halogenoalkanes Flashcards

1
Q

describe a nucleophile

A

nucleophile – they
always have a lone pair and act as
electron pair donator

The nucleophiles
attack the positive
carbon atom

We use curly arrows in mechanisms (with
two line heads) to show the movement of
two electrons

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2
Q

describe nucleophyllic reaction of aqueous hydroxide ions

A

the reaction causes the Change in functional group: halogenoalkane to alcohol

Reagent: potassium (or sodium) hydroxide

Conditions: In aqueous solution; Heat under reflux

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3
Q

the effect of CFCs

A

Man-made chlorofluorocarbons (CFC’s) caused a hole to form in the ozone
layer.

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4
Q

the effects of chlorine radical on ozonen

A

The chlorine free radical atoms catalyse the decomposition of ozone, due to these reactions,
because they are regenerated.

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5
Q

the free radical substitution for ozone

A

Cl . + O3 —> ClO. +02

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6
Q

what are the uses of halogenoalkanes

A

used as solvents.
Uses of Halogenoalkanes
Halogenoalkanes have also been
used as refrigerants, pesticides
and aerosol propellant

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7
Q

what is ozone

A

Ozone in the lower atmosphere
is a pollutant and contributes
towards the formation of smog.

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8
Q

how are chlorine radicals formed

A

Chlorine radicals are formed in the upper atmosphere when energy from ultra-violet radiation causes C–Cl bonds in chlorofluorocarbons (CFCs) to
break.

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9
Q

where are HFCS and why are they safer

A

HFCs (Hydro fluoro carbons) e.g. CH2FCF3 are now used for refrigerators
and air-conditioners. These are safer
as they do not contain the C-Cl bond

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10
Q

what effects the rate of substitution reactions

A

The rate of these substitution reactions depends on the strength
of the C-X bond
The weaker the bond, the easier it is to break and the faster the reaction

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11
Q

what is used to test the reactivity of halogenoalkanes

A

silver nitrate

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12
Q

what causes the precipitate to form in a halogenoalkane reaction

A

The precipitate only forms when the halide ion has left the
halogenoalkane and so the rate of formation of the precipitate
can be used to compare the reactivity of the different
halogenoalkanes.

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