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Alcohols

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Total cards: 20•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (20)

#1
Front (Question)

What are the conditions for the direct hydration of ethene?

Back (Answer)

Conc. phosphoric acid catalyst 300*C 6000kPa

#2
Front (Question)

Direct hydration of ethene produces a low yield. How can you increase the yield?

Back (Answer)

Recycling unreacted ethene several times

#3
Front (Question)

What are the raw materials needed for the direct hydration of ethene?

Back (Answer)

Ethene (from crude oil)

#4
Front (Question)

What are the conditions for the industrial fermentation of ethene?

Back (Answer)

Enzymes produced by yeast 25-40*C Absence of oxygen

#5
Front (Question)

What is an advantage and disadvantage of using industrial fermentation rather than direct hydration to produce ethanol?

Back (Answer)

Advantages - Utilises renewable resources Cheaper equipment Lower temp and pressure Disadvantages- Lower rate of reaction Not continuous process

#6
Front (Question)

What are biofuels?

Back (Answer)

The fuels made from a renewable biological source

#7
Front (Question)

If you partially oxidise a primary alcohol what is produced?

Back (Answer)

An aldehyde

#8
Front (Question)

If you fully oxidise a primary alcohol what is produced?

Back (Answer)

A carboxylic acid

#9
Front (Question)

How do you get an aldehyde from a primary alcohol?

Back (Answer)

Partially oxidise. If you use an excess of alcohol and distil off the aldehyde as soon as it forms. Separates from oxidising agent

#10
Front (Question)

How do you get a carboxylic acid from a primary alcohol?

Back (Answer)

Fully oxidise Alcohol heated under reflux with an excess of the oxidising agent Carboxylic acid distilled off once the reaction is complete

#11
Front (Question)

Why, when making in aldehydes, is the product distilled off as soon as it forms?

Back (Answer)

To remove it from the oxidising agent to prevent it from being oxidised further into a carboxylic acid

#12
Front (Question)

How are alcohols produced industrially?

Back (Answer)

The hydration of alkenes in the presence of an acid catalyst

#13
Front (Question)

What is the name of the reaction whereby alcohols are converted to alkenes?

Back (Answer)

Elimination reaction

#14
Front (Question)

What is a suitable catalyst for the elimination reaction of alcohols to produce alkenes?

Back (Answer)

Hot concentrated sulphuric acid

#15
Front (Question)

What can the product of an elimination reaction of alcohols be used for?

Back (Answer)

Can supply alkene monomers for polymerisation from a renewable raw material

#16
Front (Question)

Describe and explain the simple acid-catalysed elimination mechanism with propan-2-ol

Back (Answer)

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#17
Front (Question)

What is a suitable oxidising agent?

Back (Answer)

Acidified potassium dichromate (VI)

#18
Front (Question)

What are secondary alcohols oxidised to?

Back (Answer)

Ketones

#19
Front (Question)

Describe and explain the simple acid-catalysed hydration mechanism with ethene

Back (Answer)

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#20
Front (Question)

Describe and explain the production of ethanol from the nucleophilic substitution of bromoethane

Back (Answer)

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