Alkanes Flashcards

1
Q

Alkanes

A

Main component of natural gas, crude oil
Most stable organic compound
Cn H2n+2

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2
Q

Uses

A

Domestic fuel, CH4
Petrol, C5H12
Kerosene, C10H22
Diesel, C12H26

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3
Q

Alkanes bonding

A
Saturated hydrocarbon
Single covalent bond joined to 4 atoms,
Sigma bond results in the overlap of 2 orbitals
Each overlapping orbital has1 electron
4 sigma bonds per C
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4
Q

Alkanes shape

A

4 electron pairs, 4 sigma bonds, axis where atoms rotate freely into different shapes
Tetrahedral, 109.5

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5
Q

Boiling points of alkanes

A

Fractional distillation separates alkanes possible due to its boiling points
Chain length increases, boiling point increases
Chain length increases, surface area increases, more surface contact possible between molecules, more force needed to overcome London Forces

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6
Q

Branching on boiling point

A

Branched isomers have lower boiling point
Fewer surface points of contact between molecules, fewer London forces
Branches get in the way, prevent branched molecules getting close as straight chain molecules, decrease intermolecular forces

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7
Q

Reactivity of alkanes

A

Not reactive with most reagents
Strong sigma bonds
C-C, non polar bonds
Electronegativity of C, H are similar, not polar

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8
Q

Combustion of alkanes, complete

A

Alkanes + Oxygen => Carbon dioxide +Water

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9
Q

Incomplete combustion

A

Hydrogen in alkane oxidised to H2O

Result in CO and water/ Carbon and water

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10
Q

Effects of carbon monoxide

A

Combines irreversibly with haemoglobin to form carboxyhaemoglobin

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11
Q

Reactions of alkanes with halogens

A

UV radiation provides initial energy for reaction

Forms haloalkanes

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12
Q

Radical substitution

A

Bromination of alkanes, show movement of electrons during reaction

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13
Q

Initiation reaction

A

Covalent bond broken by homolytic fission

Very reactive radicals

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14
Q

Propagation reaction

A

Chain reactions

Start and end with a radical

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15
Q

Termination reactions

A

2 radicals collide, forms molecules, ends reactions

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16
Q

Limitations of radical substitution in organic synthesis

A

Further substitution

Substitution at different positions in carbon chain

17
Q

Further substitution

A

Bromomethane collides with bromine radical, forms mixture of haloalkanes

18
Q

Substitution at different positions of carbon chain

A

Methane, 4 hydrogen atoms are bonded to the same carbon, only 1 monobromo compound formed
If chain is longer, mixture isomers formed