chemistry 2.2 Flashcards

1
Q

What are the two chemical processes by which ethanol can be made?

A

Fermentation of sugars

Hydration of ethene

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2
Q

How is ethanol manufactured by the hydration of ethene ?

A
  • Using steam in the presence of a phosphoric acid catalyst
  • carried out at 300 degrees and 60 atm
  • reversible so incomplete…95% conversion rate
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3
Q

How is fermentation used to make ethanol?

A
  • Starch or sugar converted into ethanol and CO2
  • catalyst in yeast called zymase
  • done at 37degrees
  • above 37 the enzyme is denatured
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4
Q

What limits the conversion of sugars to ethanol

A

Toxicity of alcohol as above 14% denatures enzyme

Done in the absence of air as anaerobic

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5
Q

Give some uses of ethanol other than alcohol

A
  • perfume
  • methylated spirits
  • mixed with petroleum as fuel
  • cleaning fluids
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6
Q

How are spirits made from ethanol?

A
  • heated alcohol-water mixture to distill
  • alcohol boils off faster than water and is moved to be condensed
  • distillate higher alcohol content than liquid
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7
Q

What are methylated spirits used for and how are they made?

A
  • fuel in spirit burners and camping stoves
  • removing paint or ink stains
  • made by adding methanol to ethanol and dye; makes it toxic and undrinkable
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8
Q

Defined volatility

A

The ease for a liquid to turn into a gas which increases with a smaller boiling point

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9
Q

Why do alcohols dissolve in water?

A

Because hydrogen bonds form between the polar OH groups of the alcohol and water molecules

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10
Q

Why does solubility decrease as the chain length increases

A

A larger part of the alchohol molecule is made up of a non polar hydrocarbon chain
Hydrocarbon chain does not form hbonds with water molecules

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11
Q

How would you classify a primary alcohol
How would you classify a secondary alcohol
How would you classify a tertiary alcohol

A
  • OH group is attached to a carbon atom with no or one alkyl group
  • OH group is attached to a carbon with 2 alkly groups
  • OH group attached to a carbon bonded to 3 alkyl groups
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12
Q

What is a suitable oxidising agent and how can it be made

A
  • a solution with acidified dichromate ions

- made by mixing potassium dichromate and sulfuric acid

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13
Q

What do primary alcohols oxidise to

A

gentle heating = aldehyde

stronger heating = carboxylic acid

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14
Q

Define reflux

A

continual boiling and condensing of a reaction mixture to make sure the flask does not boil dry while the reaction is taking place

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15
Q

What do secondary alchohols oxidise to form

A

ketones

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16
Q

What colour does acidified dichromate change to when successfully oxidised

A

orange to green

17
Q

Define esterification

A

the reaction of an alchohol with a carboxylic acid to form and ester and water

18
Q

How would you prepare an ester

A
  • Put 1cm3 of an alchohol and 1cm3 of a carboxylic acid in a boiling tube and add a few drops of H2SO4
  • put the boiling tube in water bath of 80 degrees for 5 minutes
  • when done put the boiling tube in a cold water bath and the oil that floats on top is the ester
19
Q

Define dehydration

A

an elimination reaction where a water molecule is removed from a saturated molecule to make a unsaturated molecule

20
Q

What are some uses of halogenoalkanes

A

organic sythesis
used to prepare many useful materials
aerosol cans

21
Q

Why do halogenoalkanes contain a polar carbon-halogen bond

A
  • because they have different electronegativities
  • the carbon atom is less electronegative than the halogen atom so the bonded pair is more attracted to the halogen atom
  • this = polar bond
22
Q

Define hydrolysis

A

the reaction of water or aqueous hydroxide to break a chemical compound into two new compounds

23
Q

What do curly arrows respresent

A

the movement of an electron pair

24
Q

LOOK OVER 2.2.6

A

NOW

25
Q

What are the properties of polytetraflouroethane and what can it do

A

strong carbon-fluorine bonds = resistance to chemical attacks
heat resistant
electrical insulator
non stick qualities SO can be used to coat pots and pans or metal surfaces
also used as nail polish

26
Q

What are some uses of PVC

A

drainpipes
plastic window frames
childrens toys
packaging

27
Q

Why were CFC’s first developed

A

refrigerant gases in the 1800’s were fatal when people breathed in the fumes so freon developed CFC’s as an alternative

28
Q

How do CFC’s affect the ozone layer

A

stable until they reach stratosphere where they absorb ultraviolet radiation to form chlorine radicals which break down the ozone

29
Q

What are some alternatives to CFC’s

A

hydroflouroalkanes and hydroflourohydrocarbons

30
Q

how do you work out percentage yield normally and applied to moles

A

actual yield/predicted yield

actual mole/theoretical mole

31
Q

how to work out atom economy

A

molecular mass of desired product/sum of molecular mass of all products

32
Q

what reactions have an atom economy of 100%

A

addition reactions