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
Alcohols and Phenols
Reactions of primary and secondary alcohols
- 3 things to know
- A2 Unit 4
Overview
Recall questions on Reactions of primary and secondary alcohols.
What you need to know
Answer each one before you reveal it.
Place primary, secondary and tertiary alcohols in order of how readily they react with hydrogen halides.
What extra reagent helps a primary alcohol react with hydrochloric acid, in what order do the classes of alcohol react, and what forms when a primary alcohol meets ethanoyl chloride?
Questions from this subtopic
Each one with the model answer underneath.
- 1
What type of compound is formed when an alcohol reacts with a hydrogen halide?
Model answer
A halogenoalkane, together with water. The hydroxyl group is replaced by the halogen atom, so ethanol and hydrogen bromide give bromoethane.
- 2
Write the equation for the reaction of ethanol with hydrogen bromide.
Model answer
C₂H₅OH + HBr → C₂H₅Br + H₂O. The product is bromoethane and the reaction is a substitution.
- 3
How is the hydrogen bromide usually supplied when a bromoalkane is prepared from an alcohol?
Model answer
It is generated in the flask by warming sodium bromide with concentrated sulfuric acid, NaBr + H₂SO₄ → NaHSO₄ + HBr, and the alcohol is present so that the hydrogen bromide reacts as it forms. The mixture is then heated under reflux.
- 4
Why is concentrated phosphoric acid, rather than concentrated sulfuric acid, used with potassium iodide to make an iodoalkane?
Model answer
Concentrated sulfuric acid is a strong enough oxidising agent to oxidise iodide ions to iodine, so much of the halide would be destroyed before it could form hydrogen iodide. Phosphoric acid is not an oxidising agent, so it liberates hydrogen iodide cleanly.
- 5
What extra reagent helps a primary alcohol react with concentrated hydrochloric acid?
Model answer
Anhydrous zinc chloride is added as a catalyst, and the mixture is warmed. Without it a primary alcohol reacts only very slowly with hydrogen chloride, whereas a tertiary alcohol reacts on shaking at room temperature.
- 6
Place primary, secondary and tertiary alcohols in order of how readily they react with hydrogen halides.
Model answer
Tertiary reacts fastest, then secondary, then primary. The reaction proceeds most easily when the carbon bearing the hydroxyl group can support a positive charge, and alkyl groups attached to that carbon release electron density towards it, so more alkyl groups make substitution easier.
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