Chapter 14 Flashcards

1
Q

What is the general formula for an alcohol?

A

CnH2n+1OH

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2
Q

What functional group to alcohols contain?

A

A OH functional group.

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3
Q

What are the properties of alcohols?

A

They have high melting and boiling points, so a less volatile and have a greater water solubility than alkanes.

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4
Q

Why have alcohols got a high melting and boiling point?

A

As alcohols are polar molecules due to the O – H polar bond there is a difference in electronegativity between oxygen and hydrogen. The intermolecular forces are weak London forces as well as strong hydrogen bonds between the polar groups. Therefore they require more energy to overcome and break the bonds.

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5
Q

Why are they soluble in water?

A

They are soluble in water due to the influence of the OH group in the hydrocarbon chain as hydrogen bonds form between the OH and the water molecule.

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6
Q

What happens to the solubility as the chain length increases?

A

As the hydrocarbon chain increases the influence of the OH group becomes relatively smaller and the solubility of the longer chain becomes less soluble (solubility decreases).

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7
Q

Are they more or less soluble than alkanes?

A

They are more soluble than alkanes due to alkanes being non polar so can’t form hydrogen bonds with water whereas alcohols can form hydrogen bonds with water meaning they are soluble in water.

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8
Q

Why do they have a low volatility?

A

In the liquid state hydrogen bonds hold the alcohol together, bonds need to be broken to change its state which requires more energy than breaking a weak bonds found in alkanes. Alcohols have a lower volatility than alkanes.

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9
Q

What is viscosity?

A

It is the measure of a fluid resistance to flow

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10
Q

What is a primary alcohol?

A

The OH group is attached to 2 hydrogens or one carbon atom.

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11
Q

What is a secondary alcohol?

A

The OH group is attached to a carbon atom that is attached to one hydrogen or two other carbon atoms.

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12
Q

What is the tertiary alcohol?

A

The OH group is attached to no hydrogens on the carbon atom and three carbon atoms

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13
Q

What happens as the chain length increases in terms of the quantity of heat released.

A

The quantity of heat release per mole increases.

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14
Q

What is the usual oxidising mixture?

A

Potassium dichromate acidified with dilute sulphuric acid.

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15
Q

What happens in terms of a colour change if the alcohol is oxidised?

A

It changes colour from an orange solution to a green solution as it has been reduced. The orange solution contains dichromate ions and the reduced solution contains chromium ions.

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16
Q

What can a primary alcohol oxidise into?

A

An aldehyde or carboxylic acid.

17
Q

What is a secondary alcohol oxidised into?

A

A ketone

18
Q

What is a tertiary alcohol oxidised into?

A

It’s cannot be oxidised as there are no hydrogen bonded to the carbon carrying the hydroxyl group.

19
Q

How is an aldehyde prepared?

A

It forms when the primary alcohol is gently heated with acidified potassium dichromate. It is then distilled out of the reaction mixture whilst forming, preventing any further reaction.

20
Q

How is a carboxylic acid prepared?

A

The primary alcohol is heated strongly under reflux with an excess of potassium dichromate acidified. An excess of the oxidising agent insures that all the alcohol has been oxidised. Heating under reflux insures that the initial aldehyde undergoes oxidisation to form a carboxylic acid.

21
Q

How are ketones prepared?

A

They are prepared by heating under reflux in order to make sure the reaction is complete which are oxidised with acidified dichromate ions.

22
Q

What happened to the solution of tertiary alcohols?

A

It will remain orange when an alcohol is added.

23
Q

What is dehydration of alcohols?

A

It is when a water molecule is removed from the starting material in a reaction. And alcohol was heated under reflux in the presence of an acid catalyst e.g. concentrated sulphuric acid or concentrated phosphoric acid. The product is an alkene.

24
Q

What type of reaction is dehydration of an alcohol?

A

It is an elimination reaction where small molecule is removed from a large molecule forming an unsaturated molecule.

25
Q

What is the substitution reaction of alcohols?

A

It is when alcohol is react with hydrogen halides to form halo alkanes. A haloalkane is formed when the halide and alcohol is heated under reflux with sodium halides and sulphuric acid. The hydrogen bromide is formed under situ (in place). The hydrogen bromide then reacts with the alcohol to form a haloalkane.