alcohol Flashcards

1
Q

How can alkenes be made sustainably

A

Through fermentation of glucose from

plants

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2
Q

What is the process that alkenes are made from alcohol

A

dehydration

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3
Q

what is a non renewable way of making alkenes from alcohols

A

from crude oils

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4
Q

what are alkenes used to be make

A

polymers- made into plastic

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5
Q

What does a dehydration of alcohol reaction require

A

acid catalyst- H2SO4 ( sulfuric acid) or phosphoric acid H3PO4

normal equation: C2H5OH -> C2H4 + H2O
ethanol-> ethene + water

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6
Q

what is the mechanism for dehydration of alcohols

A

Elimination mechanism

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7
Q

making cyclohexene step 1

A

add conc sulfuric acid, phosphoric acid and cyclohexane’s into round bottomed flask, add several anti bumping granules to allow a smooth boiling process

use heating mantle to warm reactants to 83°c ( boiling point of cyclohexanol) - we don’t use bunsen burner because cyclohexanol is flammable

chemicals w boiling points lower than 83°c will evaporate and enter the condenser , cool down and condense back into a liquid, the condenser has cold running water running through the wall

product is collected in vessel e.g clinical flask, however product will have small amounts of impurities such as unreavyer cyclohexanol and water

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8
Q

Making cyclohexene step 2

A

Separation and purification
add products from step 1 into a separating funnel, add water to dissolve soluble impurities to create a aqueous solution

After allowing the solution to settl, 2 layers will form
Top layer- impure cyclohexene
Bottom layer- aqueous layer containing water soluble impurities
Drain aqueous layer off ( remove stopper)

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9
Q

making cyclohexene step 3

A

Take impure cyclohexene from step 2 and add to round bottomed flask

Add anhydrous CaCl2, this is a dehydrating agent and will remove aq substances still remaining, invert flask and leave it for 20-30 mins

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10
Q

Hydration of alkenes:

What’s produced and what’s needed

A

alcohols are produces
steam and acid catalyst (H+) is needed

we can make ethanol by reacting steam and ethene with a phosphoric acid catalyst, a temp of 300° and 60atm

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11
Q

What is fermentation an alternative to?

A

Ethene and steam when making ethanol

using ethene to make ethanol requires crude oil which isn’t sustainable
using fermentation is renewable as it uses glucose from plants

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12
Q

What does fermentation use and in what conditions

A

yeast in aerobic conditions

- reaction is exothermic

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13
Q

What’s the fermentation reaction

A

C6H12O6 (aq) -> 2C2H5OH (aq) + 2CO (g)

glucose -> ethanol + Carbon dioxide

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14
Q

What is yeast and what does it do

A

it’s an enzyme and it converts glucose into CO2 and ethanol

30-40 optimum temp

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15
Q

fermentation advantages

A

Requires little equipment and uses renewable energy sources so it’s cheap
Biggest cost however is fractional distillation which requires energy and time ( to purify ethanol after fermentation )

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16
Q

What is ethanol and what is it made of

A

it’s a biofuel and is made of dead biological matter

17
Q

advantage of biofuel

A
  • renewable ( more sustainable than crude oil)

- produce CO2 when burnt however they are carbon neutral as CO2 is absorbed by sugar cane when it’s growing

18
Q

disadvantage of biofuel

A

expensive to convert existing petrol engines to take fuels with high conc of ethanol

land used to grow food is being used to make fuel, could cause food shortages in countries that grow sugar cane like brazil

19
Q

To produce an aldehyde what reaction is it carried out in

A

distillation

aldehyde gas condenses into flask

20
Q

What reaction is carried out to produce carboxylic acid

A

reflux
reflux condenser condenses gases and forces them back into reaction vessel, putting the aldehyde back in the flask to be oxidised again

21
Q

Fehlings solution

A

when u add to aldehyde Cu2+ oxidises aldehyde and is reduced to Cu+

Aldehyde goes from deep blue to brick red precipitate
ketone no colour change

22
Q

How to tell a tertiary alcohol from a secondary

A

Use acidified potassium dichromate
tertiary alcohol will not change
secondary will change from orange to green

23
Q

tollens reagent

A

aldehyde turns silver solid/ mirror

ketone does not react

24
Q

how to tell an alkene from an alkane

A

add bromine water and shake
alkane- no colour change - stays orange
alkene- goes from orange to colourless

25
Q

why is the c-o-h angle 104.5

A

the two line pairs repel eachother more than the pairs of electrons in a covalent bond