11 Alkenes Flashcards
CH₃CH₂X → CH₂CH₂ + HX
Elimination:
Ethanolic KOH, heat
CH₃CH₂OH → CH₂CH₂ + H₂O
Elimination:
Excess conc. H₂SO₄ / Al₂O₃ / H₃PO₄, heat
CH₂CH₂ → CH₃CH₃
Reduction:
H₂, [ Ni, heat / Pt, Pd ]
CH₂CH₂ → CH₃CH₂X
Electrophilic addition:
Dry HX(g)
CH₂CH₂ → CH₂XCH₂X
Electrophilic addition:
X₂ in CCl₄
CH₂CH₂ → CH₂XCH₂OH
Electrophilic addition:
X₂(aq)
CH₂CH₂ → CH₃CH₂OH
Electrophilic addition:
Cold conc. H₂SO₄, then H₂O /
H₂O with H₃PO₄ catalyst
CH₃CHCH₂ → CH₃COOH + CO₂ + H₂O
Strong oxidation (Acidic):
KMnO₄(aq), H₂SO₄(aq), heat
CH₃CHCH₂ → CH₃COO⁻Na⁺ + Na₂CO₃ + H₂O
Strong oxidation (Basic):
KMnO₄(aq), NaOH(aq), heat
CH₂CH₂ → CH₂(OH)CH₂OH
Mild oxidation:
KMnO₄(aq), H₂SO₄ / NaOH (aq), cold
Reactivity of Alkenes
Generally reactive:
Electron-rich C=C bond attracts electrophiles
Reactivity of Alkenes
Generally reactive:
Electron-rich C=C bond attracts electrophiles