Eduqas A-Level Chemistry A410QS
Formulae and Equations
Basic Ideas About Atoms
Chemical Calculations
Bonding
Solid Structures
The Periodic Table
Simple Equilibria and Acid-Base Reactions
Thermochemistry
Rates of Reaction
The Wider Impact of Chemistry
Organic Compounds
Hydrocarbons
Halogenoalkanes
Alcohols and Carboxylic Acids
Instrumental Analysis
Redox and Standard Electrode Potential
Redox Reactions
Chemistry of the P-Block
Chemistry of the D-Block Transition Metals
Chemical Kinetics
Enthalpy Changes for Solids and Solutions
Entropy and Feasibility of Reactions
Equilibrium Constants
Acid-Base Equilibria
Stereoisomerism
Aromaticity
Alcohols and Phenols
Aldehydes and Ketones
Carboxylic Acids and Their Derivatives
Amines
Amino Acids, Peptides and Proteins
Organic Synthesis and Analysis
Specified Practical Work
Practical Skills and Techniques
Mathematical Skills in Chemistry
Specified Practical Work
Hydrolysis of 1-bromobutane and the preparation of an ester
- 3 things to know
- Component 3
Overview
Recall questions on the reflux apparatus and the reagents for the hydrolysis, the co-solvent problem and why ethanol is added, the preparation of an ester and its separation by distillation, the washing and drying steps, and the yield calculation.
What you need to know
Answer each one before you reveal it.
Why is ethanol added to the mixture when 1-bromobutane is hydrolysed by aqueous sodium hydroxide?
Why must the top of a reflux condenser be left open to the atmosphere?
Questions from this subtopic
Each one with the model answer underneath.
- 1
Why is 1-bromobutane heated under reflux with aqueous sodium hydroxide rather than simply warmed in an open flask?
Model answer
1-bromobutane boils at about 102 °C and would evaporate away before the slow hydrolysis was complete, whereas reflux condenses the vapour and returns it so the mixture can be held at its boiling temperature for as long as is needed.
- 2
Why is ethanol added to the mixture when 1-bromobutane is hydrolysed by aqueous sodium hydroxide?
Model answer
The halogenoalkane and the aqueous alkali do not mix, so the reaction would be confined to the interface. Ethanol dissolves both and gives a single phase in which the reagents can meet throughout the solution.
- 3
Why is an electric heater or a water bath used rather than a Bunsen burner in this preparation?
Model answer
Both the halogenoalkane and the ethanol give off flammable vapour, and a naked flame near the top of the condenser could ignite it.
- 4
What is the purpose of the anti-bumping granules added to the flask?
Model answer
Their rough surfaces give sites where small bubbles form steadily, so the liquid boils smoothly instead of superheating and then erupting in a large bubble.
- 5
Why is the cooling water fed into the bottom of the condenser jacket?
Model answer
Filling against gravity keeps the jacket full of water at all times and sets up a counter-current to the rising vapour, so the coldest water meets the vapour that has travelled furthest up the tube.
- 6
Why must the top of a reflux condenser be left open to the atmosphere?
Model answer
A closed apparatus containing boiling liquid builds up pressure as the vapour expands and the glassware could be forced apart or burst.
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