1. Alcohols Oh yeah!

2. Alcohol Compound where a hydroxyl group (-OH) replaces one of the hydrogens on a carbon General Formula: – R- OH Example: – CH 3 CH 2 CH 2 OH – 1-propanol

3. Alcohol Nomenclature Alcohols end with the suffix “-ol” Like alkenes and alkynes, the longest continuous chain must contain the hydroxyl group (-OH). – Also, count the carbons so that the hydroxyl group has the lowest number possible Unlike alkenes/alkynes, the location of the hydroxyl group interrupts the base name and the number goes directly before the –ol Branches are names as usual Example: 3-methylbutan-1-ol

4. Types of Alcohols Each alcohol is defined by having a C-OH bond. So there are three other bonds on that carbon… to determine what type of alcohol it is, simple count the things bonded to the carbon that aren’t hydrogens. (often labeled as “R” groups) 3 Types – Primary Alcohol Alcohol with only 1 “R” group…. – Secondary Alcohol Alcohol with 2 “R” groups… – Tertiary Alcohol Alcohol with 3“R” groups…

5. Properties of Alcohols Hydroxyl group is polar and allows for hydrogen bonding to water molecules – Alcohols have high melting and boiling points than corresponding alkanes – Alcohols with fewer than 7 carbons are liquids are room temp Methanol and ethanol are colourless, have low boiling points, and are liquids with slightly sharp, sweet smells – Alcohols with less than 5 carbons dissolve both in water and in non- polar organic liquids Longer carbon chain alcohols become progressively less soluble in water

6. ***Reactions of Alkenes and Alkynes Oxidation – Alkenes undergo an oxidation reaction with acidified potassium permanganate, KMnO 4 /H + (not simply KMnO 4 ) Forms a “diol”

7. Reactions of Alcohols Oxidation Reactions Alcohols can undergo oxidation reactions with acidified potassium permanganate, KMnO 4 /H + or acidified potassium dichromate K 2 Cr 2 O 7 /H + – Oxidation of Primary Alcohols Symbol [O] above a rxn arrow indicates an oxidation rxn. 1 st product of an oxidation of primary alcohol is and aldehyde. Aldehydes can then be oxidized into carboxylic acids

8. Reaction of Alcohols Test for Primary Alcohol – Tollen’s Test: Reduces Ag + to solid Ag – seen as a black suspension or ‘silver mirror’ – happens with Aldehydes (the 1 st product of oxidation of primary alcohols). Secondary alcohols don’t create aldehydes – they create ketones. Ergo, Tollen’s test can be used to tell the difference b/w aldehydes and ketones

9. Reaction of Alcohols Test for Primary Alcohol – Fehling’s or Benedict’s Reagents: Uses copper compounds to test for aldehyde Cu 2+ (blue) is reduced by aldehydes to Cu + (red suspension)

10. Reaction of Alcohols Reflux Equipment is used to completely oxidize primary alcohols to carboxylic acids (returns vaporized aldehydes to mixture to finish oxidizing)

11. Reaction of Alcohols Oxidation Reactions – Oxidation of Secondary Alcohols Oxidised to a ketone (RCOR’) – Oxidation of Tertiary Alcohols – Can’t happen

12. Reaction of Alcohols Substitution with Thionyl Chloride (SOCl 2 ) – Alcohols react with chlorinating agents to give a choloralkane

13. Reaction of Alcohols Condensation reaction (Esterification) – Alcohol + Carboxylic Acid  ester (RCOOR’) Often have sweet, fruity smell – Usually done with dehydrating agent (concentrated sulfuric acid) – Uses reflux equipment – no loss to evaporation

14. Reaction of Alcohols Elimination Reaction of Alcohols Reverse of Markovnikov’s Rule: H is eliminated from the carbon atom which has the lowest number of H atoms