RBSE SS Chemistry study materials
RBSE SS Chemistry study resources

RBSE SS Chemistry flashcards

RBSE SS Chemistry · Build recall with a focused review session.

32 cards. Read the term and the definition here. The deck at the top of this page is optional.

Schottky defect
A point defect in ionic solids in which one cation and one anion are missing from their lattice sites, decreasing the density of the crystal.
Frenkel defect
A point defect in which an ion leaves its lattice site and occupies an interstitial position, so the crystal density remains unchanged.
Raoult's law
For an ideal solution, the partial vapour pressure of each volatile component equals its mole fraction multiplied by the vapour pressure of the pure component at that temperature.
van't Hoff factor
The ratio of the observed colligative property to the value calculated for the same molar concentration assuming no dissociation or association; i is greater than one for dissociation.
Azeotrope
A liquid mixture that boils at constant temperature without changing composition, because its vapour has the same composition as the liquid; ethanol-water is a minimum-boiling example.
Nernst equation
It relates electrode potential to standard potential and reaction quotient: E = E° minus (0.0591/n) log Q at 298 K for a reaction involving n electrons.
Kohlrausch law
At infinite dilution, the molar conductivity of an electrolyte equals the sum of the limiting ionic conductivities of its ions multiplied by their stoichiometric coefficients.
Fuel cell
An electrochemical cell that converts the chemical energy of a continuously supplied fuel, such as hydrogen, and an oxidant directly into electrical energy with high efficiency.
Order of reaction
The sum of the powers of the concentration terms in the experimental rate law; it may be zero, fractional or negative and is not obtained from the balanced equation.
Half-life
The time required for the concentration of a reactant to fall to one half of its initial value; for a first-order reaction it equals 0.693 divided by k.
Activation energy
The minimum extra energy that colliding reactant molecules must possess to form products; a catalyst provides an alternative pathway with a lower activation energy.
Inert pair effect
The tendency of heavier p-block elements to show an oxidation state two units lower than the group maximum, because the ns² pair becomes reluctant to participate in bonding.
Allotropy
The existence of an element in two or more different structural forms in the same physical state, such as rhombic and monoclinic sulphur or white and red phosphorus.
Lanthanoid contraction
The steady decrease in atomic and ionic radii from lanthanum to lutetium caused by poor shielding by the increasing 4f electrons, making later lanthanoids smaller.
Transition element
An element whose atom or common ion has an incomplete d subshell; this explains variable oxidation states, colour, catalysis and complex formation.
Spin-only magnetic moment
The magnetic moment calculated from the number of unpaired electrons n using μ = √(n(n+2)) Bohr magnetons, ignoring orbital contribution.
Chelate effect
The extra stability of a complex formed by a polydentate ligand compared with a similar complex of monodentate ligands, largely due to favourable entropy of chelation.
Crystal field splitting
The energy separation Δo between the lower t₂g and higher e_g d orbitals when ligands approach a metal ion in an octahedral complex.
SN2 mechanism
A one-step nucleophilic substitution in which the nucleophile attacks the carbon from the side opposite the leaving group, giving inversion of configuration.
Sandmeyer reaction
The reaction of a diazonium salt with copper(I) chloride or bromide in the corresponding acid to form an aryl chloride or bromide with loss of nitrogen.
Lucas test
A test that distinguishes alcohols by the time taken to form a cloudy layer with concentrated hydrochloric acid and zinc chloride: tertiary fastest, primary slowest.
Williamson synthesis
The preparation of an ether by treating a sodium alkoxide with a primary alkyl halide through an SN2 reaction; tertiary halides give elimination instead.
Aldol condensation
The base-catalysed reaction of two carbonyl compounds having α-hydrogens to form a β-hydroxy aldehyde or ketone, which may lose water to give an α,β-unsaturated product.
Cannizzaro reaction
The disproportionation of an aldehyde lacking α-hydrogens in concentrated alkali, producing equal amounts of a carboxylate salt and a primary alcohol.
Hofmann bromamide reaction
The treatment of an amide with bromine and sodium hydroxide to give a primary amine containing one carbon atom fewer than the original amide.
Carbylamine test
A test for primary amines in which heating with chloroform and alcoholic potassium hydroxide produces a foul-smelling isocyanide.
Denaturation
The loss of the secondary, tertiary and quaternary structure of a protein by heat or pH change, without hydrolysis of its peptide bonds.
Reducing sugar
A carbohydrate that has a free aldehyde or ketone group and therefore reduces Tollens' or Fehling's reagent; glucose, fructose and maltose are examples.
Addition polymerisation
A polymerisation in which unsaturated monomers join through their double bonds without eliminating any small molecule, as in the formation of polyethylene.
Vulcanisation
The heating of natural rubber with sulphur to form sulphur cross-links between polymer chains, increasing strength, elasticity and resistance to temperature.
Antiseptic
A chemical applied to living tissue, such as skin or wounds, to kill or inhibit microorganisms; examples include iodine and dilute phenol.
Micelle
A spherical aggregate of soap or detergent molecules in water, with hydrophobic tails pointing inward and hydrophilic heads outward, which solubilises grease.