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Flashcards covering the classification, naming, physical properties, production, and chemical reactions of alcohols based on the provided lecture notes.
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General formula of an alcohol
CnH2n+1OH (often shortened to ROH).
Hydroxyl group
The −OH functional group attached to a hydrocarbon chain.
Primary (1∘) alcohol
An alcohol where the carbon atom bonded to the −OH group is attached to one R group (and therefore two hydrogen atoms).
Secondary (2∘) alcohol
An alcohol where the −OH group is attached to a carbon atom with two R groups (and therefore one hydrogen atom).
Tertiary (3∘) alcohol
An alcohol where the carbon atom bonded to the −OH group is attached to three R groups (and therefore no hydrogen atoms).
Ethanol health effects
A nervous system depressant that interferes with nerve impulse transmission; in large amounts, it leads to loss of balance, impaired vision, and can be fatal.
C−O−H bond angle
Approximately 105∘ (or 104.5∘) because the presence of two lone pairs on the oxygen atom repels bonding pairs, squeezing the angle down from the perfect tetrahedral 109.5∘.
Glycerol
The common name for propane-1,2,3-triol, often obtained from fats and oils.
Ethane-1,2-diol
The main ingredient in most antifreezes used in motor vehicle cooling systems.
Alcohol solubility
Short-chain alcohols are soluble in water due to hydrogen bonding; solubility decreases as the non-polar hydrocarbon chain lengthens and dominates.
Hydration of ethene
An industrial method of producing ethanol by reacting ethene (from cracked crude oil) with steam using a phosphoric acid catalyst.
Fermentation of ethanol
The process where carbohydrates from plants are broken down into sugars and converted into ethanol by yeast enzymes under anaerobic conditions at about 35∘C.
Biofuel
A fuel derived or produced from renewable biological sources.
Carbon-neutral fuel
A fuel, such as ethanol from fermentation, where the CO2 released during combustion and production is balanced by the CO2 absorbed by the plants during photosynthesis.
Methylated spirits
Ethanol with a small amount of poisonous methanol and a purple dye added to make it undrinkable and tax-free for use as a fuel.
Elimination reaction (Dehydration)
A reaction where a water molecule is removed from an alcohol (using an −OH group and a hydrogen from an adjacent carbon) to form an alkene.
Oxidising agent for alcohols
Acidified potassium dichromate(VI), which changes colour from orange (Cr(VI) ions) to green (Cr(III) ions) upon reduction.
Oxidation of primary alcohols
Oxidised to aldehydes (RCHO) via distillation or further oxidised to carboxylic acids (RCOOH) via reflux.
Oxidation of secondary alcohols
Oxidised to ketones (R2CO) which are not easily oxidised further.
Oxidation of tertiary alcohols
Not easily oxidised because the reaction would require breaking a stable C−C bond.
Reflux
A laboratory technique where vapour condenses and drips back into the reaction flask, allowing prolonged heating to ensure complete oxidation.
Tollens' reagent test
A test using silver nitrate in aqueous ammonia that forms a 'silver mirror' when warmed with an aldehyde, but shows no reaction with ketones.
Fehling's test
A test using blue copper(II) complex ions that form a brick red precipitate of copper(I) oxide when warmed with an aldehyde.