alkanes: content Flashcards
general formula for alkanes
CₙH₂ₙ₊₂
general formula for cycloalkanes
CₙH₂ₙ (same as alkenes)
how are alkanes bonded
sigma (σ) bonds (strongest type of covalent bond)
complete combustion equation
alkane + oxygen → carbon dioxide + water
equations for incomplete combustion
alkane + oxygen → carbon monoxide + water
alkane + oxygen → carbon + water
issues with incomplete combustion
- less exothermic than complete combustion
- less cost-effective
- carbon monoxide forms dative covalent bonds to haemoglobin
- irreversible and strong
- reduces blood oxygen concentration and blocks cell respiration
free radical substitution: overall equation
halogen + alkane →UV light→ haloalkane + hydrogen halide
(substitution reaction)
free radical substitution mechanism
initiation (creating free radicals)
X₂ →UV light→ 2X⋅
propagation (molecule + radical → molecule + radical)
1ˢᵗ: CₙH₂ₙ₊₂ + X⋅ → ⋅CₙH₂ₙ₊₁ +HX
2ⁿᵈ: ⋅CₙH₂ₙ₊₁ + X₂ → CₙH₂ₙ₊₁ +X⋅
this step is self-propagating and will continue until you run out of reactants
termination (two radicals combine to form a molecule)
two halogen radicals combine
a halogen radical combines with an alkyl radical
two alkyl radicals combine
issues with free radical substitution
yields tend to be low
- further substitution can occur, forming a mixture of difficult-to-isolate products
- substitution can occur in different positions, creating position isomers