Back to marketplace

ORGANIC CHEM - ALCOHOLS

No description yet. This curated deck is ready for daily study.

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

Card preview (20)

#1
Front (Question)

How are alcohols produced?

Back (Answer)

hydration of alkenes with an acid catalyst (electrophilic addition)

#2
Front (Question)

How can ethanol be produced?

Back (Answer)

• hydration of ethene in the presence of an acid catalyst • fermentation

#3
Front (Question)

What is the equation for fermentation?

Back (Answer)

C6H12O6 -> 2C2H5OH + 2CO2

#4
Front (Question)

What is a biofuel?

Back (Answer)

a fuel derived from living matter (eg: ethanol produced from the fermentation of glucose)

#5
Front (Question)

What does carbon neutral mean?

Back (Answer)

no net emissions of CO2 to the atmosphere

#6
Front (Question)

Why is bioethanol being used as a fuel considered carbon neutral?

Back (Answer)

the amount of CO2 released when it’s burned is the same amount of CO2 that is absorbed by plants for photosynthesis

#7
Front (Question)

Why is the claim that bioethanol is carbon neutral incorrect?

Back (Answer)

doesn’t take into account CO2 released from other things like transporting the bioethanol

#8
Front (Question)

What is a primary alcohol?

Back (Answer)

C atom bonded to the hydroxyl (-OH) group is attached to only one other C atom

#9
Front (Question)

What is a secondary alcohol?

Back (Answer)

C bonded to the hydroxyl (-OH) group is attached to 2 other C atoms

#10
Front (Question)

What is a tertiary alcohol?

Back (Answer)

C bonded to the hydroxyl (-OH) group is attached to 3 other C atoms

#11
Front (Question)

Elimination by dehydration of an alcohol: - reagent? - conditions? - what happens?

Back (Answer)

• reagent: H2SO4 • conditions: hot, conc. H2SO4, 180°C • alcohol is dehydrated (loses H2O) to form an alkene

#12
Front (Question)

What is used to oxidise alcohols?

Back (Answer)

acidified potassium dichromate (K2Cr2O7 + H2SO4)

#13
Front (Question)

Primary alcohol + [O] -> ?

Back (Answer)

aldehyde + H2O

#14
Front (Question)

Aldehyde + [O] -> ?

Back (Answer)

carboxylic acid

#15
Front (Question)

Primary alcohol + 2[O] -> ?

Back (Answer)

carboxylic acid + H2O

#16
Front (Question)

Secondary alcohol + [O] -> ?

Back (Answer)

ketone + H2O

#17
Front (Question)

What is used to convert primary alcohols to aldehydes?

Back (Answer)

distillation

#18
Front (Question)

What is used to convert primary alcohols to carboxylic acids?

Back (Answer)

reflux

#19
Front (Question)

Things to include in a distillation diagram

Back (Answer)

• round-bottomed/pear shaped flask • bung and thermometer at the top of the flask • acidified potassium dichromate • heat source • condenser going into a conical flask • water going in at the bottom of the condenser and out at the top

#20
Front (Question)

Things to include in a reflux diagram

Back (Answer)

• round-bottomed/pear shaped flask • acidified potassium dichromate • heat source • vertical condenser which should be open at the top • water going in at the bottom of the condenser and out at the top