Chemistry- organic synthesis Flashcards

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1
Q

what is reflux

A

technique used to heat volatile liquids

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2
Q

how does reflux work

A

strongly heated without losing volatile reactants and products. Volatile compounds evaporate and condense -falls back into the flask

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3
Q

what does volatile mean

A

how easily a substance will vaporize

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4
Q

how does a liebig condenser work

A

cold water running through wall, hot evaporating substances turn back into a liquid and return back to round bottomed flask.

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5
Q

how do we need to be careful when using flammable liquids

A

use water bath or electric heater: mantle

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6
Q

what is distillation

A

used to separate substances with different boiling points

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7
Q

how does distillation work

A

gently heating mixture will result in the compounds separating out in order of boiling point. knowing the boiling point of the chemical will allow you to decide how to separate the compound

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8
Q

what will happen if the compound has lower boiling point than starting mixture

A

heat to the temp of boiling point of the compound

collect product in a separate vessel

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9
Q

what will happen if the compound has higher boiling point than starting mixture

A

heat to temp of boiling temp of compound

product will remain on the round bottomed flask

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10
Q

what is distillation useful for

A

useful when you want to extract a chemical before it reacts any further.

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11
Q

example of distillation

A

oxidising primary alcohols can produce aldehydes however if aldehyde isn’t removed as soon as its formed it will oxidise to form a carboxylic acid

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12
Q

what is filteration

A

used to separate solids and liquids

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13
Q

what does the vacuum do

A

used to help separate liquid and solid components thoroughly.
vacuum creates reduced pressure in flask and pulls liquid through
Solid is left in the buchner funnel

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14
Q

how do we purify this further?

after distillation

A

recrystallisation

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15
Q

what is recrystallisation

A

method to purify solids

-solvent chosen is very important

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16
Q

steps for recrystallisation

A
  1. add enough solvent, impure solid dissolves
  2. cool the solution down slowly, crystals will start to form
  3. impurities will remain dissolved in solution takes longer for them to crystallise
  4. filter collects purified crystals, wash in cold solvent to dry of
17
Q

why do we choose the solvent carefully

A

want impure solid to dissolve fully in hot solvent but be insoluble when its cold. if substance doesn’t dissolve in hot solvent, cant be purified further

18
Q

what does measuring boiling point detect

A

detects impurities

19
Q

how to carry out distillation to determine boiling point

A

1- gently heat sample, can then measure temperature at which it distils using thermometer
2.then compare this boiling point with data book value

20
Q

how do we know if sample contains impurities

A
  • if boiling point is higher than what is in data book

- sample boils over a range of temperatues

21
Q

what is needed to be done if compounds have same boiling points

A

need to use analytical techniques such as mass spectrometry to spot impurities

22
Q

how can purity of a compound be measured

A

can be determined by measuring the melting point

23
Q

how to carry out purification

A
  1. add sample of solid into capillary tube and place into heating element
  2. slowly increase temperature until substance starts to melt
  3. temperature ranges from when it begins to melt to when it fully melts
  4. compare melting points (using data book values)
  5. if substance contains impurities the melting point will be lower and temp range substance melts at will be higher
24
Q

alkanes

A

properties: unreactive, non-polar bond
Reactions: radical substitution

25
Q

alkene

A

properties: non-polar bond
reactions: electrophilic addition

26
Q

aromatic compounds

A

properties: delocalised ring
reaction: electrophilic substitution

27
Q

alcohols

A

properties: lone pair on oxygen turns into nucleophile, polar C-OH bond
reactions:
- esterification + nucleophilic substitution

28
Q

haloalkane

A

properties: polar c-x bond
reactions: nucleophilic substitution + elimination

29
Q

what are the 7 different reaction types

A
  • addition reaction
  • substitution reaction
  • elimination/dehydration
  • condensation reaction
  • hydrolysis
  • oxidation
  • reduction
30
Q

addition reaction

A

double bond is broken, 2 molecules join together to form single product
functional groups involved: alkene, ketone, aldehydes

31
Q

substitution reactions

A

functional group is exchanged for another one

functional groups: halogens, benzene, alcohol

32
Q

elimination-dehydration

A

double bond is formed when a functional group is removed and released as part of a smaller molecule

33
Q

condensation reaction

A

when two molecules join and small molecule is eliminated

carboxylic acid, amide, alcohol, acid chlorines

34
Q

hydrolysis

A

2 smaller molecules formed by splitting lager one with water (breaking polyamides and polyesters)

35
Q

oxidation

A

loss of electrons

1) primary alcohol to aldehydes to carboxylic acid
2) secondary alcohol to ketone

36
Q

reduction

A

gain of electrons

primary alcohol to aldehydes to carboxylic acid