15.1 The chemistry of the haloalkanes Flashcards

1
Q

What are haloalkanes

A

Compounds containing the elements carbon, hydrogen and at least one halogen

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2
Q

When naming haloalkanes…

A

…a prefix is added to the name of the longest chain to indicate the identity
Eg. Fluoro- Chloro- Bromo- Iodo-

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3
Q

Haloalkanes have a carbon-halogen bond in their structure. Halogen atoms are more _______ than carbon atoms. The electron pair in the carbon-halogen bond is therefore _______ to the halogen atom than the carbon atom. The carbon-halogen bond is ______.

A

Electronegative
Closer
Polar

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4
Q

Carbon atoms in haloalkanes

A

Have a slightly positive charge and can attract species containing a lone pair of electrons

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5
Q

What are nucleophiles

A

Species that donate a lone pair of electrons

An atom or group of atoms that is attracted to an electron deficient carbon atom

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6
Q

Examples of nucleophiles

A

Hydroxide ions, :OH-
Water molecules, H2O:
Ammonia molecules, :NH3

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7
Q

What happens when a haloalkane reacts with a nucleophile

A

The nucleophile replaces the halogen in a substitution reaction
New compound is produced containing different functional group
Reaction mechanism is nucleophilic substitution

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8
Q

What is substitution

A

A reaction in which one atom or group of atoms is replaced by another atom or group of atoms

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9
Q

What is hydrolysis

A

A chemical reaction involving water or an aqueous solution of a hydroxide that causes the breaking of a bond in a molecule

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10
Q

Steps in nucleophilic substitution

Hydrolysis of haloalkane

A
  1. Nucleophile, OH- approaches carbon attached to halogen on opposite side of molecule
  2. Direction of attack by OH- minimises repulsion between nucleophile and δ- halogen
  3. Lone pair of electrons on OH- ion attracted and donated to δ+ carbon atom
  4. New bond formed between oxygen atom of OH - ion and carbon atom
  5. Carbon-halogen bond breaks by heterolytic fission
  6. New organic product is alcohol, halide ion formed
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11
Q

How can haloalkanes be converted to alcohols

A

By using aqueous sodium hydroxide

Very slow reaction at room temp. so mixture heated under reflux

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12
Q

What do curly arrows show

A

The movement of electron pairs

Start from either lone pair or bonding pair of electrons and point to atom to which it moves

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13
Q

What happens to the carbon-halogen bond in hydrolysis

A

It is broken and the -OH group replaces the halogen in the haloalkane

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14
Q

What does the rate of hydrolysis depend on

A

The strength of the carbon-halogen bond in the haloalkane

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15
Q

Which bond is the strongest
Which is the weakest
C-F, C-Cl, C-Br, C-I

A

C-F is the strongest
C-I is the weakest
Less energy is needed to break C-I bond

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16
Q

Which reacts faster, iodoalkanes or bromoalkanes

A

Iodoalkanes

17
Q

Which reacts faster, bromoalkanes or chloroalkanes

A

Bromoalkanes

18
Q

Fluoroalkanes are unreactive because…

A

…a large quantity of energy is required to break the C-F bond

19
Q

How can we measure the rate of hydrolysis of primary haloalkanes

A

Carry out rewaction in presence of aqueous silver nitrate
Halide ions produced which react with Ag ions to form precipitate of silver halide
Nucleophile in reaction is water
Haloalkanes are insoluble in water and reaction carried out in presence of ethanol solvent

20
Q

Why do we use ethanol when measuring the rate of hydrolysis of primary haloalkanes

A

It allows water and the haloalkane to mix and produce a single solution rather than two layers

21
Q

Required practical detailed method

Hydrolysis of haloalkanes

A
  1. Set up 3 test tubes of haloalkanes with 1cm^3 ethanol
  2. Stand tubes in water bath at 60 degrees
  3. Place test tube containing 0.1moldm^-3 silver nitrate in water bath, allow all to reach constant temp.
  4. Add 1cm^3 silver nitrate quickly to each test tube
  5. Start stop clock
  6. Observe for 5 mins and record time taken for precipitate to form
22
Q

Hydrolysis of haloalkanes - The compound with the slowest rate of reaction is the one that has the ______ carbon-halogen bond

A

Strongest

23
Q

The rate of hydrolysis increases as the strength of the carbon-halogen bond…

A

…Decreases.

24
Q

Which is hydrolysed the fastest, a primary haloalkane, secondary or tertiary

A

Primary is slowest, tertiary is fastest

Primary reacts by one-step mechanism while tertiary is two-step

25
Q

Two step mechanism of a tertiary haloalkane

A
  1. Carbon-halogen bond breaks by heterolytic fission forming tertiary carbocation and halide ion
  2. Hydroxide ion attacks carbocation to form organic product