OCR A-Level Chemistry B H433
Development of Practical Skills in Chemistry
Elements of Life
Developing Fuels
Elements From the Sea
The Ozone Story
What's in a Medicine?
The Chemical Industry
Polymers and Life
Oceans
Developing Metals
Colour by Design
Chemical Literacy
Mathematical Skills in Chemistry
Colour by Design
Cyanohydrin formation and its use in synthesis
- 1 thing to know
- Components 01, 02 and 03
Overview
Recall questions on the reagent, the product and its class, why the reaction is useful for lengthening a chain, and the safety precaution.
What you need to know
Answer each one before you reveal it.
Questions from this subtopic
Each one with the model answer underneath.
- 1
Explain how the three carbonyl tests work together to place an unknown compound.
Model answer
Acidified dichromate shows whether the compound can be oxidised at all, while Tollens' and Fehling's are mild enough to be positive only for an aldehyde, so together they separate aldehydes from ketones and from alcohols.
- 2
Which reagent converts a carbonyl compound into a cyanohydrin?
Model answer
Hydrogen cyanide, usually generated in situ from potassium or sodium cyanide with a little acid, so that cyanide ions remain available to attack.
- 3
What is the systematic class name for a cyanohydrin?
Model answer
It is a hydroxynitrile.
- 4
Give the formula of the product formed when ethanal reacts with hydrogen cyanide.
Model answer
The product is CH₃CH(OH)CN.
- 5
Name the product formed when ethanal reacts with hydrogen cyanide.
Model answer
It is 2-hydroxypropanenitrile.
- 6
Give the formula of the product formed when propanone reacts with hydrogen cyanide.
Model answer
The product is (CH₃)₂C(OH)CN.
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