Title: Alcohols
1Alcohols
- Nomenclature
- Properties
- Preparation
- Reactions
- Spectroscopy
2Alcohol Nomenclature
3Preparation Reactions
- Reduction of carbonyl compounds
- Hydration of Alkenes
- Grignard reactions
4Reduction of Carbonyl Compounds
- Reduction of Aldehydes/ketones
- Reduction of Carboxylic acids/Esters
5Reduction of Aldehydes/Ketones
6Reduction of Aldehydes/Ketones
7Reduction of Carboxylic Acids and Esters
- Lithium Aluminum Hydride Reduction
8Hydration of Alkenes
- Acid catalyzed Hydration
- Oxymercuration-Demercuration
- Hydroboration-Oxidation
9Acid-Catalyzed Hydration of Alkenes
- Markovnikov addition
- Formation of most stable carbocation
- Shifts/rearrangements possible
10Hydration of Alkenes via Oxymercuration/Demercurat
ion
- Markovnikov addition
- Typically no shifts/rearrangements
- Mercurinium ion involvement
11Hydroboration-Oxidation of Alkenes
- Anti-Markovnikov addition
- No shifts/rearrangements
- Syn addition
12Grignard Addition Reactions
- Addition to Aldehydes/Ketones
- Addition to Esters
- Addition to Epoxides
13Grignard Additions to Aldehydes/Ketones
- Formation of primary, secondary, and tertiary
alcohols
14Grignard Additions to Esters
- Formation of secondary and tertiary alcohols
15Grignard Addition to Epoxides
16Typical Alcohol Reactions
- Salt formation
- Dehydration
- Oxidation
- Alkyl halide formation
- Ester formation
- Ether synthesis
- Periodic acid cleavage of glycols
- Haloform reaction of methyl carbinols
- THP acetal formation
17Conversion of Alcohols to Salts
- Reaction with Active Metals
18Dehydration of Alcohols
19Oxidation of Alcohols
20Alcohol Conversion to Alkyl Halides
- Reaction with Hydrogen halides
- Reaction with Thionyl chloride
- Reaction with Phosphorus trihalides or
pentahalides
21Hydrogen Halide Conversion of Alcohols to Alkyl
Halides
22Conversion of Alcohols to Alkyl Chlorides via
Thionyl Chloride
23Conversion of Alcohols to Alkyl Halides via
Phosphorus Halides
24Ester Formation from Alcohols
25Periodic Acid Cleavage of Glycols
26Haloform Reaction
- Methyl carbinol cleavage to give Carboxylic acids
and Haloform
27Disguising an Alcohol
- Creating a tetrahydropyranyl acetal
28Spectroscopic Characteristics of Alcohols
29Ethers
- Nomenclature
- Properties
- Preparation
- Reactions
30Ether Nomenclature
31Preparation of Ethers
- Dehydration of Alcohols
- Williamson synthesis
- Alkoxymercuration- Demercuration
- Peroxyacid Epoxidation of Alkenes
32Ether Formation via Acid Catalyzed Dehydration of
Alcohols
33Williamson Synthesis of Ethers
- Bimolecular Substitution by Alkoxide on a
suitable substrate
34Alkoxymercuration-Demercuration of Alkenes
- Markovnikov Addition
- Typically no rearrangements/shifts
- Mercurinium ion involvement
35Epoxidation of Alkenes
36Ether Reactions
- HX Cleavage
- Epoxide Ring Opening
37HX Cleavage of Ethers
- Unimolecular or Bimolecular Cleavage Pathways
38Epoxide Ring Opening
- Unimolecular or Bimolecular