Preparation of alkanes1 concept
(odd C)
| Method | C in | C out | Product |
|---|---|---|---|
| Wurtz: 2 C₂H₅Br + 2 Na | 2 | 4 | |
| Kolbe: 2 CH₃COONa | 2 | 2 | |
| soda lime: C₂H₅COONa | 3 | 2 | |
| Zn/HCl: C₂H₅Br | 2 | 2 |
- Soda lime: one C fewer. Reduction keeps the C count; Zn/dil. HCl reduces RCl, RBr, RI but not RF.
- Quick method. Halides that give one alkane by reduction (Zn/HCl, or RMgX then water) = its monohalo structural isomers: 2-methylbutane has four distinct C–H sets, so 4 RBr.
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6 more concepts in 2 topics
Free-radical halogenation and Conformations and properties. Read the first part free. Sign in free with Google to read the rest and download the PDF.
Free-radical halogenation3 concepts
- Mechanism: initiation to termination2×
- Selectivity: 3° > 2° > 1° H3×
- Counting halogenation products4×
Conformations and properties3 concepts
- Staggered vs eclipsed ethane
- Boiling and melting points1×
- Combustion and controlled oxidation2×
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