alkanes: content Flashcards

1
Q

general formula for alkanes

A

CₙH₂ₙ₊₂

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2
Q

general formula for cycloalkanes

A

CₙH₂ₙ (same as alkenes)

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3
Q

how are alkanes bonded

A

sigma (σ) bonds (strongest type of covalent bond)

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4
Q

complete combustion equation

A

alkane + oxygen → carbon dioxide + water

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5
Q

equations for incomplete combustion

A

alkane + oxygen → carbon monoxide + water
alkane + oxygen → carbon + water

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6
Q

issues with incomplete combustion

A
  • 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
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7
Q

free radical substitution: overall equation

A

halogen + alkane →UV light→ haloalkane + hydrogen halide
(substitution reaction)

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8
Q

free radical substitution mechanism

A

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

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9
Q

issues with free radical substitution

A

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

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