Chapter 25 Organic and Biological Chemistry
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Transcript of Chapter 25 Organic and Biological Chemistry
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Chapter 25Organic and Biological
Chemistry
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Organic Chemistry• The chemistry of carbon
compounds.• Carbon has the ability to form long
chains.• Without this property, large
biomolecules such as proteins, lipids, carbohydrates, and nucleic acids could not form.
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Hydrocarbons
• Four basic types:AlkanesAlkenesAlkynesAromatic hydrocarbons
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Alkanes
• Only single bonds.• Saturated hydrocarbons.
“Saturated” with hydrogens.
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Formulas
• Lewis structures of alkanes look like this.• Also called structural formulas.• Often not convenient, though…
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Formulas
…so more often condensed formulas are used.
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Properties of Alkanes
• Only van der Waals force: London force.• Boiling point increases with length of chain.
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Isomers
Have same molecular formulas, but atoms are bonded in different order.
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Organic Nomenclature
• Three parts to a compound name:Base: Tells how many carbons are in the longest
continuous chain.
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Organic Nomenclature
• Three parts to a compound name:Base: Tells how many carbons are in the longest
continuous chain.Suffix: Tells what type of compound it is.
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Organic Nomenclature
• Three parts to a compound name:Base: Tells how many carbons are in the longest
continuous chain.Suffix: Tells what type of compound it is.Prefix: Tells what groups are attached to chain.
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To Name a Compound…
1. Find the longest chain in the molecule.
2. Number the chain from the end nearest the first substituent encountered.
3. List the substituents as a prefix along with the number(s) of the carbon(s) to which they are attached.
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To Name a Compound…
If there is more than one type of substituent in the molecule, list them alphabetically.
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Cycloalkanes• Carbon can also form ringed structures.• Five- and six-membered rings are most stable.
Can take on conformation in which angles are very close to tetrahedral angle.
Smaller rings are quite strained.
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Alkenes
• Contain at least one carbon–carbon double bond.• Unsaturated.
Have fewer than maximum number of hydrogens.
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Structure of Alkenes
This creates geometric isomers, which differ from each other in the spatial arrangement of groups about the double bond.
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Nomenclature of Alkenes• Chain numbered so double bond gets smallest
possible number.• cis- alkenes have carbons in chain on same side of
molecule.• trans- alkenes have carbons in chain on opposite
side of molecule.
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Alkynes
• Contain at least one carbon–carbon triple bond.• Carbons in triple bond sp-hybridized and have
linear geometry.• Also unsaturated.
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Nomenclature of Alkynes
• Analogous to naming of alkenes.• Suffix is -yne rather than –ene.
4-methyl-2-pentyne
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Aromatic Hydrocarbons
• Cyclic hydrocarbons.• Molecule is planar.• Many aromatic
hydrocarbons are known by their common names.
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Structure of Aromatic Compounds
• Two substituents on a benzene ring could have three possible relationshipsortho-: On adjacent carbons.meta-: One carbon between them.para-: On opposite sides of ring.
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Functional Groups
Term used to refer to parts of organic molecules where reactions tend to occur.
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Alcohols• Contain one or more hydroxyl groups, —OH
• Named from parent hydrocarbon; suffix changed to -ol and number designates carbon to which hydroxyl is attached.
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Ethers
• Tend to be quite unreactive.• Therefore, they are good polar solvents.
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Carbonyl Compounds
• Contain C—O double bond.
• Include many classes of compounds.
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Aldehydes
At least one hydrogen attached to carbonyl carbon.
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Ketones
Two carbons bonded to carbonyl carbon.
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Carboxylic Acids
• Have hydroxyl group bonded to carbonyl group.
• Tart tasting.• Carboxylic acids are
weak acids.• Naming:
_____oic acid
CH3COOH
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Carboxylic Acids
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Esters• Products of reaction
between carboxylic acids and alcohols.
• Found in many fruits and perfumes.
butanoate
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Amines
• Organic bases.• Generally have strong, unpleasant odors.
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Amides
Formed by reaction of carboxylic acids with amines.
This is the reaction that occurs between amino acids
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Amino Acids and Proteins
• A condensation reaction between the amine end of one amino acid and the acid end of another produces a peptide bond.