Back to marketplace

alcohols

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

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

Card preview (24)

#1
Front (Question)

what is the general formula for alcohols?

Back (Answer)

Cn H2n+2 O

#2
Front (Question)

what is the functional group of alcohols?

Back (Answer)

R-OH

#3
Front (Question)

what can we classify alcohols as?

Back (Answer)

primary secondary or tertiary

#4
Front (Question)

what are functional group isomers of alcohols?

Back (Answer)

ethers (hydrogen from R-OH replaced with another R group)

#5
Front (Question)

what is hydrolysis?

Back (Answer)

breaking a bond using water

#6
Front (Question)

what are the three mechanisms of making alcohols?

Back (Answer)

-hydrolysis of organic hydrogensulfates -nucleophilic substitution -electrophilic addition (steam hydration of ethene)

#7
Front (Question)

how do we get alcohols from organic hydrogensulfates?

Back (Answer)

they are easily hydrolysed so hydrolyse using warm water to form alcohols

#8
Front (Question)

what is regenerated at the end of hydrolysis of organic hydrogensulfates and what does this act as?

Back (Answer)

sulfuric acid (H2SO4) so it acts as a catalyst

#9
Front (Question)

what are the 3 uses of alcohols?

Back (Answer)

-alcoholic drinks -solvents -chemical feedstock (used to make other chemicals)

#10
Front (Question)

what kind of boiling points do alcohols usually have and why?

Back (Answer)

high because they form hydrogen bonds with each other

#11
Front (Question)

why are only some alcohols soluble?

Back (Answer)

ones with a lower Mr are soluble in water because they can form hydrogen bonds with water

#12
Front (Question)

what are the conditions for making an alcohol via nucleophilic substitution?

Back (Answer)

aqueous sodium hydroxide, warm

#13
Front (Question)

what reaction is used in industry to produce ethanol and what mechanism does it use?

Back (Answer)

steam hydration (addition of water) of ethene electrophilic addition

#14
Front (Question)

what are the conditions for steam hydration of ethene?

Back (Answer)

steam (300 degrees), pressure of 60atm and phosphoric acid catalyst (H3PO4)

#15
Front (Question)

what type of reaction is steam hydration of ethene and what does this mean for the yield?

Back (Answer)

it is reversible and the yield is very low

#16
Front (Question)

how is yield improved by steam hydration of ethene?

Back (Answer)

any unreacted ethene gas can be recycled and increases the overall yield

#17
Front (Question)

what are some advantages of using steam hydration of ethene?

Back (Answer)

-product is pure (No waste product including CO2) -we can manipulate the reversible reaction to increase yield -higher temperature, therefore, fast rate of reaction -can recycle unused reactants such as ethene gas.

#18
Front (Question)

what are some disadvantages of steam hydration of ethene?

Back (Answer)

-reversible reaction so not 100% yield -ethene is from crude oil contributing to environmental pollution. Thermal cracking of crude oil requires energy. -higher temps required so higher energy consumption

#19
Front (Question)

what is the alternative industrial method for making alcohols that doesn’t use a mechanism?

Back (Answer)

fermentation

#20
Front (Question)

what are the reagents of fermentation?

Back (Answer)

yeast and glucose (C6H1206)

#21
Front (Question)

what are the conditions for fermentation?

Back (Answer)

30-40 degrees, aqueous, anaerobic

#22
Front (Question)

what is the role of yeast in fermentation?

Back (Answer)

catalyst

#23
Front (Question)

why is it important that fermentation occurs in anaerobic conditions?

Back (Answer)

yeast won’t ferment in oxygen and oxyegn would cause the ethanol to be oxidised to ethanal

#24
Front (Question)

why do we use 30-40 degree temperatures for fermentation?

Back (Answer)

compromise because too high temp causes yeast to denature and not ferment