Benzoic acid can be formed from the oxidation of methylbenzene.
Draw the displayed formula of benzoic acid.
[3]
[2]
Write an equation to show that benzoic acid acts as a weak acid.
Did this page help you?
Benzoic acid can be formed from the oxidation of methylbenzene.
Draw the displayed formula of benzoic acid.
How did you do?
[3]
[2]
How did you do?
Write an equation to show that benzoic acid acts as a weak acid.
How did you do?
Did this page help you?
Benzoic acid can be formed from methylbenzene.
This process occurs in two stages.
methylbenzene potassium benzoate benzoic acid
How did you do?
How did you do?
Describe the observations that could be made during step 1.
How did you do?
Describe and explain the relative acidities of benzoic acid and phenol.
How did you do?
Did this page help you?
Fig. 2.1 shows three different molecules.
Fig. 2.1
Propan-1-ol can react with sodium metal.
Write an equation for this reaction.
How did you do?
How did you do?
Another carboxylic acid, methanoic acid is similar to propanoic acid in terms of its acidity.
How did you do?
Did this page help you?
The acyl chloride, ethanedioyl dichloride is shown in Fig. 3.1.
This can be synthesised from compound X in a single step.
Fig. 3.1
Suggest the identify of compound X.
How did you do?
State the reagents and conditions needed to convert X into ClCOCOCl.
How did you do?
A different acyl chloride was used to synthesize ethyl butanoate.
How did you do?
Did this page help you?
Describe and explain the relative acidities of benzoic acid, phenylmethanol and 4-methylphenol shown in Fig. 1.1.
Fig. 1.1
How did you do?
The ester 4-methylphenyl benzoate is used in the manufacture of perfumes and can be formed in two steps from two of the compounds shown in Fig. 1.1 in part (a).
How did you do?
State the reagents and conditions required to form benzoic acid from methylbenzene.
How did you do?
Did this page help you?