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Practice flashcards covering the nomenclature, classification, properties, industrial production, and chemical reactions of alcohols based on the provided lecture notes.
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Alcohol (General Formula)
Alcohols have the functional group −OH attached to a hydrocarbon chain, with the general formula CH2OH (note: commonly CnH2n+1OH) or shortened to ROH.
Primary (1∘) Alcohols
Alcohols where the carbon with the −OH group is attached to one R group (two hydrogen atoms), or in the case of methanol, no R groups.
Secondary (2∘) Alcohols
Alcohols where the −OH group is attached to a carbon with two R groups and one hydrogen atom.
Tertiary (3∘) Alcohols
Alcohols where the carbon bonded to the −OH group is attached to three R groups and has no hydrogen atoms.
Glycerol
The common name for propane-1,2,3-triol, which can be obtained from fats and oils in living organisms.
Antifreeze
A substance containing ethane-1,2-diol added to vehicle cooling systems to prevent the coolant from freezing at winter temperatures.
C−O−H bond angle
An angle of approximately 105∘ (or 104.5∘) in alcohols, narrowed from the tetrahedral 109.5∘ due to repulsion between two lone pairs on the oxygen atom.
Hydration of Ethene
An industrial method for producing ethanol by reacting ethene with steam using a phosphoric acid catalyst.
Fermentation
The process of converting carbohydrates from plants into ethanol and carbon dioxide using enzymes from yeast at a temperature of about 35∘C in anaerobic conditions.
Biofuel
A fuel derived or produced from renewable biological sources.
Carbon-neutral fuel
A fuel where the carbon dioxide released during combustion is balanced by the carbon dioxide absorbed by the plant during photosynthesis, such as ethanol made by fermentation.
Elimination reaction
A reaction where a small molecule, such as water, leaves the parent molecule; in alcohols, these are always dehydrations.
Dehydration
A process where alcohols are heated with excess hot concentrated sulfuric acid or passed over heated aluminium oxide (Al2O3) at 600K to form an alkene and water.
Potassium Dichromate (VI)
An oxidising agent acidified with dilute sulfuric acid that changes from orange (Cr(VI)) to green (Cr(III)) when reacting with primary or secondary alcohols.
Aldehydes
The first oxidation product of primary alcohols, characterized by the functional group RCHO; they are named using the suffix -al.
Ketones
The oxidation product of secondary alcohols, characterized by the carbonyl group C=O within the body of the hydrocarbon chain (RCOR′); they are named using the suffix -one.
Carboxylic Acids
The product of the complete oxidation of primary alcohols, characterized by the functional group RCOOH.
Reflux
A laboratory technique where vapour condenses and drips back into the reaction flask to allow prolonged heating without loss of volatile reactants or products.
Distillation
A process used to separate substances based on different boiling points; for example, separating ethanal (294K) from an oxidation mixture before it turns into ethanoic acid.
Tollens' reagent
A solution of silver nitrate in aqueous ammonia used to test for aldehydes; a positive result forms a silver mirror as Ag+ ions are reduced to metallic Ag.
Fehling's solution
A blue solution containing copper(II) complex ions that forms a brick-red precipitate of copper(I) oxide when warmed with an aldehyde.
Carbonyl group
The C=O group found in both aldehydes and ketones.