4.1.2 - Alkanes Flashcards

1
Q

What is the general formula for alkanes?

A

CnH2n+2

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2
Q

What are alkanes?

A

Saturated hydrocarbons containing single C-C and C-H bonds as sigma bonds.

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3
Q

What are sigma bonds?

A

Overlap of orbitals directly between the bonding atoms.

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4
Q

What is there around the sigma bond?

A

Free rotation.

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5
Q

What is the shape of alkanes around each carbon?

A

Tetrahedral

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6
Q

What happens and why to the boiling point of straight chain alkanes as you increase chain length?

A

Boiling point increases as the number of electrons in molecule increases and there is more surface contact resulting in an increase in strength of london forces.

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7
Q

Why do branched alkanes have lower boiling points?

A

They can’t pack as closely together and they have smaller molecular surface areas so induced dipole-dipole interactions are reduced.

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8
Q

What is produced in the complete combustion of alkanes?

A

Carbon dioxide and water.

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9
Q

What is produced in the incomplete combustion of alkanes?

A

Carbon monoxide and water.

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10
Q

What is a tip that’s good to know when balancing combustion reactions?

A

Balance carbons first, then hydrogens and then oxygens.

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11
Q

Why is carbon monoxide poisonous?

A

It is better at binding to the haemoglobin than oxygen, which means less oxygen will be carried around your body leading to oxygen deprivation.

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12
Q

Name the type of mechanism which leads to the formation of bromo/chloromethane?

A

Free radical substitution.

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13
Q

What is reaction and what happens in initiation?

A

Cl2 -> (UV) 2Cl. - This is homolytic fission.

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14
Q

What happens in propagation 1?

A

CH4 + Cl. -> HCl + CH3.

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15
Q

What happens in propagation 2?

A

CH3. + Cl2 -> CH3Cl + Cl.

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16
Q

What are the terminal reactions?

A

CH3. + Cl. -> CH3Cl
Cl. + Cl. -> Cl2
CH3. + CH3. -> C2H6

17
Q

Why is ethane produced as trace?

A

As two methyl radicals have bonded together to form it.

18
Q

What happens when two radicals join together?

A

They make stable molecules.

19
Q

What is the major product formed when a large excess of chlorine reacts with methane in the presence of UV light?

A

CCl4 - tetrachloromethane

20
Q

What are the limitations of radical substitution in synthesis?

A

A mixture of products is produced, therefore you have to separate the desired product from the others. Moreover it can take place at any point along the carbon chain, so a mixture of isomers can be formed.