6E -ALCOHOLS Flashcards

1
Q

general formula for alcohols? (1)

A
  • CnH2n+1OH
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2
Q

what 3 types of alcohols can you get and how ?

3

A
  • primary alcohol =OH attached to carbon with 1 other C attached ( 1 r group)
  • Secondary alcohol = OH attached to carbon attached to 2 Carbons ( 2 r groups )
  • Tertiary alcohol=OH attached to Carbon (with 3 r groups)
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3
Q

Alcohol +Oxygen (combustion )

A

-CO2 +H2O

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4
Q

Alcohol+PCl5 or HCl ? produces?
which type of alcohol is fastest ?
(3)

A
  • CHLOROALKANE
  • nucleophilic substitution
  • fastest with tertiary alcohol (sn1 mechanism favoured)
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5
Q

how do you make bromoalkanes ?(3)

A
  • Bromoalkane
  • ALCOHOL + 50% CONC sulphuric acid +KBr
  • ACID CATALYST
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6
Q

how do you make iodoalkanes ?(3)

A
  • red phosphorous and iodine
    -reflux alcohol with red phosphorus and iodine to produce insitu PI3
    General Equation : 3ROH + PI3 —>3RI +H3PO3
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7
Q

How can you form an Alkene from an Alcohol ?

4

A
  • DEHYDRATION REACTION (elimination where water is eliminated )
  • Alcohol + Acid Catalyst such as CONCENTRATED phosporic acid (H3PO4)
  • heated !
  • water is eliminated
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8
Q

what will primary alcohols oxidise to ? (1)

A
  • aldehydes –> carboxylic acids
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9
Q

what will secondary alcohols oxidise to ? (1)

A

-KETONES

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10
Q

what will tertiary alcohols oxidise to ? (1)

A
  • They WON’T
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11
Q

what is the general formula for an Aldehyde or Ketone ?

1

A

-CnH2nO

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12
Q

What is an aldehyde? (1)

A
  • one alkyl group attached to carbonyl carbon atom C=O
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13
Q

what is a ketone ? (1)

A

-have two alkyl groups attached to carbonyl carbon atom

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14
Q

How can you test for Aldehydes and ketones?

4

A
  • Benedicts solution = cu2+ dissolved in sodium carbonate
    =aldehyde = turn from blue to brick red ppt
    cu2+ ions reduced
    -Fehling’s solution :
    =blue to red in aldehydes
    =contains cu2+ dissolved in sodium Hydroxide
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15
Q

how can you make a aldehyde from a Primary alcohol ?

5

A
  • OXIDISE WITH POTASSIUM DICHROMATE
  • distill to get Aldehyde
  • gently heating excess alcohol with controlled amount o Potassium Dichromate
  • distillation apparatus
  • so aldehyde which boils at lower temp is distilled of immediately .

or you could gently heat with alcohol with potassium dichromate and H2SO4 in test tube –> aldehyde –>carboxylic acid

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16
Q

how can you make a carboxylic acid from a primary alcohol ?

2

A
  • vigourous OXIDATION WITH POTASSIUM DICHROMATE

- REFLUX

17
Q

How can you make ketones ?(2)

A
  • acidified Potassium DICHROMATE

- REFLUX

18
Q

how can you oxidise tertiary alcohols ?(1)

A
  • Burn them
19
Q

why do we reflux? (2)

A
  • condenses vapours giving the substance time to react

- also makes sure you down lose any volatile substances .

20
Q

why do we carry out distillation? (1)

A
  • separate products based on bp
21
Q

how do we determine impurities ? (2)

A
  • Boiling points- thermometer on distillation

- if the value is higher than data book value = IMPURITIES!

22
Q

How do we remove traces of water ?

2

A
  • add drying agent = ANHYDROUS SALT i.e. : MgSO4 BINDS TO WATER = HYDRATED and takes away water !
  • filter away after
23
Q

How do we make Alkenes from alcohols ?

2

A
  • dehydration reaction

- heat with strong acid such as h2so4 or phosphoric acid