Synthetic Routes (OCR A-Level Chemistry A): Flashcards

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Synthetic routes
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Organic synthesis

Building complex molecules from simpler starting materials

Functional group

Reactive part of molecule determining its chemical properties

Central role of alcohols in synthesis

Can be converted to many other functional groups

1° alcohol → aldehyde: conditions

\ceK2Cr2O7/H2SO4\ce{K2Cr2O7/H2SO4}, distil

1° alcohol → carboxylic acid: conditions

\ceK2Cr2O7/H2SO4\ce{K2Cr2O7/H2SO4}, reflux

2° alcohol → ketone: conditions

\ceK2Cr2O7/H2SO4\ce{K2Cr2O7/H2SO4}, reflux

Target molecule

Compound you're trying to make through organic synthesis

Intermediate (in synthesis)

Stepping stone molecule between start and target

Ozonolysis

Breaks \ceC=C\ce{C=C} bonds to form aldehydes/ketones

Why distil when making aldehyde from 1° alcohol

Prevents further oxidation to carboxylic acid

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