Halogenoalkanes Flashcards

1
Q

How do halogenoalkanes form?

A

Through the placing a mixture of an alkane an a haloen into bright sunlight, the UV components of the ligh starts the reaction.

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2
Q

Why cannot halogenoalkans form in a dark room at room temperature?

A

This is because the reaction relys on the UV present in the light.

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3
Q

What type of reaction is the formation of halogenoalkanes?

A

A free-radical substitution.

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4
Q

What are the stages of a the free radical substitution reaction of the formation of halogenoalkanes?

A

Initiation, propagation and termination.

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5
Q

What is the initiation stage of a free-radical substitution reaction?

A

The breaking of the diatomic molecule to form two atoms which are free radicals. This happens due to the bond absorbing the energy of a single quantam of UV. These free radicals are highly reactive.

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6
Q

Why does the alkane not break down during the initiation step?

A

The energy of available in the UV light is not enough to break the C-H bond.

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7
Q

What are halogenoalkanes?

A

Alkanes with one or more halogens attached to it.

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8
Q

Explain the trend in boiling points of halogenoalkanes.

A

The boiling points increase down the group, this is due to the strength of intermolecular forces. Van der waals forces get stronger witg more electrons.

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9
Q

Why are halogenoalkanes attacked by nucleophiles?

A

They have a polar bond.

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10
Q

In which direction are the electrons pulled towards in a halogenoalkane and why?

A

Towards the halogens as the halogens are more electronegative than the carbons.

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11
Q

What is a nucleophile?

A

A substance that is an electron pair donor.

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12
Q

What are three examples of nucleophiles?

A

Ammonia
Hydroxide Ions
Cyanide Ions

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13
Q

How do halogenoalkanes react with hydroxide ions?

A

Via nucelophilc substitution.

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14
Q

What are the conditions for the nucleophilic substiution involving halogenoalkanes and hydroxide ions?

A

Warm aqueous sodium hydroxide and it is carried under reflux.

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15
Q

What do halogenoalkanes react with cyanide ions to make?

A

Nitriles.

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16
Q

What are the conditions for the reaction between cyanide ions and halogenoalkanes?

A

Warm ethanolic potassium cyanide and it is carried out under reflux.

17
Q

What does the nucleophilic substitution of halogenoalkanes with hydroxide ions create?

A

Alcohols.

18
Q

How do halogenoalkanes react with ammonia?

A

Via nucleophilic substitution.

19
Q

What are the conditions of the nucleophilic substitution of halogenoalkanes with ammonia?

A

Heat with ethanolic ammonia and an excess of ammonia.

20
Q

What is produced from the nucleophilic substitution of halogenoalkanes and ammonia?

A

An amine.

21
Q

Describe the trend in reactivity of halogenoalkanes down the group.

A

Reactivity increases dow the group.

22
Q

How do halogenoalkanes react with hydroxide ions via elimination?

A

Using ethanol solvent.

23
Q

What solvent does the elimination reaction of halogenoalkanes with hydroxide ions require?

A

Ethanol solvent.

24
Q

What are the conditions of the elimination reaction of halogenoalkanes and hydroxide ions?

A

Warm ethanolic sodium hydroxide and it is carried out under reflux.

25
Q

What does the elimination reaction between halogenoalkanes and hydroxide ions produce?

A

An alkene.

26
Q

What do chlorofluorocarbons break down in the atmosphere?

A

Ozone.

27
Q

Why are C-Cl bonds broken the easiest by UV?

A

They have the lowest bond enthalpy.

28
Q

What is an alternative to CFC’s?

A

Hydrofluorocarbons.

29
Q
A