Organic Chemisty Part 3 Flashcards

1
Q

What are alcohols?

A
-OH functional group
Suffix -ol
General formula Cn H2n+2 O
Very flammable
Unsaturated (all single bonds)
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2
Q

Combustion of ethanol in air (complete combustion)

A

Cobalt chloride paper blue -> pink
Limewater colourless -> cloudy

Ethanol + oxygen -> carbon dioxide + water
C2H6O + 3O2 -> 2CO2 + 3H2O

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3
Q

Reaction of ethanol with oxygen in air

A

Produces vinegar (aqueous solution of ethanoic acid)
Microbial action
Oxidation reaction

Ethanol + oxygen -> ethanoic acid + water
C2H6O + O2 -> CH3COOH + H2O

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4
Q

Reaction when heating acidified potassium dichromate (VI) in ethanol

A

Potassium dichromate solution orange -> green
Smells like vinegar

Dichromate (vi) ion (orange) reduced to chromium (iii) ion (green)
Ethanol oxidised

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5
Q

How can ethanol be manufactured?

A

Hydration of ethene OR fermentation of glucose

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6
Q

Hydration of ethene to produce ethanol

A

C2H4 + H2O -> C2H5OH
Use phosphoric (v) acid as catalyst
Optimum conditions are 300°C and 60-70atm
Efficient as uses continuous flow process, very rapid
Produces very pure ethanol
Uses high temperatures and pressures, needs lots of energy input (crude oil)
Expensive as lots of equipment needed

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7
Q

Fermentation of glucose to produce ethanol

A

C6H12O6 -> 2C2H5OH + 2CO2
Needs sugar in water, yeast as catalyst temperature of 30-40°C, absence of acid
After a few days, process stops as high alc content (up to 14%) kills of yeast
Produces impure ethanol
Slow/inefficient batch process
Gentle temperature and pressure, little energy needed

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8
Q

What are carboxylic acids?

A
Functional group COOH
General formula CnH2nO2
Carbon-carbon double bond
Suffix -oic + acid
Eg ethanoic acid (vinegar)
Weak acids
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9
Q

Reaction of carboxylic acids with metals

A

carboxylic acid + metal -> salt + hydrogen
eg ethanoic acid + sodium -> sodium ethanoate + hydrogen
Test for gas produced using squeaky pop test

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10
Q

Reaction of carboxylic acid with metal carbonates

A

Carboxylic acid + metal carbonate -> salt + water + carbon dioxide

eg ethanoic acid + sodium carbonate -> sodium ethanoate + water + carbon dioxide
eg CH3COOH + Na2CO3 -> 2NaCH3COO + H2O + CO2

Effervescence

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11
Q

What are esters?

A

Functional group COO
Made by reacting an alcohol with a carboxylic acid with sulphuric acid catalyst (condensation polymerisation)
eg ethyl ethanoate (C4H8O2) is ethanol + ethanoic acid
Alcohol prefix +yl, ethanoic acid prefix +oate
Strong fruity smells
Can be used as solvents

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12
Q

What is a polymer?

A

Lots of small molecules joined up

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13
Q

Positives and negatives of polymers

A

They can be strong, flexible and durable

They are hard to dispose of as they are inert and non-biodegradable

Biopolysters are biodegradable

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14
Q

Disposal of polymers by incineration

A

The heat produced can be used as an energy source

Carbon dioxide and other toxic gases are produced, contributing to global warming

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15
Q

Disposal of polymers by recycling

A

Reduces the amount of crude oil used, no toxic gases produced

Requires sorting, melting and reforming polymers can be expensive and difficult

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16
Q

Condensation polymerisation

A

Reaction between monomers with functional groups at both ends, produces polymer and water molecule
eg polyester
dicarboxylic acid + diol -> polyester + water