Reading...
Play button
Play button
Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
23 Cards in this Set
- Front
- Back
|
Mechanism of Grignard Reagents
|
Mechanism of Addition of Grignard to CO2
|
|
|
Mechanism of forming Gilman Reagents
|
Mechanism of Epoxide Breaking
|
|
|
Mechanism of Acetal Formation
|
Mechanism of Imine Formation
|
|
|
Mechanism of Enamine Formation
|
Mechanism of Wittig Reaction (Ylides)
|
|
|
Mechanism of Wolff-Kisner Reaction
|
Mechanism of Baeyer-Villiger Reaction
|
|
|
PCC Reaction - how primary and secondary alcohols will react
|
Jones Reagent - how primary & secondary alcohols will react
|
|
|
Formation of COOH (via Grignard)
|
Acetal Formation
|
|
|
Acetal Hydrolysis
|
Wittig Reaction
|
|
|
Imine Formation
|
Enamine Formation
|
|
|
Xi-Cleft of SJ
|
Huizong SJ 7
|
|
|
Epoxidation of Alkenes
|
Epoxidation of Vicinal Halohydrins
|
|
|
Formation of Vicinal Halohydrin
|
Acid Catalyzed cleavage of Ethers
|
|
|
Preparation of ethers from alcohols
|
Williamson Ether synthesis
|
|
|
Preparation of vicnal diols (hydroxylation)
|
Ways to form an alcohol
|
|
|
Mechanism - Protection of a C=O group
|
Hydration of acetone/ketone
|
|
|
Reduction of COOH/Ester to form OH
|
Reduce C=O to form OH on metal plate
|
|
|
Reduce C=O to form OH in basic solution (2 ways)
|
Which is stronger - LiAlH4 or NaBH4?
|
|
|
Organocopper synthesis of alkanes
|
Organolithium synthesis of alcohols
|
|
|
Organocopper Reagents and acid halides
|
Congugated nucleophilic addition
|
|
|
Grignard Reaction
|
Baeyer- Villiger Reaction
|
|
|
Conversion of Esters to aldehydes
|
Wolff-Kishner Reduction
|
|
|
Friedel-Crafts Alkylation
|
Friedel-Crafts Acylation
|
|
|
Hydroboration of Alkenes
|
Oxymercuration (formation of alcohol)
|
