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chem salters a2 reactions to learn

joannalivesey Inglês 5,0Avaliação média 5,0 de 5 (1 avaliação) 69 flashcards

chem salters a2 reactions to learn

Flashcards do conjunto (69)

  1. 1alkane -> halogenoalkanehalogen e.g. Cl2,
    UV light + RT
  2. 2alkene -> halogenoalkaneconc HBr (aq),
    RT+P
  3. 3alkene -> bromoalcoholshake with bromine water,
    RT+P
  4. 4alkene -> dihalogenoalkaneBr2 (in organic solvent),
    RT+P
  5. 5alkene -> alkaneH2 (g),
    Pt catalyst, RT+P OR
    Ni catalyst, 150˚C, 5atm
  6. 6alkene -> alcoholsteam,
    phosphoric acid catalyst, 300˚C, 60atm
  7. 7alkene-> addition polymertrace O2, 200˚C, 1500atm
    (addition polymerisation)
  8. 8homolytic fission of halogenoalkanesUV light
    makes radicals
  9. 9heterolytic fission of halogenoalkanesdissolve in polar solvent (e.g.water/ethanol mix)
    makes carbocation and halide ion
  10. 10halogenoalkane -> alcoholNaOH (aq), reflux
    OR
    water, reflux
  11. 11halogenoalkane -> amineconc NH3
    heat in a sealed tube
  12. 12halogenoalkane -> nitrile (R-CN) + halide ionreflux with NaCN in ethanol/water
    (given on exam data sheet)
  13. 13primary alcohol -> bromoalkaneconc H2SO4 and NaBr (s) to make HBr in situ, heat under reflux (given on exam data sheet)
  14. 14primary alcohol -> chloroalkaneconc HCl
  15. 15primary alcohol -> alkenepass vapour over Al2O3 at 300˚C
  16. 16primary alcohol -> aldehyde. (oxidation)acidified potassium dichromate,
    heat and distil off as formed
    (goes from orange to green as dichromate ions reduced)
  17. 17primary alcohol -> carboxylic acid. (oxidation)Acidified potassium dichromate,
    Heat under reflux
    (goes from orange to green as dichromate ions reduced)
  18. 18secondary alcohol -> ketone. (oxidation)Acidified potassium dichromate
    Heat under reflux
    (goes from orange to green as dichromate ions reduced)
  19. 19aldehyde -> primary alcohol. (reduction)NaBH4
    (given on exam data sheet)
  20. 20ketone -> secondary alcohol. (reduction)NaBH4
    (given on exam data sheet)
  21. 21aldehyde -> cyanohydrinHCN
    alkaline conditions
  22. 22ketone -> cyanohydrinHCN
    alkaline conditions
  23. 23aldehyde -> carboxylic acidacidified potassium dichromate, reflux (orange to green) OR
    heat with Fehlings solution (orange/brown precipitate formed)
  24. 24carboxylic acid -> esteralcohol, conc H2SO4, heat under reflux
  25. 25phenol -> esteracyl chloride RT+P (makes HCl) OR
    acid anhydride and heat under reflux (makes carboxylic acid)
    both anhydrous conditions
  26. 26ester hydrolysismod conc acid (e.g. H2SO4) OR mod conc alkali (e.g. NaOH)
    heat under reflux
  27. 27alkylation of a primary aminehalogenoalkene + primary amine -> secondary amine + HCl/HBr
  28. 28making primary amides (acylation)acyl chloride + conc NH3-> primary amide + HCl
  29. 29making secondary amides (acylation)acyl chloride + primary amine -> secondary amide + HCl
  30. 30amide hydrolysismod conc acid (e.g. HCl) OR mod conc alkali (e.g. NaOH)
    heat under reflux
  31. 31Benzene -> cyclohexaneH2, finely divided Ni catalyst, 300˚C, 30atm
  32. 32nitrobenzene -> phenylaminecatalyst: Sn + conc HCl, heat under reflux
    (on exam data sheet)
  33. 33phenyl amine -> benzenediazonium ion (diazotisation)dilute HCl, NaNO2 (to form nitrous acid HNO2), less than 5˚C
  34. 34diazonium ion -> azo compounddiazonium ion -> azo compound
  35. 35benzene nitrationnitrating mix- conc nitric acid, conc sulphuric acid, less 55˚C
  36. 36benzene sulfonationconc sulfuric, heat under reflux for several hours
  37. 37benzene chlorinationCl2 (g), anhydrous AlCl3, RT+P
  38. 38benzene BrominationBr2 (g), anhydrous FeBr3, RT+P
  39. 39benzene alkylationchloroalkane, anhydrous AlCl3, heat under reflux
  40. 40benzene acylationacyl chloride, anhydrous AlCl3, heat under reflux
  41. 41advantages of friedel-craftreactions can be carried out in ionic liquids-
    reduces solvent emission, reduces flammability, recycle easily and allow reactions to be carried out at reduced temps
  42. 42tests: alcohol + NaOHno reaction
  43. 43tests: phenol + NaOHreacts to form a salt
  44. 44tests: carboxylic acid + NaOHreacts to form a salt
  45. 45tests: alcohol + carbonateno reaction
  46. 46tests: phenol + carbonateno reaction
  47. 47tests: carboxylic acid + carbonatefizzes- releases CO2
  48. 48test for phenolneutral iron (III) chloride
    turns from yellow to purple
  49. 49[Fe(H2O)6]2+green solution
  50. 50[Fe(H2O)6]3+yellow solution
  51. 51Fe(OH)2(s)green gelatinous solid
  52. 52Fe(OH)3(s)orange gelatinous solid
  53. 53[Cu(H2O)6]2+blue solution
  54. 54[Cu(NH3)4(H2O)2]2+violet solution
  55. 55[CuCl4]2-yellow solution
  56. 56Cu(OH)2(s)pale blue solid
  57. 57N2Odinitrogen(I) oxide (nitrous oxide) colourless gas
  58. 58NO2nitrogen (IV) oxide (nitrogen dioxide)-brown toxic gas
  59. 59NOnitrogen (II) oxide (nitrogen monoxide)- colourless gas, free radical
  60. 60shape of N2linear
  61. 61shape of ammoniapyramid
  62. 62shape of ammonium iontetrahedral
  63. 63shape of nitrate (III) ionbent
  64. 64shape of nitrate (V) ionplanar triangular
  65. 65test for aldehydefehlings solution, brown/orange precipitate formed
  66. 66carboxylic acid -> aldehydereflux with dilute HCl
  67. 67carboxylic acid -> acyl chlorideSCl2O, heat under reflux
  68. 68nitrile -> carboxylic acidheat under reflux with dilute H2SO4
  69. 69coupling reactionalkali, less than 5˚C

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FlashCards sobre chem salters a2 reactions to learn, criado por joannalivesey em 29-04-2014.
Criado por
joannalivesey
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