Organic Chemistry- Rotating Rainbows
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 the 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 Demonstration II – Molecular Vibrations
IR Demonstrations 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
Electrophilic Aromatic Substitution Reaction/EAS Reaction
Reactivity of Alkanes vs. Aromatic Compounds
Inductive Effect
Optical Activity of Racemic Mixtures With Limonene
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
Terephthalate Monomerization
Rotating Rainbows
Description: Karo syrup and water are placed on the overhead projector between crossed polarizers. As the upper polarizer is rotated over the Karo syrup and the lower polarizer, the relative angle between the plane polarizer orientation changes, thereby allowing specific wavelength ranges of color to pass through the polarizers from the white light emitted by the overhead projector lamp. This effect is seen when the liquid placed in the beaker between the polarizers has a structure which rotates polarized light. This kind of molecule is called optically active. Water is not an optically active molecule so changing the relative angle between the polarizer planes does not affect the properties of the light that passes through it.
Source: Journal of Chemical Education
Year: 1999 Vol: 76 Page: 1233 – 1236
Keywords: Isomers, Stereoisomers
Rating: - Electric shock hazard
- Breakage hazard
- Results are clearly observable without guidance
- Good connection from demo to course material
- Low failure rate
- Time to results is low
- Good effects are seen by audience
- Simple procedures
- Simple manipulations for most to perform
- Use of glass surfaces, handle with care
- Eye protection required
- Use of UL approved three-prong plug and outlet required
Class: Organic Chemistry, Molecular Structure
Division: General, Organic Chemistry
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