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Elimination Reactions

Elimination removes H and a leaving group from neighboring carbons to make a C=C bond. You will learn E2 and E1, predict Zaitsev versus Hofmann products, use anti-periplanar geometry, and decide when elimination beats substitution.

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What this chapter covers

Key points to know

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What is the rate law for an E2 reaction?

  1. rate = k[R–X]
  2. rate = k[R–X][base]
  3. rate = k[base]
  4. rate = k[R–X]²
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B. E2 is bimolecular: the base and the substrate both take part in the single rate-determining step, so the rate depends on both concentrations.

Common questions

What does this chapter cover?

Elimination Reactions covers The E2 Mechanism & Anti-Periplanar Geometry, Zaitsev vs Hofmann Products, The E1 Mechanism & Alcohol Dehydration, Substitution vs Elimination.

What should I know first?

E2: one step, rate = k[R–X][base] Needs a strong base; reactivity 3° > 2° > 1° Zaitsev: the more substituted alkene is major (small base, E1)

21 original practice questions accompany this chapter in the app. Spaced review brings missed ideas back at the right time; it helps memory but cannot promise you will not miss an idea again.