| English | 意味 |
|---|---|
| halogenoalkane/ˈheɪləʊdʒnəʊlkeɪn/ | ハロゲンアルカン |
| nucleophilic substitution/ˌnjuːklɪəˈfɪlɪk ˌsʌbstɪˈtjuːʃn/ | 求核置換反応 |
| nitrile/ˈnaɪtraɪl/ | ニトリル |
| amine/ˈæmaɪn/ | アミン |
| reflux/ˈriːflʌks/ | 還流 |
Swapping out a halogen
- A halogenoalkane 卤代烷 is an alkane with a halogen in place of hydrogen (a C–X bond).
- The C–X bond is polar, which makes these compounds react.
- They come in three classes.
A halogenoalkane is:
難易度 1/5 · 100 コイン + 今日初回完了時に小ボーナス付与
A halogenoalkane has a polar C–X bond, which is the reactive site.
Halogenoalkanes react with aqueous hydroxide ions by:
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OH⁻ is a nucleophile replacing the halogen.
Three classes
- primary, secondary or tertiary, set by how many carbons are joined to the carbon holding the halogen (one, two or three).
- Made by: free-radical substitution of an alkane, electrophilic addition to an alkene, or substitution of an alcohol.
The solvent decides whether a halogenoalkane substitutes or eliminates
Primary, secondary and tertiary halogenoalkanes
Nucleophilic substitution
A nucleophile swaps in for the leaving group on a halogenoalkane.
A tertiary halogenoalkane has the halogen on a carbon joined to:
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Primary = 1 carbon attached, secondary = 2, tertiary = 3, on the carbon bearing the halogen.
Match each halogenoalkane idea.
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Each item links the term to its correct meaning.
In nucleophilic substitution, OH⁻ attacks the δ+ carbon and the halogen leaves as a halide ion.
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The C–X bond is polar, so the carbon is δ+ — exactly where an electron-pair donor attacks.
Nucleophilic substitution 亲核取代
- The C–X carbon is slightly positive, so a nucleophile (lone-pair species) attacks and replaces the halogen.
| Reagent | Product |
|---|---|
| $\text{NaOH(aq)}$, heat | an alcohol |
| $\text{KCN}$ in ethanol, heat | a nitrile 腈 (adds a carbon) |
| $\text{NH}_3$ in ethanol, heat + pressure | an amine 胺 |
Many halogenoalkane reactions are carried out by heating under reflux 回流.
Warming a halogenoalkane with aqueous NaOH produces:
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NaOH(aq) substitutes the halogen for –OH, giving an alcohol.
Reaction with KCN in ethanol gives a nitrile, which is useful because it:
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The CN group adds a carbon, lengthening the chain; NH₃ instead gives an amine.
Identifying the halogen
- Warm with silver nitrate in ethanol: a silver halide precipitate forms — white AgCl, cream AgBr, yellow AgI.
Volatile halogenoalkanes were once widely used as refrigerants and aerosol propellants.
You've got it
- a halogenoalkane has a polar C–X bond; classes are primary/secondary/tertiary
- nucleophilic substitution: NaOH(aq) → alcohol; KCN → nitrile (+1 carbon); NH₃ → amine
- identify the halogen with silver nitrate (white/cream/yellow precipitate)