chapter 16 organic synthesis Flashcards

1
Q

Why is it important that many organic reacctions are heated under reflux

A
  • many organic reactions occur to slowly at room temperature
  • common for organic reactions to be heated to overcome the activation energy and increase the rate of reaction
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2
Q

Why is heating under reflux used to produce an organic liquid

A
  • this prevents it boiling off the solvent reactants or products
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3
Q

Describe the procedure for heating under reflux and why each apparatus is needed

A
  • bunsen burner use to heat the reaction mixture - allowes reaction under reflux carried out at a fixed temperature
  • water bath used if reaction below 100 degrees celcius
  • if heating flammable liqudis heating mantle is used - provide safety incase of appartus leak or crack
  • anti bumping granules added to flask befor heating - contents boil smoothly if not use large bubbles form at bottom of liquid causing glassware to vibrate or jummp violently
  • never put a stopped - otherwise a closed system will be made and pressure will build up as heated air expnded cause apparatus to explode
  • water enters condenser at bottom and leaves at top to ensure outer jacket is full
    *
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4
Q

Why is heating under reflux used and how does it work

A
  • enables liquid to be continually boiled whilst the reaction takes place
  • prevents volatile components from escaping falsk and the flask from boiling dry
  • the vapour form the mixture rises up the innter tine of the condenser until it meets the outerjacket containing cold water
  • vapour then condenses and drips back into the flask
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4
Q

What is distillation

A

common method used to seperate a pure liquid from its impurities

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5
Q

Briefly describe distillation

A
  • flask is heated and mixture in the flask will start to boil
  • different liquids will have different boiling point the liquid with the lowest boiling point is most volatile
  • vapour moves out of flask into other parts of apparatus
  • when vapours reach fold condenser they become a liquid which drips into the collecting flask
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6
Q

Why do we need to purify organic liquids

A
  • water may be obtained with the product
  • top layer will be organic and bottom is aqueous / waater layer
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7
Q

How do we seperate the organic layer from the aqueous layers

A
  • ensure the tap of the seperating funnel is closed
  • pour the mixture of liquids into the seperating funnel and place the stopper on the top of the funnel and incert to mix the contents
  • allow layers to settle
  • add some water to see what layer increases in volume - the aqueou layer
  • place a conical flaks under the seperating funnel remove the stopped and open the tap until whole of lower layer has left the funnel
  • placre second conical flask under the seperating funnel to collet the other layer
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8
Q

How do you get rid of acid impurities

A
  • by adding aqueous sodium carbonate and shaking mixture in a seperating funnel
  • carbon dioxide will be produce tap needs to be slowlu opened holding the stoppeded seperating funnel upside down to release builfd up gas pressure
  • aqueous sodium carbonate lauer removed and organic layer is washed with water before running both layer into seperate flasks
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9
Q

Why do we add drying agents to organic products

A

remove traces of waater

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10
Q

name three drying agents

A
  • anhydrous calcium chlorice CaCL2 - drying hydrocarbons
  • anhydrous calcium sulfate CaSO4 - general drying
  • anhydrous magnesium sulfate - MgSO4 - general drying
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11
Q

Describe the procedure for drying an organic liquid

A
  • add organic liquid to a concial flask
  • add drying agnet to the liquid and swirl
  • place stopper on the flask prevent prouct evaportation leave for 10 minutes
  • if the solid has all stuck together in a lump there i still some water present add more drying agent until some solid is dispersed in the solution as a fine poweder
  • decant the iquid from the solid into another flask if liquid is dry it should be clear
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12
Q

How pure is the product with a narrower boiling range

A

the purer the product

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13
Q

What is the functional group for an alkene

A

C=C

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14
Q

What is the functional group for an alcohol

A

-OH

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15
Q

What is the functional group for an haloalkane

A

-Cl
-Br
-I

16
Q

What is the functional group for an aldehyde

A

C double bond O singe bond H

17
Q

What is the functional group for a ketone

A

C(CO)C

18
Q

What is the functional group for an carboxylic acid

A

COOH

19
Q

What is the functional group for an ester

A

COOC

20
Q

What is the functional group for an amine

A

NH2

21
Q

What is the functional group for an acyl chloride

A

COCl

22
Q

What is the functional group for a nitrile

A

CN

23
Q

How do you get from an alkane to a haloalkane

A

halogen
UV

24
Q

how do you get from an alkene to an alkane

A
  • H2
  • nickel catalyst
25
Q

How do you get from an alkene to a halohalkane

A
  • hydrogen halide
26
Q

How do you get from an alkene to an alcohol

A
  • H2O (g)
  • H3PO4 catalyst
27
Q

How do you get from an alcohol to an alkene

A

concentrated sulfuric acid

28
Q

How do you gt from a haloalkane to an alcohol

A

NaOH (aq)
reflux

29
Q

How do you get from an alcohol to a haloalkane

A
  • sodium halide
  • H2SO4
30
Q

How do you get from a alcohol to a carboxylic acid

A
  • primary alcohol
  • acidified K2Cr2O7
  • reflux
31
Q

How do you get from an alcohol to an aldehyde

A
  • primary alcohol
  • acidifieed K2Cr2O7
  • distil
32
Q

How do you get from an alcohol to a ketone

A
  • secondary alcohol
  • acidified K2Cr2O7
  • reflux
33
Q

How do you determine solubility of a compound

A

If it has an Oh group which can form hydrogen bonds with water

34
Q

What is a target molecule

A

used to des cirbe the compound that the chemist is attempting to prepare by organic synthesis

35
Q

How do you convert a starting molecule in a target molecule

A
  • identify the functional groups in your starting and target molecule
  • identify the intermediate that links the starting and the target molecules
  • state reagents and conditions in each step