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Chemistry Unit 5-specific Reactions

J000D97 Chemistry A2 level English 4.0Average rating 4.0 out of 5 (1 rating) 82 cards

Chemistry Unit 5-specific Reactions

Cards in this deck (82)

  1. 1Potassium manganate 1/2 equation\(KMnO_4^-\) + 8 \(H^+\) + 5\(e^-\) --> \(Mn^{2+}\) + 4\(H_2O\)
  2. 2Ethanedioic acid half equation\(C_2O_4^{2-}\) --> 2\(CO_2\) + 2\(e^-\)
  3. 3Thiosulphate half equation2\(S_2O_3^{2-}\) --> \(S_4O_6^{2-}\) + 2\(e^-\)
  4. 4Iodine half equation\(I_2\) + 2\(e^-\) --> 2\(I^-\)
  5. 5Bleach half equation\(ClO^-\) + 2\(H^+\) + 2\(e^-\) --> \(Cl^-\) + \(H_2O\)
  6. 6Forming copper (I) iodide solid equation2\(Cu^{2+}\) + 4\(I^-\) --> 2CuI + \(I_2\)
  7. 7Oxidation of methanol\(CH_3OH\) + \(H_2O\) ---> \(CO_2\) + 6\(H^+\) + 6\(e^-\)
  8. 8Dichromate breathalyser testadd in with a photo
  9. 9Combustion of benzene2 benzene + 15\(O_2\)
    -->
    12\(CO_2\) + 6\(H_2O\)
  10. 10Benzene + 3\(Br_2\) in the light goes to... Name the meachnism1, 2, 3, 4, 5, 6-hexabromocyclohexane
    Free-radical addition
  11. 11Benzene plus \(Br_2\) in the dark goes to... And name the mechanism and any other reactants or conditionsBromobenzene + HBr
    Electrophillic substitution
    Needs a halogen carrier \(FeBr_3\) or Fe
    Reflux
  12. 12How is a halogen carrier regenerated and from what?\(AlCl_4^-\) + \(H^+\) --> \(AlCl_3\) + HCl
  13. 13Nitration of benzene reaction and conditionsBenzene w/ conc. nitric and sulpuric acid
    Produces nitrobenzene and water
    50 degrees
  14. 14What is the name and formula of the electrophile used in nitration of benzene?Nitronium ion
    \(NO_2^+\)
  15. 15How is a nitronium ion formed?How is a nitronium ion formed?
  16. 16Sulfonation of benzene overall reaction, conditions and mechanismBenzene + fuming sulphuric acid
    -->
    Benzene sulphonic acid + \(H_2O\)
    Room temperature
    Electrophillic substitution
  17. 17What is fuming sulphuric acid?Sulphuric acid with additional sulphur trioxide in it.
  18. 18What are 2 types of Friedel-craft's reactions?Alkylation and acylation
  19. 19Overall reaction for alkylation of benzene and what is the mechanism?R-Cl + benzene
    -->
    R-benzene + HCl
    Electrophillic substitution
  20. 20Overall reaction for acylation of benzene and mechanism?RC=O-Cl + Benzene
    -->
    phenyl ketone + HCl
    Electrophillic substitution
  21. 21What is the name of the electrophile in acylation of benzene?Acylium ion
  22. 22By what mechanism is poly(phenylethene) produced?Addition polymerisation of phenylethene
  23. 23What is the mechanism for benzene to cyclohexane and what catalyst is used?Addition
    Raney Nickel catalyst
  24. 24Benzene + 3 \(H_2\) --> And at what temperature?Cyclohexane and 150 degrees
  25. 25Is phenol activating or deactivating?Activating
  26. 26Phenol + bromine water --> Reaction, mechanism, conditions2, 4, 6-tribromophenol + 3HBr
    Multi-electrophillic substitution
    No heating needed or halogen carrier
  27. 27What is observed when phenol is reacted with bromine water?The bromine water is decolourised
    A white precipitate smelling of antiseptic forms
  28. 28What is TCP and what is it used for?Trichlorophenol
    Antiseptic
  29. 29How can you make TCP?Phenol + 3 \(Cl_2\) (aq)
  30. 30Phenol + (3) dil. nitric A2, 4, 6-trinitrophenol (s) + 3 \(H_2O\)
  31. 31What reagent/s are used for nitration of phenol?Only dilute nitric acid is needed.
  32. 32Benzene with potassium manganate does what?It will oxidise any hydrocarbon side chain to an acid group, as well as benzaldehyde.
  33. 33What does \(NH_2\) do to benzene ring?Activates it
  34. 34Describe a tetramethylamine ion3 methyl group attached to a central N with a positive charge.
  35. 35ethylamine + HClethylammonium chloride
  36. 36What type of salts do amines produce with HCl?Ammonium chloride salts
  37. 37Amine + acid -->ammonium salt
  38. 38How many phenylamines are there in a copper complex with water?2
  39. 39How many methyl amines are involved in a copper complex with water?4
  40. 40What is a stronger base, a primary alkyl amine or ammonia and why?The primary alkyl amine because the methyl group is electron donating and enhances N's lone pair
  41. 41Which is a stronger base, phenyl amine or ammonia and why?Ammonia because \(NH_2\) on the benzene donates electrons to the delocalised ring structure which decreases N's lone pair electron density.
  42. 42What is notable about the sulfonation of benzene?It is reversible
  43. 43Can phenyl amine form salts? (give details)Yes
    Only with strong acids to drive the equilibrium to the right
    Forms phenylammonium salts
  44. 44Acyl chloride + amineHCl + N-substituted amide
  45. 45Chloromethane + methyl amine Mechanism and productsDimethylamine + HCl
    Nucleophillic substitution
  46. 46Ethanoyl chloride + phenyl amine...HCl + N-phenylethanamide
  47. 47When phenol is nitrated what is the ratio of 2:4 nitrophenol?2:1
  48. 484-aminophenol + ethanoic anhydride And give the mechanismEthanoic acid + paracetamol
  49. 49Reduction of nitrobenzene overall reactionnitrobenzene + 3 \(H_2\)
    --> w/ Sn/HCl
    Phenylamine + 2 \(H_2O\)
  50. 50Formation of nitrous acidFormation of nitrous acid
  51. 51Amine + nitrous acid --> Reaction and conditionsAlcohol + \(N_{2(gas)}\) + \(H_2O\)
    T<5\(\omicron\)
  52. 52How would you convert an amine into an alcohol?React with nitrous acid below 5\(\omicron\)
  53. 53Phenyl amine + nitrous acid T > 5\(\omicron\)Phenol + \(N_{2(gas)}\) + \(H_2O\)
  54. 54Phenyl amine + nitrous acid + HCl T < 5\(\omicron\)benzenediazonium ion + 2 \(H_2O\)
  55. 55Can you form benzenediazonium ions from aliphatic amines?No, because they are so unstable they decompose even at low temperatures.
  56. 56Can you form benzenediazonium ions from aromatic amines?Yes
  57. 57How do you form a benzenediazonium ion? And what by product is produced?Phenylamine + \(HNO_2\) + HCl
    2 \(H_2O\) molecules
  58. 58Between what 2 things does a coupling reaction happen?Phenol and benzenediazonium chloride
  59. 59Conditions for coupling reactionCold & alkaline
  60. 60benzenediazonium chloride + phenolazobenzene + HCl
  61. 61Where is the positive charge on a benzenediazonium ion?The inside N
  62. 62How many bonds are there between the N's of a benzenediazonium chloride?3
  63. 63How many bonds are there between the N's of an azo dye?2
  64. 64Acyl chloride + ammoniaAmide + HCl
  65. 65Polyesters are formed by what type of polymerisation?Condensation
  66. 66Polyamides are formed by what type of polymerisation?Condensation
  67. 67Polypeptides are formed by what type of polymerisation?Condensation
  68. 68What type of polymer is PET?A polyester
  69. 69What type of polymer is Nylon?A polyamide
  70. 70What type of polymer is Kevlar?A polyamide
  71. 71Poly(propenamide) is formed by which type of reaction?Addition
  72. 72Poly(ethenol) is formed by which type of reaction?Addition polymerisation
  73. 73Ninhydrin + amino acid -->Ammonia + hydrindatin + aldehydes + \(CO_2\)
  74. 74How is Ruheman's purple pigment produced?Hydrindatin reacting with ammonia
  75. 75Is phenol solution acidic or alkaline?Acidic because OH is activating so the OH bond is more polar
  76. 76Phenol + oxidising agentNo change as phenol is not readily oxidised
  77. 77How would you add a carbon to a chain?R-X (haloalk) + KCN
    Reflux in alkaline sol
    RCN + KX
  78. 78How would you add a carbon to aromatic molecules?Freidel-Craft's alkylation
  79. 79Hofmann's degradation reactionHofmann's degradation reaction
  80. 80Hofmann's degradation conditionsHeat
  81. 81Hunsdieker reactionHunsdieker reaction
  82. 82Conditions of Hunsdieker reactionReflux in \(CCl_4\)

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Doesn't include complexes or synthesis prep Only some redox. Mainly organic Note to self : put preparation reactions on a poster.
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