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Flashcards

Chemistry Unit 5 Flashcards: Organic Synthesis

J000D97 Chemistry A2 level Inglês 30 flashcards

Flashcards do conjunto (30)

  1. 1List 3 artificial sweetenersSaccharin
    Cyclamate
    Aspartame
  2. 2Burns with a smoky yellow flameBenzene
  3. 3Decolourises bromine waterAlkene
  4. 4Produces carbon dioxide when reacted with a metal carbonateCarb A
  5. 5White fumes when reacted with \(PCl_5\)OH group
  6. 6Yellow-orange ppt when reacted w/ 2,4-DNPHCarbonyl group (not a Carb A)
  7. 7Red-brown ppt with Fehling's or BenedictsAldehyde
  8. 8Silver mirror w/ \(AgNO_3\) + \(NH_{3(aq)}\)Aldehyde
  9. 9Antiseptic pale yellow crystals w/ \(I_2\) /NaOH\(CH_3\)-C=O
    Or something which oxidises to it
  10. 10Is phenol solution neutral, alkaline or acidic? Why?Acidic b/c O's LP is pushed into benzene's delocalised ring structure making the OH bond more polar so it loses \(H^+\)
  11. 11Can phenol be oxidised?No, it is not readily oxidised
  12. 122 reactions which increase chain lengthReflux w/ HCN/KCN
    Friedel-Craft's alkylation
  13. 13Names of the 2 reactions which decrease chain lengthHofmann's degradation
    Hunsdiecker reaction
  14. 14Define: hazardPotential to do harm
  15. 15Define: riskLikelihood of harm
  16. 16List 4 precautionary measures that can be taken to reduce riskUse a fume cupboard
    Reduce scale
    Look for an alternative safer route
    Replace a reactant w/ a less toxic alternative
  17. 172 ways of separating isomersThin-layer chromatography
    Electrophoresis
  18. 182 ways to make single isomersAsymmetric synthesis
    Use of chiral auxiliaries
  19. 19Describe combinational chemistryAN automated process by which many compounds all similar to a 'lead' compound are produced very quickly to see if they have lower side effects or more medical benefits as drugs than current treatments. They are all tested and then possibles kept in a large digital library.
  20. 20What is a solid phase reaction?Compounds are bonded to polystyrene-based polymer beads and the reaction takes place on them. The product remains bonded to the beads and excess reactants can be washed away.
  21. 21Why are sold phase reactions using polymer beads useful?Because 1 end of the reactant mol is fixed so all reactions have to happen at one end.
  22. 22What do you heat with during reflux?An electric heater
  23. 23What can be added to remove acid?\(NaHCO_3\)
  24. 24What is solvent extraction?When you add a solvent to a product in another solvent and the product is more soluble in the new solvent. When shaken it dissolves in the added solvent leaving impurities in the original layer, and a separating funnel can be used to tap off the lower layer, separating the product from another impurity or unwanted product which is more soluble in the other solvent.
  25. 25Describe re-crystalisationAdd hot solvent till solid just dissolves
    Let solution cool slowly
    Crystals will form but impurities won't fall out of solution because they aren't near saturation.
    Remove the crystals by filtration and wash them with minimal ice cold solvent
    Leave to dry.
  26. 26What can you add to remove water from a mixture?\(CaCl_2\) granules
  27. 27What are inside fractional distillation columns?Glass beads
  28. 28How do you determine melting point?Put solid in capillary tube
    Place in oil w/ thermometer
    Slowly heat and stir
    Read the temperature when the solid just melts.
  29. 29How do you make cholesteryl benzoateDissolve cholesterol in pyridine
    Add benzoyl chloride
    Heat in a steam bath for 10 mins
    Cool and add methanol
    Filter off crystals of ester and wash with methanol
    Recrystallise using ethyl ethanoate as a solvent.
  30. 30How do you make methyl-3-nitrobenzoate?Dissolve methyl benzoate in cold conc sulphuric
    Add 50/50 mix of conc nitric and sulphuric dropwise constantly stirring.
    Stir for 15 mins
    Pour over crushed ice
    When melted filter off crystals
    wash with water
    re-crystallise w/ ethanol

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A2 level Chemistry (Unit 5) FlashCards sobre Chemistry Unit 5 Flashcards: Organic Synthesis, criado por J000D97 em 05-04-2015.
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J000D97
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