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Edexcel IAL Chemistry 20.2 Grignard reagents and chain extension

Choose the organomagnesium halide from the product: Grignard reagents act as nucleophiles, then hydrolysis gives alcohols or carboxylic acids.

Syllabus
First assessment 2019
Course
Chemistry YCH11
Level
A2

Exam points

  • Select magnesium and dry ether to form a Grignard reagent from a halogenoalkane.
  • Predict alcohol or carboxylic acid products after reaction with carbonyl compounds or CO2.
  • Choose the Grignard reagent and carbonyl partner needed for a target alcohol.

20.2—Methods of increasing the length of the carbon chain in a molecule by the use of magnesium to form Grignard reagents and question 1

[Maximum number: 6]

Benzoic acid is a white crystalline solid with the structure shown.

Figure for Question 20.2—Methods of increasing the length of the carbon chain in a molecule by the use of magnesium to form Grignard reagents and question 1 — Edexcel A-Level Chemistry A2

It is found in many plants as it is an important building block for the biosynthesis of a variety of compounds, such as plant hormones and attractants for pollinators.

The role of benzoic acid in the chemical industry is also widespread and approximately 500000 tonnes are produced annually. It is used in the synthesis of many compounds, including medicines, dyes and insect repellents.

Such synthetic dyes are often classified as aryl azo dyes. These dyes have a range of vivid colours and a wide range of uses in many industries, including food and textiles. Their synthesis involves the formation of a diazonium ion. This ion then reacts with a phenol in a coupling reaction, to form the dye. The relative simplicity of the reactions involved and ready availability of starting materials make azo dyes cheap to produce.

Salts of benzoic acid, such as calcium benzoate and sodium benzoate, are used in the food industry as preservatives.

Devise a reaction scheme to produce benzoic acid from benzene, via bromobenzene and then a Grignard reagent.

Include the reagents and essential conditions for each step and give the name or structure of each of the intermediate compounds.

Details of practical procedures and reaction mechanisms are not required.

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