Alkanes Flashcards

1
Q

what are alkanes

A

saturated hydrocarbons containing single, sigma C-C and C-H bonds

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2
Q

why are alkanes not very reactive

A
  • high bond enthalpy
  • low polarity of the sigma bonds
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3
Q

what are sigma,σ, bonds

A

direct overlap of s orbitals

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4
Q

angle around C atom in alkanes and explanation

A
  • 109.5 degrees
  • 4 bonding pairs of e- around C repel equally to give a tetrahedral shape
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5
Q

how does chain length affect boiling point

A
  • longer chain length increases London forces between molecules as theres more surface contact and more electrons to interact
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6
Q

why does branching decrease boiling point of alkanes

A
  • branched alkanes can’t pack as clodely together as straight chains
  • More branching gives less (surface) contact
  • fewer/weaker London forces
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7
Q

why are alkanes used as fuels

A
  • readily undergo combustion
  • release a lot of energy due to very exothermic combustion enthalpy changes
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8
Q

when does complete combustion occur

A
  • when there is sufficient oxygen
  • burns with a clean, often blue flame
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9
Q

products of complete combustion

A
  • CO2 and H2O
  • both greenhouse gases known to contribute towards global warming
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10
Q

when does incomplete combustion occur

A

when there is limited supply of oxygen and burns with a dirty yellow flame

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11
Q

products of incomplete combustion

A
  • CO and H2O
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12
Q

dangers of CO

A
  • colourless, odourless, highly toxic gas
  • combines with Hb, blocking transport of O2 to cells
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13
Q

what do alkanes need to undergo free radical substitution

A
  • halogen
  • UV light
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14
Q

what does free radical substitution form

A

haloalkanes

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15
Q

what are the three steps in free radical substitution

A
  1. initiation
  2. propagation
  3. termination ( multiple reactions can occur)
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16
Q

free radical substitution of hexane with bromine

A

1) Br2 —> 2Br*
2) Br * + C6H14 —> C6H13* + HBr​
C6H13* + Br2 —> C6H13Br + Br*
3) Br* + Br* —> Br2​
C6H13* + C6H13* —> C12H26
C6H13* + Br* —> C6H13Br