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B3.6 - Organic synthesis

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

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#1
Front (Question)

Draw a diagram of the set up for refluxing reactions.

Back (Answer)

water out at top water out at bottom condenser flask reaction mixture anti-bumping granules upwards arrow heat (bunsen) VERTICAL

#2
Front (Question)

What is the role of anti-bumping granules?

Back (Answer)

Anti-bumping granules are added to the flask to prevent violent boiling

#3
Front (Question)

What is the role of the condeser?

Back (Answer)

The condenser has cold water flowing through it, which condenses evaporated organic vapours back into liquid, returning them to the reaction in the flask

#4
Front (Question)

What does refluxing allow?

Back (Answer)

process allows the organic substances to be heated to their boiling point, speeding up the reaction, without losing material

#5
Front (Question)

Draw a diagram of the set up for distillation.

Back (Answer)

thermometer water out at top water in at bottom condenser round bottomed flask filled with reaction mixture anti-bumping granules upwards arrow heat (bunsen) conical flask - filled with distillate DIAGONAL

#6
Front (Question)

What is the role of the thermometer during distillation?

Back (Answer)

A thermometer is used to monitor the boiling point of the distilling vapour - helps to identify the substance evaporating

#7
Front (Question)

Techniques to purify an organic liquid: 1 redistillation

Back (Answer)

Repeated distillation helps to separate the pure volatile liquid product from impurities with different boiling points The pure product distils over at its characteristic boiling point, leaving impurities behind

#8
Front (Question)

Techniques to purify an organic liquid: 2 extraction

Back (Answer)

When water is added to a mixture of the organic liquid and an organic solvent in a separating funnel, two immiscible layers form The organic liquid product dissolves in the organic layer, while water-soluble impurities dissolve in the aqueous layer The layers are then drained off separately from the tap at the bottom of the funnel

#9
Front (Question)

Techniques to purify an organic liquid: 3 drying

Back (Answer)

Traces of water dissolved in organic products can be removed using drying agents

#10
Front (Question)

What are examples of drying agents - for drying organic compounds?

Back (Answer)

anhydrous magnesium sulphate anhydrous calcium chloride

#11
Front (Question)

Techniques to purify an organic liquid: 4 filtration

Back (Answer)

After drying, the solid drying agent is removed by filtering the mixture, leaving behind the dry purified organic product

#12
Front (Question)

What does a synthetic route outline?

Back (Answer)

outlines the sequence of reactions needed to transform starting materials into the desired end product

#13
Front (Question)

What does a synthetic route detail?

Back (Answer)

• Every chemical intermediate formed along the way • The specific reagents and conditions required at each stage of the process

#14
Front (Question)

Alkane –> halogenoalkane: reagent + condition + reaction type

Back (Answer)

reagent - halogen condition - UV reaction type - free radical substitution

#15
Front (Question)

Alkene –> alkane: reagent + condition + reaction type

Back (Answer)

reagent - H2 condition - Ni catalyst, 150 degrees C reaction type - electrophilic addition

#16
Front (Question)

Alkene –> halogenoalkane: reagent + reaction type

Back (Answer)

reagent - hydrogen halide or halogen reaction type - electrophilic addition

#17
Front (Question)

Halogenoalkane –> alcohol: reagent + condition + reaction type

Back (Answer)

reagent - NaOH(aq) condition - reflux reaction type - nucleophilic substitution

#18
Front (Question)

alcohol –> halogenoalkane: reagent + condition + reaction type

Back (Answer)

reagent - sodium halide, H2SO4 condition - reflux reaction type - nucleophilic substitution

#19
Front (Question)

alkene –> alcohol: reagent + condition + reaction type

Back (Answer)

reagent - steam condition - H3PO4 catalyst, 300 degrees C, 60 atm/reflux reaction type - electrophilic substitution

#20
Front (Question)

alcohol –> alkene: condition + reaction type

Back (Answer)

condition - conc. H2SO4, heat/reflux reaction type - elimination

#21
Front (Question)

alcohol –> carboxylic acid/ketone: reagent + condition + reaction type

Back (Answer)

reagent - K2Cr2O7(aq) condition - H2SO4 catalyst, reflux reaction type - oxidation

#22
Front (Question)

alcohol –> aldehyde: reagent + condition + reaction type

Back (Answer)

reagent - K2Cr2O7(aq) condition - H2SO4 catalyst, distill reaction type - oxidation

#23
Front (Question)

Properties and typical reactions of alkanes

Back (Answer)

non-polar, unreactive free radical substitution

#24
Front (Question)

Properties and typical reactions of alkenes

Back (Answer)

non-polar, electron-rich electrophilic addition