4.1.2 Alkanes Flashcards

1
Q

What happens during orbital hybridisation?

A

When the orbitals mix together to form new hybrid orbitals.

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2
Q

Explain the correlation between boiling point and chain length in alkanes.

A

As the chain length increases so does the surface area of contact between molecules, this means there is more London dispersion forces so more energy is needed to overcome the forces.

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3
Q

How does branching affect bp?

A

Less surface area of contact between molecules.

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4
Q

What are alkanes?

A

The alkanes are saturated hydrocarbons containing single C-C and C-H bonds as sigma bonds

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5
Q

What are cycloalkanes?

A

The cycloalkanes are a homologous series of hydrocarbons with the general formula CnH2n and names beginning cyclo– and ending in –ane.

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6
Q

What is bond enthalpy?

A

the amount of energy required to break one mole of a specific covalent bond in a gaseous molecule

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7
Q

Why are alkanes general unreactive? Give 2 reasons.

A

1) C-C and C-H bonds have high bond enthalpy which means there relatively difficult to break.

2) C-C bonds are non polar so C-H bonds have high polarity.

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8
Q

In what order do you balance in combustion?

A

Carbon
Hydrogen
oxygen

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9
Q

What would happen if there was even less oxygen then needed incomplete combustion?

A

Carbon particulates are formed.

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10
Q

Why is carbon monoxide dangerous for the body?

A

It binds with the haemoglobin and is carried instead of oxygen.

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11
Q

what is a fuel?

A

a substance when burned releases heat energy

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12
Q

3 types of cracking

A

thermal
steam
catalyst

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13
Q

Why do cycloalkanes have higher bp then its straight chain alkane?

A

There is a strain in the molecule which means more energy to break London dispersion forces.

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14
Q

What type of isomer is a cycloalkene

A

structural isomer

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15
Q

Features/quality of alkanes:

A

non polar
insoluble in water
less dense then water
hydrophobic it repels in water
cannot conduct - all e- used
no e- can move
low mp
simple covalent

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16
Q

What are the 3 main types of attackers and what do they do?

A

nucleophile - donates a lone pair of electron to an electron deficient area (to form a new bond)

Electrophile - electron pair acceptor

radical - unpaired electrons usual reactive

17
Q

What is it called when chemical reaction bonds are broken?

A

bond fission

18
Q

2 types of bond fission?

A

Hetrolytic and homolytic

19
Q

Conditions for free radical substitution?

A

Uv light
Excess methane to reduce further substitution?

20
Q

What is a mechanism

A

Multiple steps to a reaction

21
Q

What happens in the initiation step?

A

The starting of the reaction that produces 2 radicals using uv - homiletic fission

22
Q

What happens in propagation?

A

A 2 step process that combine to form an overall equation where the same species cancel out. Has to be 2 radicals on each side of the equation

23
Q

Termination step?

A

The 2 radicals react together

24
Q

Why is the initiation step an example of homolytic fission?

A

Because one election from bond pair goes to each atom/ forms two radicals

25
Q

Difference in terms of intermolecular forces of alkanes compared to alcohols.

A

Alcohol have hydrogen bonding and London dispersion forces but the hydrogen bonding is stronger then the alkanes ldf.

26
Q

what is meant by homologous series?

A

A series of compound elements with the same functional group with successive members differering by ch2

27
Q

explain why the mechanism for free radical substitution is likely to produce a mixture of organic products?

A

it can substitute any of h atoms