Free radical substitution Flashcards

a review of the terms and steps in free radical substitution mechanism

1
Q

Is bond breaking endothermic or exothermic?

A

endothermic

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2
Q

Is bond forming endothermic or exothermic?

A

exothermic

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3
Q

What does exothermic mean?

A

The formation of products give out energy to the surroundings

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4
Q

What does endothermic mean?

A

The formation of products takes in energy from the surroundings

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5
Q

What do we call a bond breaking and the electrons being returned to their original atoms?

A

Homolytic fission

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6
Q

What do we call as substance with an unpaired electron?

A

free radical

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7
Q

What energy source is used to cause a halogen bond to undergo homolytic fission?

A

Ultra Violet (UV) radiation

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8
Q

What do we call Group VII elements?

A

Halogens

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9
Q

How many hydrogen halides are made for every halogen substitution into the alkane? ​

A

Each substituted halogen creates a hydrogen halide.

e.g. C3H10 + 3Cl2 → C3H7Cl3 + 3HCl

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10
Q

What are the 3 steps in a free radical mechanism called?

A
  1. initiation
  2. propagation
  3. termination
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11
Q

Give an equation for an initiation step in the mechanism using chlorine

A

UV light breaks Cl2 down to form chlorine free radicals.​

Cl2 → 2Cl●​

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12
Q

What happens in the first part of the propagation step? Give an equation for methane reacting with Cl● .

A

The alkane reacts with the halogen radical.​

An H atom is removed from the alkane to produce a hydrogen halide and a hydrocarbon free radical.

Cl● + CH4 → HCl + ●CH3

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13
Q

What happens in the second part of the propagation step? Give an equation for methane reacting with Cl● .

A

The hydrocarbon free radical reacts with the halogen to put a halogen atom onto the hydrocarbon free radical.​

e.g. ●CH3 + Cl2 → Cl● + CH3Cl​

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14
Q

Why is the propagation step a chain reaction?

A

It makes more free radicals which can react again and again.

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15
Q

What is a termination step?

A

Termination is any step that does not produce free radicals.

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16
Q

if methane and chlorine react in the presence of UV; what would be a termination step that gave a halogenoalkane?

A

Cl● + ●CH3 → CH3Cl

17
Q

if methane and chlorine react in the presence of UV; what would be a termination step that gave a alkane?

A

●CH3 + ●CH3 → C2H6​

18
Q

Why don’t chemists use free radical mechanism to make halogenoalkanes?

A

It produces a mixture of many products.