Answer
Flashcards · 7405 · A Level Topic 32
Organic synthesis (A Level) flashcards
7 cards on A Level Topic 32. Pick a subtopic or study them all.
Study mode needs JavaScript. Every card is listed below, so you can still cover the answers and test yourself.
Choose your cards
Session complete
Worth another look:
All 7 cards
For a quick read-through or printing. Cover the right-hand side to test yourself.
Topic 32: Organic synthesis
- Percentage atom economy
- (Mr of the desired product ÷ sum of Mr of all reactants) × 100.
- Why do chemists aim for processes that need no solvent?
- Solvents must be made, transported and separated from the product (often by energy-intensive distillation), become waste unless recycled, and are often flammable or toxic.
- Why do chemists aim for fewer steps?
- Product is lost at every step, so the overall yield falls; each step also needs its own reagents, separation, energy and time.
- Overall yield of a three-step route with step yields 80%, 70% and 50%
- 0.80 × 0.70 × 0.50 = 0.28, so 28%. Multiply the yields; never add or average them.
- Which reactions in the course make a new C–C bond?
- KCN with a halogenoalkane; KCN with an aldehyde or ketone; Friedel–Crafts acylation (and addition polymerisation).
- Atom economy of an addition reaction
- Exactly 100%: there is only one product. Substitution and elimination are always below 100%.
- Route: 1-bromopropane to butylamine
- KCN in aqueous ethanol, reflux → butanenitrile; then reduce (e.g. LiAlH₄, or H₂ with Ni) → butylamine.