Organic Chemistry- Reactivity of Alkanes vs. Aromatic Compounds

Bromination of Saturated and Unsaturated Hydrocarbons

Blue Bottle

Dehydration of Sugar by Sulfuric Acid

Disappearing Coffee Cup

Formation of a Silver Mirror

Models 360

Nylon 6 – 10

Organic Synthesis With Familiar Materials

Oxidation of Primary, Secondary, Tertiary Alcohols

Oxidation of Luminol

Polyurethane Foam

Slime

Underwater Fireworks: Chlorination of Acetylene

Carbide Lamp

Differences in Miscibility of Organic Alcohols With Increasing Chain Length

Combustion of Cellulose Nitrate (Guncotton)

Different Smells of Carvone Isomers

Distinguishing Between HD and LD Polyethylene

Enviro-bond: Cleaning Oil Spills

Esterification Using a Dean-Stark Trap

Ethanol Cannon

Happy/Sad Balls

IR Demonstration I – Atomic Coupling

IR Demonstrations II – Molecular Vibrations

IR Demonstration III – Molecular Vibrations

Making a Rubber Ball from Latex

Plastic Samples

Reaction Intermediates in Organic Chemistry

Reducing Sugars and Fehling’s Solution

Rod Climbing by a Polymer Solution

Rotating Rainbows

Silly Putty

Soap Emulsifies Hydrocarbons

Superabsorbent Polyacrylate Gel

Tubeless Siphon

Alkimers

Aniline Hydrochloride-Formaldehyde Polymer

Phenol-Formaldehyde Polymer

Saponification

Relative Reactivity of Reducing Agents

Inductive Effect

Optical Activity of Racemic Mixtures With Limonene

Electrophilic Aromatic Substitution Reaction/EAS Reaction

Reactivity of Alkanes vs. Aromatic Compounds

Relationship of Absorbed Light to Observed Color

Density and Miscibility of Liquids

Extraction of Copper Ions from Solution with Orform®

Gel Formation with Sodium Alginate and Calcium Chloride

Ozonolysis

Hydrolysis of T-Butyl Chloride: A Lecture and Lab Experiment

Reactivity of Alkanes vs. Aromatic Compounds

Description: A mixture of bromine in carbon tetrachloride is added to ungraduated cylinders, one containing pentane(l) and one containing benzene(l). Both cylinders change to a red-orange color upon mixing. High intensity light is directed through the mixture in each cylinder. After several seconds, one of the solutions is made clear and colorless as a result of the light after undergoing a photolytic substitution reaction. The other solution remains unchanged.

Source: UW Card Catalog

Year:  1992    Vol: N/A  Page: N/A

Keywords: Substitution Reaction, Bromine, Aromaticity, Photolysis

Rating:

Hazard: High

  • Flammable liquids
  • Acute toxicity hazard
  • Carcinogenicity hazard
  • Specific organ toxicity- Central Nervous System
  • Inhalation hazard
  • Skin corrosion hazard
  • Aspiration hazard
  • Aquatic toxicity hazard
  • Germ cell mutagenicity hazard

Effectiveness: Good

  • Results are observable without guidance
  • Good connection from demo to course material
  • Time to results is very low
  • Reliability is high
  • Counterintuitive effects are observed

Difficulty: Medium

  • Some careful manipulations required
  • Use of toxic reagents

Safety Precautions:

  • Eye protection and gloves required
  • Downdraft hood or fume hood required
  • ABC fire extinguisher on hand
  • Spill kit on hand
  • Avoid exposure to vapors, mists, gases, or droplets
  • Prevent release of reagents to the environment
  • 10% sodium thiosulfate solution on hand

Class: Types of Organic Reactions, Photolytic Substitution

Division: Organic Chemistry, General Chemistry