OCR A-Level Chemistry H432
Foundations in Chemistry
Bonding and Structure
Periodic Table and Energy
Enthalpy Changes
Chemical Equilibrium
Basic Concepts of Organic Chemistry
Core Organic Chemistry
Alkenes
Organic Synthesis
How Fast?
Physical Chemistry and Transition Elements
Acids, Bases and Buffers
Redox and Electrode Potentials
Transition Elements
Aromatic Compounds
Organic Chemistry and Analysis
Spectroscopy
Organic Synthesis
Esters, acyl chlorides, condensation polymers and racemic mixtures
- 4 things to know
- Components 02 and 03
Overview
Recall questions on forming an ester and an acyl chloride, the products with amines and alcohols, the monomers of polyesters and polyamides, and why HCN addition gives a racemic mixture.
What you need to know
Answer each one before you reveal it.
What product forms when an acyl chloride reacts with an amine?
What is produced when an acyl chloride reacts with an alcohol?
Why does nucleophilic addition of HCN to an aldehyde produce a racemic mixture?
Questions from this subtopic
Each one with the model answer underneath.
- 1
What reagent reacts with a carboxylic acid to form an ester?
Model answer
An alcohol (in the presence of an acid catalyst).
- 2
Name a reagent that converts a carboxylic acid into an acyl chloride.
Model answer
SOCl₂ (thionyl chloride) or PCl₅ (phosphorus pentachloride).
- 3
What product forms when an acyl chloride reacts with an amine?
Model answer
An amide (and HCl).
- 4
What is produced when an acyl chloride reacts with an alcohol?
Model answer
An ester (and HCl).
- 5
Why might the order of steps in a synthetic route be important?
Model answer
To protect certain functional groups from unwanted reactions or to ensure selectivity of reactions.
- 6
What monomers undergo condensation polymerisation to form a polyester?
Model answer
A dicarboxylic acid and a diol.
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