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F322 KEY WORDS

sophiewalkerrock Chemistry A Level Inglés 76 fichas

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  1. 1Addition PolymerA very long molecular chain formed by repeated addition reactions of many unsaturated alkene molecules ( monomers)
  2. 2Addition PolymerisationThe process in which monomers add on to a growing chain one at a time to form a very long saturated molecule chain (addition polymer)
  3. 3Addition ReactionA reaction in which a reactant is added to an unsaturated molecule to make a saturated molecule.
  4. 4Alicyclic hydrocarbonA hydrocarbon with carbon atoms joined together in a ring structure
  5. 5Aliphatic hydrocarbonA hydrocarbon with carbon atoms joined together in straight or branched chains.
  6. 6AlkanesThe homologous series with the general formula:
  7. 7Atom EconomyMolecular mass of desired product/sum of molecular masses of all products
  8. 8Alkyl GroupAn alkane with a hydrogen atom removed e.g.CH3
  9. 9Biodegradable materialA substance that is broken down naturally in the environment by living organisms.
  10. 10Carbocationis an organic ion in which a carbon atom has a positive charge.
  11. 11CatalystA substance that increases the rate of a chemical reaction without being used up in the process.
  12. 12Cis-trans isomerisationSpecial type of E/Z isomerism, which there is a non-hydrogen group and a hydrogen on each C of the C=C. Cis (Z) isomer has the H atoms on the same side. Trans (E) isomer has the H atoms on opposite sides.
  13. 13CrackingRefers to the breaking down of long-chained saturated hydrocarbons to form a mixture of shorter-chained alkanes and alkenes.
  14. 14Curly ArrowA symbol used in a reaction mechanism to show the movement of an electron pair in the formation or breaking of a covalent bond.
  15. 15DehydrationAn elimination reaction in which water is removed from a saturated molecule to make an unsaturated molecule.
  16. 16Displayed formulaShows the relative positioning of all of the atoms in a molecule and the bonds between them.
  17. 17ElectrophileAn atom that is attracted to an electron-rich centre or atom, where it accepts a pair of electrons to form a new covalent bond.
  18. 18Electrophilic additionA type of addition reaction in which an electrophile is attracted to an electron-rich centre or atom, whee it accepts a pair of electrons to form a new covalent bond.
  19. 19Elimination ReactionRefers to the removal of a molecule from a saturated molecule to make an unsaturated molecule.
  20. 20EsterificationThe reaction of an alcohol with a carboxylic acid to produce an ester and water.
  21. 21E/Z isomerismA type of stereoisomerism in which different groups attached to each carbon of a C=C double bond may be arranged differently in space due to the restricted rotation of the C=C bond.
  22. 22Fractional DistillationThe separation of the components in a liquid mixture into fractions which differ in boiling points by means of distillation, typically using a fractionating column.
  23. 23FragmentationThe process in mass spectrometry that causes a positive ion to split into pieces, one of which is a a positive fragment ion.
  24. 24Functional GroupThe part of the organic molecule responsible for the chemical reactions.
  25. 25Heterolytic FissionThe breaking of a covalent bond with both of the bonded electrons going to one of the atoms, forming ions.
  26. 26Homologous SeriesA series of organic compounds with the same functional group but with each successive member differing by CH2
  27. 27Homolytic FissionBreaking of a covalent bond, with one of the bonded electrons going to each atom, forming two radicals.
  28. 28HydrocarbonsOrganic compounds that contain carbon and oxygen only.
  29. 29HydrolysisA reaction with water or aqueous hydroxide ions that breaks a chemical compound into two compounds.
  30. 30InitiationFirst step in a radical substitution in which the free radicals and generated by ultraviolet radiation.
  31. 31Limiting ReagentThe substance in a chemical reaction that runs out first.
  32. 32MechanismA sequence of steps chowing the path taken by electrons in a reaction.
  33. 33Molecular Ion, M+The positive ion formed in mass spectrometry when a molecule loses an electron.
  34. 34MonomerSmall molecule that combines with many other monomers to form a polymer.
  35. 35NucleophileAn atom that is attracted to an electron-deficient centre or atom, where it donates a pair of electrons to form a new covalent bond.
  36. 36Nucleophilic SubstitutionA type of substitution reaction in which a nucleophile is attracted to an electron deficient centre or atom, where it donates a pair of electrons to form a new covalent bond.
  37. 37Pi-bondReactive part of a double bond formed above and below the plane of the bonded atoms by sideways overlap of p-orbitals.
  38. 38PolymerA long molecular chain built up from monomer units.
  39. 39RadicalA species with an unpaired electron.
  40. 40Radical SubstitutionIs a type of substitution reaction in which a radical replaces a different atom or group of atoms.
  41. 41RefluxThe continual boiling and condensing of a reaction mixture to ensure that the reaction takes place without the contents of the flask boiling dry.
  42. 42Repeat UnitSpecific arrangement of atoms that occurs in the structure over and over again.
  43. 43Saturated HydrocarbonA hydrocarbon with single bonds only.
  44. 44Skeletal formulais a simplified organic formula, with hydrogen atoms removed from alkyl chains, leaving just a carbon skeleton and associated functional groups.
  45. 45StereoisomersCompounds with the same structural formula, but with a different arrangement of atoms in space.
  46. 46Structural FormulaShows the minimal detail for the arrangement of atoms in a molecule.
  47. 47Structural IsomersMolecules with the same molecular formula but with different structural arrangement of atoms.
  48. 48Substitution reactionA reaction in which an atom or group of atoms is replaced with a different atom or group of atoms.
  49. 49TerminationThe step at the end of a radical substitution when two radicals combine to form a molecule.
  50. 50Unsaturated hydrocarbonsA hydrocarbon containing carbon-carbon double bonds.
  51. 51VolatilityThe ease that a liquid turns into a gas. Volatility increases as boiling point decreases.
  52. 52% YieldActual amount, in mol, of product
  53. 53Enthalpy, HThe heat content that is stored in a chemical system.
  54. 54ExothermicRefers to a reaction in which the enthalpy of the products is smaller than the enthalpy of the reactants, resulting in heat loss to the surroundings.
  55. 55EndothermicRefers to a reaction in which the enthalpy of the products is greater than the enthalpy of the reactants, resulting in heat being taken in from the surroundings.
  56. 56Enthalpy Profile DiagramA diagram for a reaction to compare the enthalpy of the reactants with the enthalpy of the products.
  57. 57Activation EnergyThe minimum energy required to start a reaction by the breaking of bonds.
  58. 58Standard ConditionsA pressure of 100kPa (1atmosphere); a stated temperature, usually 298K (25C); a concentration of 1.0 moldm-3 (for reactions with aqueous solutions).
  59. 59Standard StateThe physical state of a substance under the standard conditions of 100kPa and 298K.
  60. 60Standard Enthalpy Change of CombustionThe enthalpy change that takes place when one mole of a substance reacts completely with oxygen under standard conditions, all reactants and products being in their standard states.
  61. 61Standard Enthalpy Change of FormationThe enthalpy change that takes place when one mole of compound is formed from the constituent elements in their standard states under standard conditions.
  62. 62Specific Heat CapacityThe energy required to raise the temperature of 1g of a substance by 1'C
  63. 63Bond EnthalpyThe enthalpy change that takes place when breaking by homolytic fission 1 mol of a given bond in the molecules of a gaseous species.
  64. 64Average Bond EnthalpyThe average enthalpy change that takes place when breaking by homolytic fission 1 mol of a given type of bond in the molecules of a gaseous species.
  65. 65Hess' LawStates that, if a reaction can take place by more than one route and the initial and final conditions are the same, the total enthalpy change is the same for each route.
  66. 66Enthalpy CycleA diagram showing alternative route between reactants and products which allows the indirect determination of an enthalpy change from other known enthalpy changes using Hess' Law.
  67. 67Rate of reactionThe change in concentration of a reactant or a product in a given time.
  68. 68Heterogeneous CatalysisA catalysis of a reaction in which the catalyst has a different physical state from the reactants; frequently, reactants are gases whilst the catalyst is a solid.
  69. 69Homogeneous CatalysisCatalysis of a reaction in which the catalstt and reactants are in the same physical state, which is most frequently the aqueous or gaseous state.
  70. 70Boltzmann DistributionThe distribution of energies of molecules at a particular temperature, often shown as a graph.
  71. 71Dynamic EquilibriumThe equilibrium that exists in a closed system when the rate of the forward reaction is equal to the rate of the reverse reaction.
  72. 72Le Chatelier's PrincipleStates that when a system in dynamic equilibrium is subjected to a change, the position of equilibrium will shift to minimise the change.
  73. 73Greenhouse EffectThe process in which the absorption and subsequent emission of infrared radiation by atmospheric gases warms the lower atmosphere and the planet's surface.
  74. 74TroposphereThe lowest layer of the Earth's atmosphere, extending from the Earth's surface to about 7km (above the poles) and to about 20km (above the tropics).
  75. 75StratosphereThe second layer of the Earth's atmosphere, containing the 'ozone layer', about 10km to 50km above the earth's surface.
  76. 76AbsorptionThe process that occurs when a gas, liquid or solute is held to the surface of a solid or, more rarely, a liquid.

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