Open Question
Provide the structure of the urethane molecule created from the reaction between phenyl isocyanate and ethylene diol.
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- 1. A Review of General Chemistry5h 5m
- Summary23m
- Intro to Organic Chemistry5m
- Atomic Structure16m
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- 25. Condensation Chemistry2h 9m
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- 27. Heterocycles2h 0m
- Nomenclature of Heterocycles15m
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- Reactions of Pyrrole, Furan, and Thiophene13m
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- Peptides12m
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- Intro to Citric Acid Cycle7m
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- The Citric Acid Cycle35m
- 34. Nucleic Acids1h 32m
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- Electron Configuration of Elements45m
- Coordination Complexes20m
- Ligands24m
- Electron Counting10m
- The 18 and 16 Electron Rule13m
- Cross-Coupling General Reactions40m
- Heck Reaction40m
- Stille Reaction13m
- Suzuki Reaction25m
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- Kumada Coupling Reaction13m
- Negishi Coupling Reaction16m
- Buchwald-Hartwig Amination Reaction19m
- Eglinton Reaction17m
- Catalytic Allylic Alkylation18m
- Alkene Metathesis23m
- 36. Synthetic Polymers1h 49m
- Introduction to Polymers6m
- Chain-Growth Polymers10m
- Radical Polymerization15m
- Cationic Polymerization8m
- Anionic Polymerization8m
- Polymer Stereochemistry3m
- Ziegler-Natta Polymerization4m
- Copolymers6m
- Step-Growth Polymers11m
- Step-Growth Polymers: Urethane6m
- Step-Growth Polymers: Polyurethane Mechanism10m
- Step-Growth Polymers: Epoxy Resin8m
- Polymers Structure and Properties8m
36. Synthetic Polymers
Step-Growth Polymers: Urethane
Multiple Choice
Name the alcohol that was used to create the following urethane molecule.
A
(1S,3S)-3-methyl-1-cyclopentanol
B
(1S,3R)-3-methyl-1-cyclopentanol
C
(1R,3S)-3-methyl-1-cyclopentanol
D
(1R,3R)-3-methyl-1-cyclopentanol
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Master Step-Growth Polymers: Urethane Concept 1 with a bite sized video explanation from Jules Bruno
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