Alcohols Flashcards

1
Q

Primary, secondary, tertiary alcohol

A

1° - carbon carrying -OH only attached to one alkyl group

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2
Q

How can alcohols form alkenes

A

Dehydration reaction- eliminate water
-heated with conc sulfuric acid catalyst
+ allows produce alkene from renewable resource (alcohol from fermentation)
+polymers without oil

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3
Q

How to produce alkene from alcohol

A

Distillation-
-add conc H2SO4 + H3PO4 to round bottom flask containing cyclohexanol, add carborundum boiling chipe, swirl
-gently heat water bath
-chemicals evaporate, into condenser, turn to liquid
-collect in cooled flask
Separation-
-will contain impurities
-separating funnel, add water to dissolve soluble impurities
-allow mixture settle into layers, drain aqueous lower layer, leave impure cyclohexene
Purification-
-drain into round bottom flask
-add anhydrous CaCl2 add bung, leave to dry
-distil ahain

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4
Q

Hydration to form alcohol conditions

A

-react ethane with steam to produce ethanol
-300°C
-60atm
H3PO4 catalyst

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5
Q

Hydration properties

A
  • non renewable
  • continuous process
  • not carbon neutral
  • fast
  • pure product (100%)
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6
Q

Fermentation conditions

A

Sugar from plant material (glucose) converted to ethanol and CO2 by fermentation

  • 35°C (optimum temp for yeast)
  • yeast catalyst
  • atmospheric
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7
Q

Fermentation properties

A
  • renewable- sugar
  • batch process
  • carbon neutral
  • slow
  • impure product (15%): fractional distillation needed
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8
Q

Biofuel

A

A fuel made from biological material that’s recently died

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9
Q

How is fermentation carbon neutral?

A

The CO2 released when the fuel is burnt is equal to the CO2 absorbed by plants

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10
Q

Advantages and drawbacks of biofuels over fossil fuels

A

+renewable (won’t run out) so more sustainable
+carbon neutral
-petrol car engines must be modified to use fuels with high ethanol conc
-less land to grow food (crops take up space) so harder to feed

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11
Q

Equations to support carbon neutral

A
Photosynthesis-
6CO2 + 6H2O —> C6H12O6 + 6O2
Fermentation-
C6H12O6 —> 2C2H5OH + 2CO2
combustion of ethanol-
2C2H5OH + 6O2 —> 4CO2 + 6H2O
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12
Q

How is it not completely carbon neutral?

A

Fossil fuels burnt to power machinery used to make fertiliser, harvesting crops, refine + transport bio ethanol
-produces carbon dioxide

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13
Q

Oxidising agent

A

[o]= acidified potassium dichromate

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14
Q

What are alcohols oxidised to?

A

Primary alcohol - aldehyde - carboxylic acid (p-a= distillation, p-c= reflux)
Secondary alcohol - ketone (reflux)
Tertiary alcohol- not easily oxidised

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15
Q

How can you tell if it’s been oxidised

A

Orange dichromate ion reduced to green chromium ion
Primary + secondary- will change from orange solution to green solution
Tertiary- will remain orange solution

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16
Q

What are aldehydes

A
  • H and one alkyl group attached to carbonyl C atom
    -al
    -C=O
    |
    H
    -C in -CHO group always counted as 1st carbon
17
Q

What are ketones

A
  • 2 alkyl groups attached to carbonyl C atom
  • one
  • C=O in middle of carbon chain
18
Q

What are carboxylic acids

A

-COOH group at end of carbon chain
-oic acid
-C=O
|
O-H
-C in COOH counted as 1st

19
Q

How can aldehydes and ketones be distinguished

A

-Weak oxidising agents can be used to distinguish between an aldehyde and a ketone
The aldehyde will be oxidised to a carboxylic acid, but the ketone will not undergo oxidation
-If an aldehyde is warmed with Fehling’s solution, the aldehyde will be oxidised and a colour change will take place: blue- brick red precipitate
-If gently warmed with Tollens’ reagent, an aldehyde will become oxidised- silver mirror