Alcohols Flashcards
What are primary alcohols?
One carbon is attached to the carbon that has a hydroxyl group attached to it.
What are secondary alcohols?
Two carbons are attached to the carbon that has a hydroxyl group attached to it.
What are tertiary alcohols?
Three carbons are attached to the carbon that has a hydroxyl group attached to it.
What is the mechanism for the dehydration of an alcohol to make an alkene?
elimination
What conditions are needed for the dehydration of alcohols to make alkenes?
The alcohol is heated under reflux with concentrated sulfuric acid.
Name and outline the mechanism for the dehydration of propane-2-ol using sulfuric acid.
What are the products of the partial oxidation of primary alcohols?
aldehydes
What conditions are needed for the partial oxidation of alcohols?
- potassium dichromate
- dilute sulfuric acid
- warm gently and distil the products out as they are made
What are the products of the full oxidation of primary alcohols?
a carboxylic acid
What conditions are needed for the full oxidation of alcohols?
- an excess of potassium dichromate
- dilute sulfuric acid
- heat under reflux and distil the product after the reaction has finished
What are the products of the oxidation of secondary alcohols?
a ketone
What conditions are needed for the oxidation of secondary alcohols?
- Potassium dichromate and dilute sulfuric acid.
- Heat under reflux
How does potassium dichromate oxidise the alcohols?
The orange dichromate ion is reduced to a green chromium 3+ ion and this oxidises the alcohols.
How is Tollen’s reagent used to test for aldehydes and ketones?
In the presence of an aldehyde, a silver mirror will form and in the presence of a ketone, there will be no change.
What is Tollen’s reagent made out of?
aqueous ammonia and silver nitrate to form a complex ion. [Ag(NH3)2]+
How does Tollen’s reagent work?
The silver ions are reduced to silver atoms and this causes the aldehydes to be reduced into carboxylic acids.
How is Fehling’s solution used to test for aldehydes and ketones?
In the presence of an aldehyde, the blue solution will turn into a red precipitate.
What is Fehling’s solution made out of?
Cu 2+ ions
How does Fehling’s solution work?
The blue copper ions are reduced to form a red precipitate and the aldehydes are reduced into a carboxylic acid.
How do you test for a carboxylic acid?
You add sodium carbonate and there will be fizzing as CO2 is produced.
Why is there no reaction with the ketones?
The functional group does not contain hydrogen so the ketones can’t be oxidised.
Write the equation for the production of ethanol from the fermentation of glucose.
What conditions are needed for fermentation?
- Yeast
- No air
- Temperatures of 30 to 40 degrees
Why do the conditions need to be anaerobic?
So the ethanol isn’t oxidised into ethanoic acid.
What are the advantages of fermentation?
- Sugar is renewable
- relatively cheap
What are the disadvantages of fermentation?
- the ethanol produced is not pure and needs to be purified
- this is a batch process which is slow and expensive
- uses land that could be used to grow crops
Write the equation for the production of ethanol from ethene and steam.
What conditions are needed for the hydration of ethene?
- high temperatures of 300 degrees
- high pressure of 70 atm
- strong acid catalyst
What are the advantages of the hydration of ethene?
- the product made is pure
- continuous process meaning that less manpower is needed to keep it going
What are the disadvantages of the hydration of ethene?
- ethene is not a renewable resource
- expensive equipment needed
- expensive to maintain high pressures
Why can the use of ethanol as a biofuel be considered carbon neutral?
6 carbon molecules are taken in for photosynthesis and the production of glucose and 6 molecules of carbon dioxide are released in the combustion of ethanol. This means there is no net contribution to carbon dioxide emissions.
Why might the use of ethanol as a biofuel not be considered carbon neutral?
Carbon dioxide is released when plants are watered, transportation and distilling the impure product.