Alcohols (CnH2n+2O_CnH2n+1OH) Flashcards
Name all 8 methods of alcohol production.
1.Hydration of alkenes.
2.Oxidation of alkenes with cold dilute acidified KMnO4(VII).
3.Nucleophilic substitution of Halogenoalkanes with aqueous OH- ion.
4.Nucleophilic substitution of Halogenoalkanes with water (hydrolysis).
5.Reduction of aldehydes.
6.Reduction of ketones.
7.Reduction of carboxylic acids.
8.Hydrolysis of esters.
Name all 5 reactions of alcohols.
1.Oxidation.
2.Dehydration.
3.Nucleophilic substitutions to form halogenoalkanes.
4.Esterification.
5.Alcohol+Metal—>MetalAlkoxide+H2.
Hydration of alkenes. EXAMPLE AND CONDITIONS.
Ethene+Steam—>Ethanol.
Conditions= 330°C/60ATM and concentrated H3PO4 catalyst.
Oxidation of alkenes with cold dilute acidified KMnO4(VII). EXAMPLE AND CONDITIONS.
Ethene+[O]—>Ethane-1,2-diol.
Conditions= Cold dilute H+/KMnO4(VII).
Nucleophilic substitution of Halogenoalkanes with aqueous OH- ion. EXAMPLE AND CONDITIONS.
Chloroethane+NaOH(aq)—>Ethanol+NaClO.
Conditions= Heat.
Nucleophilic substitution of Halogenoalkanes with water (hydrolysis). EXAMPLE AND CONDITIONS.
Chloroethane+H2O—>Ethanol+HCL.
Conditions= Heat and reflux with drops of acid or alkali.
Reduction of aldehydes to primary alcohols. EXAMPLE AND CONDITIONS.
Propanal+2[H]—>Propanol.
Conditions= NaBH4(aq) or LiAlH4(ether).
Reduction of ketones to secondary alcohols. EXAMPLE AND CONDITIONS.
Propanone+2[H]—>Propan-2-ol.
Conditions= NaBH4(aq) or LiAlH4(ether).
Reduction of carboxylic acids to primary alcohols. EXAMPLE AND CONDITIONS.
Ethanoic acid+4[H]—>Ethanol+H2O.
Conditions= LiAlH4(ether).
Hydrolysis of esters (with drops of acid vs with drops of alkali).
with drops of acid… just alcohols and carboxylic acids will form.
with drops of alkali…alcohols will form and carboxylic acids will form and react with alkali to form metal carboxylate salts and water.
Oxidation of primary alcohols to aldehydes. EXAMPLE AND CONDITIONS.
Ethanol+[O]—>Ethanal+H2O. Reflux and distill.
Conditions= H+/K2Cr2O7(VI) or H+/KMnO4(VII), reflux and distill to remove ethanal.
Oxidation of primary alcohols to carboxylic acids. EXAMPLE AND CONDITIONS.
Ethanol+[O]—>Ethanoic acid+H2O. Reflux only.
Conditions= H+/K2Cr2O7(VI) or H+/KMnO4(VII), reflux for over 1 hour.
Oxidation of secondary alcohols to ketones. EXAMPLE AND CONDITIONS.
Propan-2-ol+[O]—>Propanone+H2O.
Conditions= H+/K2Cr2O7(VI) or H+/KMnO4(VII), reflux.
Dehydration of alcohols. EXAMPLE AND CONDITIONS.
Ethanol—>Ethene+H2O.
Conditions= Hot Al2O3/Hot pumice.
Esterification reaction (type=condensation reaction). EXAMPLE AND CONIDTIONS.
Ethanol+Ethanoic acid⇌Ethyl ethanoate+H2O.
Conditions= Heat and concentrated H2SO4 and reflux.