Alkanes Flashcards

1
Q

what are alkanes

A
  • saturated hydrocarbons (each carbon is bonded 4x with maximum no. of H)
  • CnH2n+2
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2
Q

what is the shape of an alkane

A
  • tetrahedral around the carbon atom
  • bond angle of 109.5
  • the bonds repel each other equally
  • electrons AFAP
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3
Q

size of molecule related to forces

A
  • the bigger the molecule the more induced dipole-dipole forces as you have larger electron clouds
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4
Q

when boiling, what is being broken

A
  • when you boil a liquid the weak induced dipole dipole forces are broken
  • NOT the covalent bonds
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5
Q

effect of chain length on BP

A
  • chain length increases
  • BP increases
  • molecules have larger SA
  • more surface contact
  • greater London forces
  • more energy needed to overcome forces
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6
Q

effect of branching on BP

A
  • lower BP
  • fewer surface points of contact
  • fewer London forces
  • molecules cant get as close because branches are in the way
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7
Q

Describe the complete combustion of alkanes

A
  • alkanes burn in oxygen completely to form co2 and water
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8
Q

why are alkanes good fuels?

A
  • burn readily to produce large amounts of energy
  • readily available
  • easy to transport
  • burn in plentiful o2 without producing any toxic products.
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9
Q

describe the incomplete combustion of alkanes

A
  • limited oxygen = H-atoms in alkane are oxidised to water

- CO or C(soot) formed due to incomplete combustion of C

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10
Q

describe CO and soot

A
  • poisonous, colourless and odourless gas
  • binds to haemoglobin and prevents oxygen bonding
    CO can be removed using a catalytic converter
  • soot can cause breathing problems
  • dirty building
  • clog up engines
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11
Q

Describe the reaction of alkanes with halogens

A

initiation:
- the covalent bond in the Halogen(Br2) is broken by homolytic fission
- energy for this bond fission is provided by UV
- each bromine takes an electrons from the shared pair forming 2 Br radicals:
Br-Br = Br• + Br•

propagation:
- the reaction propagates through 2 propagation steps - a chain reaction :
CH ₄ + Br• = •CH₃ + HBr
•CH₃ + Br₂ = CH₃Br + Br•

Termination:
- when 2 radicals collide, forming a molecule with all electrons paired
Br• + Br• = Br₂
•CH₃ + •Br = CH₃Br

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12
Q

why do alkanes lack reactivity

A
  • C-C and C-H bonds are strong
  • C-C bonds are non-polar
  • EN of C+H is so similar that the C-H bond can be considered non-polar.
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13
Q

limitations of radical substitution

A
  • further substitution occurs producing a variety of products (which have to be separated due to being impurities)
  • substitution can occur at different points on the carbon chain (isomers)
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14
Q

how to reduce the further substitution in radical

A
  • adding excess organic compound (methane)

- there is a greater chance of the halogen (chlorine) reacting with the methane.

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