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organic chem

Science 30 – Organic Chemistry Study Guide

PART A: Functional Groups and Structures

Know how to:

  • Identify functional groups

  • Name compounds (IUPAC)

  • Draw condensed and structural formulas

Functional Groups to Know:

Functional Group

Description

Example

Alcohol (-OH)

Hydroxyl attached to a carbon

Butan-2-ol

Carboxylic Acid (-COOH)

Carbon double bonded to O and single bonded to OH

Pentanoic acid

Ester (-COO-)

Formed from acid + alcohol

Ethyl butanoate

Halogenated Hydrocarbon

Hydrocarbon with Cl, Br, F, or I

1,1,2,2-tetrachloroethane

Examples from the Sheet:

  • Pentanoic acid = carboxylic acid

  • Butan-2-ol = alcohol

  • Ethyl butanoate = ester

  • 2-bromo-2-chloropentane = halogenated hydrocarbon


PART B: Organic Reactions

1. Esterification

Alcohol + Carboxylic Acid → Ester + Water

Examples:

  • Ethanoic acid + Butan-1-ol → Butyl ethanoate + H₂O

  • Propanoic acid + Pentan-1-ol → Pentyl propanoate + H₂O

Important:

  • Use H₂SO₄ as a catalyst

  • Draw out full Lewis/structural diagrams when asked


PART C: Identifying Functional Groups in Molecules

Look for:

  • Carboxylic Acid: -COOH

  • Alcohol: -OH on a carbon

  • Halides: Cl, Br, F, I on a carbon

  • Benzene ring: hexagon with circle or alternating double bonds

  • Esters: R-COO-R'

  • Ethers, Aldehydes (less focus but sometimes shown)

Basics of Organic Chemistry

Organic Chemistry is the study of carbon-based compounds.

Key Characteristics:

  • Carbon can form 4 covalent bonds

  • Forms chains, branched chains, and rings

  • Bonds with hydrogen, oxygen, nitrogen, halogens, sulfur

Hydrocarbons: compounds made only of carbon and hydrogen
Types:

  • Alkanes: only single bonds (saturated)

  • Alkenes: at least one double bond (unsaturated)

  • Alkynes: at least one triple bond (unsaturated)

  • Aromatic compounds: contain a benzene ring


2. Naming Hydrocarbons (IUPAC Rules)

Steps:

  1. Identify the longest carbon chain (parent chain)

  2. Number the chain to give the lowest number to the first branch or double/triple bond

  3. Name the branches (alkyl groups) and assign numbers

  4. Use prefixes: di-, tri-, tetra- for multiple groups

  5. Combine name: #-branch-parent chain

Examples:

  • CH₄ = Methane

  • C₂H₆ = Ethane

  • CH₃CH₂CH₃ = Propane

  • CH₃CH=CH₂ = Propene

Prefixes (1-10 carbon atoms):
meth-, eth-, prop-, but-, pent-, hex-, hept-, oct-, non-, dec-


3. Functional Groups and Derivatives

Functional Group

Type of Compound

Ending

Example

-OH

Alcohol

-ol

Ethanol

-COOH

Carboxylic acid

-oic acid

Ethanoic acid

-COO-

Ester

-oate

Methyl propanoate

-Cl, -Br, -I

Halides

halo-

Chloromethane

-NH₂

Amine

-amine

Ethanamine

-CHO

Aldehyde

-al

Ethanal

-C=O (middle)

Ketone

-one

Propanone


4. Drawing Structural Formulas

  • Condensed: CH₃CH₂CH₃

  • Expanded/Structural: show each bond

  • Line Diagrams: each line represents a bond, ends/junctions are carbon atoms


5. Types of Organic Reactions

Type

Description

Example

Combustion

Reaction with O₂ to form CO₂ + H₂O

CH₄ + 2O₂ → CO₂ + 2H₂O

Substitution

One atom replaces another

CH₄ + Cl₂ → CH₃Cl + HCl

Addition

Double/triple bonds become single

CH₂=CH₂ + H₂ → CH₃CH₃

Elimination

Opposite of addition (forms double bonds)

CH₃CH₂OH → CH₂=CH₂ + H₂O

Esterification

Alcohol + acid → ester + water

CH₃OH + CH₃COOH → CH₃COOCH₃ + H₂O