Achieved question Flashcards
to grasp the achieved concepts
what substance will oxidise a secondary alcohol?
Acidified potassium permangante or acidified potassium dichromate
what is the colour of potassium permangante
purple
what is a chiral carbon?
a carbon atom bonded to 4 different groups or atoms
give 4 characteristics of optical isomers
- They rotate the plane of polarised light the same amount in different directions
- They react differently with other optical isomers
- They are mirror images of each other
- They have the same physical and chemical properties
Name the 3 compounds that can be used to distinguish an aldehyde from a primary or secondary alcohol?
Why can they be used?
Fehlings,Benedicts and Tollens reagents
They can be used because they are weak oxidising agents only strong enough to oxidise an aldehyde and not alcohols
When Tollens oxidises an aldehyde what do you see?
A silver mirror
What organic product is formed when a benedicts oxidises ethanal?
ethanoic acid
butanal can be reduced to butan-1-ol by what compound?
sodium borohydride
How would you collect an aldehyde when oxidising a primary alcohol?
use a distillation appartus
How could you determine an alcohol from an amine and what would you observe?
put red litmus paper in both solutions. The litmus in the alcohol will stay red where the amine will turn it blue
Name the ester made from ethanol and propanoic acid
ethylpropanoate
What conditions are required to make an ester from an alcohol and carboxylic acid?
concentrated sulfuric acid and heat
How can you make an amine from a haloalkane?
Add alcoholic ammonia
To hydrolyse (break apart) an ester you can use 2 different conditions - what are they?
Acidic or basic conditions
Hydrolysing an ester in acid condtions forms what 2 products?
an alcohol and carboxylic acid
Hydrolysing an ester in basic conditions (eg in NaOH) forms what 2 products?
an alcohol and the salt of the carboxylic acid