Organic Chemistry: Alkanes, Alkenes, Alcohols and Haloalkanes Flashcards

1
Q

What are alkanes?

A

A saturated hydrocarbon where each carbon is surrounded by four pairs of electrons.

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2
Q

What is the general formula of alkanes?

A

CₙH₂ₙ₊₂

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3
Q

How and why does boiling point vary as the chain length of alkanes increase?

A

The boiling point increases with chain length because a longer chain length means that there’s more points of contact for London Forces. Consequently, less energy is required to break the London Forces.

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4
Q

How does branches in Alkanes affect boiling point?

A

Branched isomers have lower boiling points because the branches result in fewer points of contact resulting in less London Forces. Consequently, less energy is required to break the London Forces.

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5
Q

How do you obtain specific chemicals from crude oil?

A

Distillation.

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6
Q

Why are Alkanes not very reactive?

A

Because σ bonds are quite strong. C-C bonds are non-polar and C-H bonds are so similar in electronegativity that they might as well be non-polar.

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7
Q

What makes Alkanes good combustors?

A

They are easy to obtain, Easy to transport, do not release toxins when combusted and burn in plentiful oxygen supply.

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8
Q

What are Alkenes?

A

Unsaturated hydrocarbons with at least one carbon-carbon in the structure.

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9
Q

What is the general formula of alkenes?

A

CₙH₂ₙ

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10
Q

What two bonds make up a carbon-carbon double bond.

A

π bond and σ bond

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11
Q

What do π bonds do to the structure of alkenes?

A

The π bond locks the rotation of the molecule at the double bond.

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12
Q

How are π bonds formed?

A

π bonds are the sideways overlap of p-orbitals and are located above and below the σ bond. One electron is taken from each carbon to make the bond.

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13
Q

What is the shape and bond angle of atoms around the double bond?

A

The angle is 120° and the shape is trigonal planar.

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14
Q

What is a σ bond?

A

The overlap and sharing of two electrons. (Basically a covalent bond)

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15
Q

In alkanes, what is the shape and bond angle of a carbon atom surrounded by 4 other atoms.

A

The angle is 109.5° and the shape is a tetrahedral one.

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16
Q

Why does stereo isomerism only occur in Alkenes?

A

Because the rigid double bond locks the rotation of the alkene.

17
Q

When does stereo isomerism occur?

A

When there’s a double bond and two different groups on both sides of the double bond.

18
Q

Why are alkenes more reactive than alkanes?

A

Because the π bonds electrons are on the outside of the double bond and are therefore easier to pull away making them not as strong as the σ bond.

19
Q

What are polymers?

A

Extremely large molecules made up of small monomers which are in repeating units.

20
Q

What are downsides with man-made polymers?

A

Most polymers don’t biodegrade meaning they don’t break down naturally.
Large dumping of polymers can endanger wildlife and marine life.
Some polymers like PVC can release toxins (e.g. hydrogen chloride) into the air when burnt

21
Q

What is an alcohol?

A

A molecule with the -OH functional group.

22
Q

Why are alcohols less volatile and have higher melting points when compared to alkanes?

A

Because in alcohols, the intermolecular forces holding the molecules together are actually hydrogen bonds. Hydrogen bonds are a lot stronger and require more energy to break compared to London forces which are weaker. Therefore, alcohols need more energy to change state and have a higher boiling point.

23
Q

How does the differences between alcohols and alkanes change with chain length?

A

The difference between alkanes and alkenes gets smaller as chain length increases.

24
Q

Why do alcohols have higher water solubility than alkanes?

A

Alcohols have hydrogen bonds allowing them to form bonds with water. Alkanes have no hydrogen bonds so they can’t form bonds with water.

25
Q

How does increasing chain length in alcohols affect the water solubility?

A

As chain length increases, alcohols become less soluble as the -OH functional group has less influence.

26
Q

What is a haloalkane?

A

A compound containing the elements carbon and hydrogen with at least one halogen.

27
Q

Out of these bonds which is the strongest and which is the weakest? C-F C-Cl C-Br C-I

A

C-F Is the strongest

C-I is the weakest

28
Q

What is the Ozone layer?

A

A layer in our atmosphere that absorbs dangerous UV radiation from the sun.

29
Q

What is Ozone?

A

O₃

30
Q

What are CFC’s?

A

Chlorofluorocarbons.

31
Q

What are the problem with CFC’s?

A

CFC’s break down when exposed to UV light producing chlorine radicals. These chlorine radicals speed up the depletion of the Ozone layer.

32
Q

How do we test the reactivity of haloalkanes?

A

Place the chloroalkane, bromoalkane and iodoalkane into three separate tubes and add silver nitrate with ethanol to each tube. Then time how long it takes for the precipitate to form in each one.

33
Q

How do CFC’s speed up the depletion of the Ozone layer?

A

1) UV light breaks down C-Cl bond into 2 Cl•
2) Cl• + O₃ —> ClO• + O₂
3) ClO• + O₃ —> 2O₂ + Cl•
4) Overall Equation: 2O₃ —> 3O₂

34
Q

Apart from Chlorine radicals, what other radicals can destroy Ozone?

A

Nitrogen Oxides from vehicle emissions and thunderstorms can destroy Ozone

35
Q

Why did we use CFC’s in the first place?

A

They were stable, unreactive and non-toxic meaning they were ideal for refrigerators and propellants.