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Alcohols

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What is the functional group for alcohols

Back (Answer)

-OH Hydroxyl group

#2
Front (Question)

What is a primary alcohol

Back (Answer)

An alcohol with 1 alkyl group attached to the same carbon which the -OH is attached to

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#3
Front (Question)

What is a secondary alcohol

Back (Answer)

An alcohol with 2 alkyl groups attached to the same carbon which the -OH is attached to

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#4
Front (Question)

What is a tertiary alcohol

Back (Answer)

An alcohol with 3 alkyl groups attached to the same carbon which the -OH is attached to

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#5
Front (Question)

How can we sustainably make an alkene from an alcohol

Back (Answer)

Dehydrate an alcohol which is produced via the fermentation of glucose from plants in the presence of an acid catalyst

#6
Front (Question)

What do we call the process of eliminating water from a molecule

Back (Answer)

Dehydration

#7
Front (Question)

What is the benefit of dehydrating an alcohol which is produced via the fermentation of glucose from plants to produce an alkene rather than extracting them from crude oil

Back (Answer)

Crude oil is non-renewable therefore this process is not sustainable. Plants are renewable and so that process is sustainable

#8
Front (Question)

How can we form an alcohol from an alkene

Back (Answer)

Hydrate the alkene in the presence of an acid catalyst

#9
Front (Question)

Give an equation for the dehydration of ethanol to produce an alkene

Back (Answer)

Must be done in warm conditions (under reflux) and in the presence of concentrated sulfuric acid

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#10
Front (Question)

What is the mechanism by which the dehydration of alcohols to form an alkene occurs

Back (Answer)

Acid catalysed elimination

#11
Front (Question)

What can alkenes which are produced by the dehydration of alcohols be used for. What is the benefit of this over an alternative method

Back (Answer)

Used to produce addition polymers without using monomers derived from crude oil.

#12
Front (Question)

Outline the mechanism for the formation of ethene via the dehydration of ethanol

Back (Answer)

Elimination

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#13
Front (Question)

What can occur when we dehydrate secondary or tertiary alcohols to form an alkene

Back (Answer)

May form 2 different alkenes due to the ability for the double bond to occur on either side of the OH group

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#14
Front (Question)

When we dehydrate an alcohol, the mixture is impure. What are the components of this impure mixture

Back (Answer)

Alkene Alcohol Water Acid

#15
Front (Question)

How can we separate an impure mixture produced from the dehydration of an alcohol

Back (Answer)

Distillation

#16
Front (Question)

What is distillation

Back (Answer)

The separation of chemicals by boiling point

#17
Front (Question)

What can we do to further purify an impure mixture produced from the dehydration of an alcohol which has already been distilled

Back (Answer)

We can use a separation funnel to separate aqueous and organic layers The addition of a drying agent ( to remove any H2O)

#18
Front (Question)

What is the desired product from the dehydration of an alcohol

Back (Answer)

A pure alkene

#19
Front (Question)

What are the 3 steps in producing cyclohexene from an alcohol

Back (Answer)

Distillation Separation Purification

#20
Front (Question)

What alcohol is cyclohexene produced from

Back (Answer)

cyclohexanol

#21
Front (Question)

What is the reagent and conditions required for the dehydration of an alcohol to form an alkene, and what is the name of the mechanism

Back (Answer)

Elimination Reagent: Hot Concentrated sulfuric acid Conditions:180 degrees C (under reflux),

#22
Front (Question)

Outline step 1 in the production of cyclohexene from cyclohexanol

Back (Answer)

Step 1: Distillation: • Add concentrated sulfuric acid and cyclohexanol to a round bottomed flask. • Add several anti-bumping granules to allow for a smooth boiling process • Use a heating mantle to warm the reactants up to 83C (B.P of cyclohexanol) • Chemicals with B.P less than 83C will evaporate, enter the condenser ,cool down and condense back into a liquid • Product is then collected in a conical flask, yet this product will still have small amounts of impurities such as unreacted cyclohexanol and water

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#23
Front (Question)

What is the purpose of adding anti bumping granules during distillation

Back (Answer)

Allows for a smooth boiling process by preventing large bubbles from forming

#24
Front (Question)

What is the boiling point of cyclohexanol

Back (Answer)

83 degrees C