4.2.3 Organic synthesis Flashcards

(32 cards)

1
Q

what does a basic set of quickfit apparatus include

A
  • round-bottom / pear-shaped flask
  • receiver
  • screw-tap adaptor
  • condenser
  • still head
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2
Q

how do you set up apparatus for reflux

A
  • reaction mixture + anti-bumping granules added to flask
  • apply grease (vaseline) to joint of condenser + put into flask
    > condenser in upright poistion
    > water out at top + water in at bottom
  • condenser clamped loosely to clamp stand
  • flask heated
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3
Q

why are anti-bumping granules used for reflux

A
  • so contents boil smoothly
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4
Q

what are benefits of reflux heating

A
  • prevents volatile components from escaping + flask from boiling dry
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5
Q

how does reflux heating work

A
  • vapour from mixture rises up inner tube of condenser until it meets outer jacket containing cold water
  • vapour condenses + drips back into flask
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6
Q

why must there be no stopper on top of condenser under reflux

A
  • you make a close system + pressure will build up ad heated air expands
    > can lead to apparatus exploding
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7
Q

what is distillation used for

A
  • separating a pure liquid from its impurities
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8
Q

how do you set up the apparatus for distillation

A
  • flask clamped by neck
    > still head attached to flask (T shaped + has 2 ground-glass joints)
    > condenser attached to still head adaptor + screw cap adaptor (with thermometer)
  • second clamp around receiver adaptor which attached to condenser
  • water enters at lower end + leavs at top
  • flask used to collect distillate
  • flask heated
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9
Q

how does heating under distillation work

A
  • diff liquids in mixture have diff bp
    > liquid with lowest bp is most volatile + boils first
  • vapour moves out flask + reaches cold condenser, condenses + becomes liquid
    > liquid drips into collecting flask
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10
Q

what are the different ways you can heat up compounds when using reflux or distil apparatus

A
  • bunsen burner
  • water bath (less than 100)
  • heating mantle for flammable liquids
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11
Q

how can you purify organic products using separating funnel

A
  • pour mixture of liquids into separating funnel
  • tap is closed + invert to mix contents
  • allow layers to settle
  • place conical flask under separating tunnel, remove stopper, open tap, until whole of lower layer has left funnel
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12
Q

how can you remove any acid impurities from your impure product

A
  • add aqueous sodium carbonate + shake mixture in separating funnel
    > any acid present will react with sodium carbonate releasing CO2 gas
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13
Q

what to do if there is any water left in an organic product

A
  • add drying agent
    > anhydrous inorganic salt that readily takes up water to become hydrated
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14
Q

name some drying agents

A
  • anhydrous magnesium sulfate (Mg SO4): general drying
  • anhydrous calcium chloride (CaCl2): drying hydrocarbons
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15
Q

give the procedure for drying an organic liquid

A
  • add drying agent to liquid + swirl to mix contents
  • add stopper to prevent evaporation of products + leave for 10 mins
  • if solid stuck together in lump, there is still water present
    > add more drying agent until some solid is dispersed in the solution as fine powder
  • pour liquid from solid in another flask + if liquid dry it should be clear
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16
Q

what is a sign that the organic product is dry

A
  • the liquid should be clear
17
Q

what is redistillation

A
  • if organic liquids have similiar bp then prepared sample may have impurities
    > distillation clean + dry + set up again so 2nd distillation is carried out
    > this time only collect product with bp of compound you are trying to make
18
Q

what is organic synthesis

A
  • preparation of complex molecules from simple starting molecules
19
Q

what are target molecules

A
  • compound that chemist is trying to prepare by organic synthesis
20
Q

to convert a starting molecule into target molecules you need to carry out the 2 stage synthesis which includes:

A
  • identifying functional groups in your starting + target molecules
  • identifying the intermediate that links the starting + target molecules
  • state the reagents + conditions for each step
21
Q

state the reagents + conditions needed to convert from an alkane to a haloalkane

A
  • halogen
  • UV light
  • free radical substitution
22
Q

state the reagents + conditions needed to convert from an alkene to a haloalkane

A
  • hydrogen halide
  • room temp
  • electrophilic addition
23
Q

state the reagents + conditions needed to convert from an alkene to an alkane

A
  • H2
  • nickel catalyst
  • 150C
  • 5 atom
  • addition
24
Q

state the reagents + conditions needed to convert from a haloalkane to an alcohol

A
  • aqueous alkali (NaOH)
  • reflux
  • nucleophilic substitution
25
state the reagents + conditions needed to convert from an alkene to an alcohol
- H3PO4 catalyst - H2O - reflux
26
state the reagents + conditions needed to convert from an alcohol to an alkene
- conc H2SO4 - elimination
27
state the reagents + conditions needed to convert from an alcohol to a haloalkane
- sodium halide - H2SO4 - reflux - substitution
28
state the reagents + conditions needed to convert from an to an
29
state the reagents + conditions needed to convert from an alcohol to an aldehyde
- primary alcohol - distil - partial oxidation - acidified potassium dichromate
30
state the reagents + conditions needed to convert from an alcohol to a ketone
- secondary alcohol - reflux - acidified potassium dichromate
31
state the reagents + conditions needed to convert from an aldehyde to a carboxylic acid
- oxidation
32