module 4.1.2 - alkanes Flashcards

1
Q

what is the general formula of alkanes?

A

C(n)H(2n+1)

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2
Q

why are alkanes non-polar?

A

there’s no significant difference between the electronegativities of carbon and hydrogen

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3
Q

give 1 use of alkanes

A

fuels

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4
Q

explain the shape and bond angles in an alkane

A

there are 4 bonding pairs and 0 lone pairs around each carbon. all electron pairs repel. lone pairs repel more than bonding pairs. bong angle is 109.5.

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5
Q

explain how sigma bonds are formed in alkanes

A

the end on end overlap of bonding orbitals directly between atoms. how well they overlap determines the strength of the bond.

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6
Q

bonds can __________ in an alkane

A

rotate

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7
Q

explain the relative melting and boiling points of 2 alkanes with different chain lengths.

A

as chain length increases, boiling/melting point increases, as they have a greater surface area so have more points of contact between molecules. this means strength of induced dipole-dipole interactions increases, which require more energy to overcome.

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8
Q

explain the relative melting and boiling points of branched isomers

A

the more branches there are in an isomer molecule, the lower the boiling point. the branches cause fewer points of surface contact between molecules so induced dipole-dipole interactions are weaker and require less energy to overcome.

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9
Q

explain why production of carbon monoxide in the combustion of alkanes is bad.

A

carbon monoxide is poisonous. leads to oxygen deprivation, which causes fatigues, headaches and nausea.

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10
Q

are straight chain or branched chain isomers more efficient in combustion reactions?

A

branched

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11
Q

what is a radical?

A

highly reactive species with an unpaired electron.

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12
Q

what is homolytic fission?

A

covalent bond breaks and one electron goes to each atom forming 2 radicals.

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13
Q

what is heterolytic fission?

A

covalent bond breaks and both electrons go to the same atom forming 2 ions

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14
Q

what does a curly arrow represent?

A

movement of an electron pair

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15
Q

what are the 3 steps for free radical substitution and what conditions are required

A

1- initiation (radicals are made)
2 - propagation (radicals are used up and created)
3 - termination (radicals combine to make a neutral molecule)
conditions - UV and high temperature

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16
Q

what are the drawbacks of free radical substitution?

A

multi-substitution occurs (can overcome this by using excess alkane). substitution can occur anywhere along the chain, so a mixture of isomers forms

17
Q

explain the importance of ozone

A

absorbs UV radiation. reduced the amount of UV at the earths surface. UV radiation causes sunburn and skin cancer.

18
Q

explain the natural formation of ozone

A

ozone absorbs UV radiation
UV at Earth’s surface is reduced
(UV) O2 –> 2O.
O2 + O. –> O3

19
Q

what is a chlorofluorocarbon?

A

contain chlorine, fluorine and carbon only - all hydrogens have been substituted.

20
Q

give 3 properties of chlorofluorocarbons

A

volatile, non-flammable and non-toxic

21
Q

give 4 (past) uses of chlorofluorocarbons

A

aerosol cans, dry cleaning, air conditioning and fridges

22
Q

why are chlorofluorocarbons no longer used?

A

they were destroying the ozone layer. they catalyse the breakdown of ozone

23
Q

what is the overall equation for the breakdown of ozone?

A

O3 + O –> 202 (with Cl. or NO. catalyst)

24
Q

NO. radical destroy the ozone layer. how are nitrogen oxides formed?

A

produces by lighting in thunderstorms and in car/aircraft engine

25
Q

what are hydrochlorofluorocarbons/hydrofluorocarbons and why are they more widely used than chlorofluorocarbons?

A

HCFCs and HFCs are used as an alternative to CFCs until safer products are developed. HCFCs are broken down in the atmosphere much more quickly (10-20 years whereas CFCs take 90 years). HFCs done contain Cl so done affect the oxone layer. HCFCs and HFCs are greenhouse gases

26
Q

give 3 alternatives to CFCs (not inc HCFCs or HFCs)

A

aerosols with pump sprays/nitrogen propellants
fridges/freezers using ammonia as the coolant gas
CO2 is used to make expanded polymers.