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Card 6
Front
Why are racemic mixtures optically inactive?
Back
Card 7
Front
How could you practically tell the difference between enantiomers of an optical isomer?
Back
Card 8
Front
Can aldehydes be oxidised? Can ketones? What products do they form?
Back
Card 9
Front
Describe the chemical tests to distinguish between aldehydes and ketones. What would you observe?
Back
Card 10
Front
Aldehydes and ketones can be reduced . Give the reagent, used in aquaous solution, which reduces them.
Back
Card 11
Front
What type of mechanism is used to show the reduction of aldehydes and ketones?
Back
Card 12
Front
Describe the hazards of using KCN
Back
Card 13
Front
What would you observe on adding carboxylic acid to a carbonate. Why?
Back
Card 14
Front
Carboxylic acids are desrcibed as weak acids. Why?
Back
Card 15
Front
How can esters be produced?
Back
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