WJEC A-Level Chemistry 1410QS
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
Practical Skills and Techniques
Planning, Analysis and Evaluation
Core Experiments and Their Chemistry
Mathematical Skills in Chemistry
Carboxylic Acids and Their Derivatives
Reduction and decarboxylation of carboxylic acids: decarboxylation of carboxylic acids
- 3 things to know
- A2 Unit 4
Overview
Recall questions on decarboxylation.
What you need to know
Answer each one before you reveal it.
An unknown sodium carboxylate is heated with soda lime and the gas produced is butane. What was the original acid?
Which reducing agent would you choose to convert butanoic acid into butan-1-ol, and which to convert butanal into butan-1-ol?
Questions from this subtopic
Each one with the model answer underneath.
- 1
Which reducing agent would you choose to convert butanoic acid into butan-1-ol, and which to convert butanal into butan-1-ol?
Model answer
For butanoic acid only lithium tetrahydridoaluminate(III) in dry ether is powerful enough. For butanal either reagent works, and sodium tetrahydridoborate(III) in aqueous or alcoholic solution would be the simpler and safer choice.
- 2
What is meant by decarboxylation?
Model answer
It is the removal of the carboxyl group from a carboxylic acid as carbon dioxide, leaving a product with one carbon atom fewer. The carbon dioxide is retained as a carbonate when the reaction is carried out in alkali.
- 3
What reagent and conditions bring about the decarboxylation of a carboxylic acid?
Model answer
The sodium salt of the acid is heated strongly with soda lime, which is a solid mixture of sodium hydroxide and calcium oxide. The alkane leaves as a gas or vapour and sodium carbonate is left in the tube.
- 4
Write an equation for the reaction of sodium ethanoate with sodium hydroxide on heating with soda lime.
Model answer
The equation is CH₃COONa + NaOH → CH₄ + Na₂CO₃. Methane is given off and sodium carbonate remains.
- 5
Why is calcium oxide included in soda lime rather than using sodium hydroxide alone?
Model answer
Solid sodium hydroxide is deliquescent and melts to a corrosive liquid when heated, which attacks the glassware and is difficult to handle. Mixing it with calcium oxide gives a dry, granular solid that stays porous and can be heated strongly in a tube.
- 6
What is produced when sodium propanoate is heated with soda lime?
Model answer
Ethane is produced, together with sodium carbonate: CH₃CH₂COONa + NaOH → CH₃CH₃ + Na₂CO₃. The three-carbon salt gives a two-carbon alkane.
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