HARD
AS and A Level
IMPORTANT
Earn 100

Propan-1-ol can be oxidised to propanal, CH3CH2CHO, and then to propanoic acid, CH3CH2COOH.

Write a balanced chemical equation for the oxidation of propan-1-ol to propanal. Oxygen from the oxidising agent should be shown as [O].

Important Questions on Alcohols, Esters and Carboxylic Acids

EASY
AS and A Level
IMPORTANT

Propan-1-ol can be oxidised to propanal, CH3CH2CHO, and then to propanoic acid, CH3CH2COOH.

What reagents and conditions should be used to oxidise propan-1-ol to propanoic acid?

HARD
AS and A Level
IMPORTANT

Propan-1-ol can be oxidised to propanal, CH3CH2CHO, and then to propanoic acid, CH3CH2COOH.

Write a balanced chemical equation for the oxidation of propan-1-ol to propanoic acid. Oxygen from the oxidising agent should be shown as [O].

MEDIUM
AS and A Level
IMPORTANT
Name and give the formula of the reducing agent used to convert carboxylic acids to primary alcohols.
EASY
AS and A Level
IMPORTANT

Write a balanced chemical equation for  the following process. Structural or displayed formulae should be used for all organic substances.

Making ethanol using ethene as feedstock. Include the formula of the catalyst used.      

MEDIUM
AS and A Level
IMPORTANT

Write a balanced chemical equation for the following process. Structural or displayed formulae should be used for all organic substances.

The complete combustion of ethanol in oxygen.             

MEDIUM
AS and A Level
IMPORTANT

Write a balanced chemical equation for the following process. Structural or displayed formulae should be used for all organic substances.

The reaction of ethanoic acid with ethanol. Name the catalyst used, the type of reaction, and the products.       

EASY
AS and A Level
IMPORTANT

Primary and secondary alcohols can be oxidised by heating with a mixture of potassium dichromate(VI) and dilute sulfuric(VI) acid.
■ A primary alcohol can be oxidised to two different products, depending on the conditions used.
■ A secondary alcohol forms one product when oxidised.
■ Tertiary alcohols cannot be oxidised.

Why are tertiary alcohols resistant to oxidation?