TO ORGANIC COMPOUNDS

Page 2: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Organic Chem and Macromolecules

Page 3: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Organic Chem and Functional Groups

Page 4: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Got Phenylalaninedehydroxylase?

Page 5: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Phenylaline is a toxic amino acid

Page 6: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Phenylalaninedehydroxylase breaks it down

Page 7: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

•Life’s molecular diversity is based on the properties of carbon– A carbon atom can form four covalent bonds

• Allowing it to build large and diverse organic compounds

Structuralformula

Methane

H H

H

H H H

H

H

Ball-and-stickmodel

Space-fillingmodel

CC

The 4 single bonds of carbon point to the corners of a tetrahedron.

Figure 3.1A

Page 8: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Fig. 4-3

NameMolecular Formula

Structural Formula

Ball-and-StickModel

Space-FillingModel

(a) Methane

(b) Ethane

(c) Ethene (ethylene)

Page 9: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Carbon Configuration

• Chain

• Branched chain

• Ring Structure

Page 10: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Carbon skeletons vary in length.PropaneEthane

Length.

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Skeletons may be unbranched or branched.

Butane Isobutane

Branching.

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Double bonds.

2-Butene

Skeletons may have double bonds,which can vary in location.

1-Butene

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Cyclohexane Benzene

Skeletons may be arranged in rings.Rings.

Page 14: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Isomers

• Isomers – same chemical formula, but different chemical arrangement

• 3 different types of isomers

Page 15: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Structural isomer-differ in arrangement of covalent bonds

Page 16: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Geometric isomer-differ in spatial arrangement

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Enantiomer isomer- “mirror image”

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4 macromolecules

• Carbohydrates

• Lipids

• Proteins

• Nucleic Acids

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Functional Groups!

• These are like name tags for large macromolecule groups

Glucose

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Hydroxyl

• Hydroxyl –OH (sometimes referred to as alcohol.)

• Found in alcohol compounds

• Example: Ethanol

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Carbonyl

• Keto =CO

• Aldehyde -CHO

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Carboxyl

• Carboxyl -COOH found in acids

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Amino

• Amino -NH2 found in amino acids

phenylalanine

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Methyl

• Methyl –CH3

Page 25: 3.1-3.2 INTRODUCTION  TO ORGANIC COMPOUNDS

Phosphate

• Phosphate - PO4

• Unstable due to electronegativity

• Found in ATP, DNA, RNA

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Functional Groups make recognizing macromolecules easier

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