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substitution of alkanes and halogens
(in the presence of UV light and/or heat) saturated hydrocarbon (alkanes) + halogens = haloalkane
Substitution of primary haloalkanes and an alkali
(In the presence of NaOH and heath) primary haloalkane + alkali = alcohol
Substitution of primary haloalkanes and ammonia
(in ethanol) Primary haloalkane + ammonia = primary amine
substitution of primary haloalkanes and water
haloalkane + water = alcohol + hydrogen halide
substitution of primary alcohols and ammonia
(using alumina catalyst and heat) primary alcohol + ammonia = primary amine + water
Process of addition between alkenes and other molecules
carbon to carbon double bonds are broken to allow the molecule to add other atoms or groups, creating one product from 2 or more reactants
Hydrogenation
(using nickel as a catalyst) alkene + hydrogen (H2) = alkane
Halogenation
alkene + halogen = dihaloalkane
Hydration
(with conc phosphoric acid catalyst and heat and high pressure) alkene + water vapour = alcohol
Polymerisation
alkene monomer + alkene monomer = alkane polymer
Hydrolosis
water is a reactant and is used to break bonds in a molecule to produce new compounds
Hydrolosis of an ester
(with excess H+, heat, and dilute H2SO4) ester + water = acid + alcohol
Esterification (a condensation reaction)
(with conc. sulfuric acid catalyst) carboxylic acid + alcohol = water + ester
primary alcohol to carboxylic acid (oxidation reaction)
alcohol → aldehyde → carboxylic acid (with either MnO4 or Cr2O72- and H+)
To get the aldehyde not the carboxylic acid:
limit the amount of heat
limit the oxidising agent
remove the aldehyde as its produced via distillation
amino acids
the monomers of proteins (amino group + carboxyl group + alpha carbon + side chain)
monosaccharides
building blocks of starch
glycosidic/ether link
link that forms between two sugar rings