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Carboxylic Acids
AQA A Level Chemistry
Question | Answer |
---|---|
Draw the functional group of a carboxylic acid | |
draw 3-methylbutanoic acid | |
What is the strongest intermolecular force between Carboxylic acids | Hydrogen bonding |
Why are carboxylic acids soluble in water | they can form hydrogen bonds between the acid and water |
Draw the hydrogen bond between water and ethanoic acid | |
Describe how a carboxylic acid is produced from an alcohol | Heat a primary alcohol with potassium dichromate under reflux |
Write the chemical reaction between Propanoic acid and sodium carbonate | CH3CH3COO + Na2CO3 --> CH3CH3COONa + H2O + CO2 |
Draw the functional group of a carboxylic acid | |
draw 3-methylbutanoic acid | |
What is the strongest intermolecular force between Carboxylic acids | Hydrogen bonding |
Why are carboxylic acids soluble in water | they can form hydrogen bonds between the acid and water |
Draw the hydrogen bond between water and ethanoic acid | |
Describe how a carboxylic acid is produced from an alcohol | Heat a primary alcohol with potassium dichromate under reflux |
Write the chemical reaction between Propanoic acid and sodium carbonate | CH3CH3COO + Na2CO3 --> CH3CH3COONa + H2O + CO2 |
What are the reagents and conditions required to reduce a carboxylic acid | Heat under reflux with LiAlH4 in dry ether |
What are the products formed when ethanoic acid is reacted with phosphorus (V) chloride | Ethanoyl chloride, POCl3 and HCl |
How is 2-hydoxypropanoic acid is formed from 2-hydroxypropanitrile | hydrolysis, reflux with water and H+ ions |
What are the reagents and conditions required to convert a carboxylic acid into an ester | Heat under reflux with an alcohol and conc sulfuric acid |
Name the mechnanism for formation of an ester | Nucleophillic addition-elmination |
Write the reaction and name of the ester when propanoic acid and ethanol | Reaction: name: ethly propanoate |
Draw the mechanism for the reaction between ethanol and propanoic acid | |
Draw the structure of ethanoic anhydride | |
Draw the structure of propanoyl chloride | |
Write the reaction between ethanoic anhydride and methanol | |
Draw the mechanism between methanoic anhydride and ethanol | |
Write the reaction for the hydrolysis of methyl ethanoate in acidic conditions | |
Write the reaction of hydrolysis of methyl ethanoate in alkaline conditions | |
How is a triglyceride converted into a soap molecule | heat the tricglyceride with NaOH to hydrolyse the ester |
How is a triglyceride converted into a biodiesel molecule | heat the triclyceride with methanol to hyrdrolyse the ester to a smaller ester molecule |
List three advantages of biodiesel | Renewable, biodegradable, carbon neutral, non toxic, simple to make etc |
List 2 disadvantage of biodiesel | Poor availabilty, more expensive, can cause engine problems, takes up land |
Why are Acyl chlorides more reactive than carboxyic acids | The electronegative chlorine atom pulls electrons toward it in the C-Cl bond, which makes the carbonyl carbon more electrophilic. |
What conditions and reagents are required to turn an acyl chloride into an ester? | If you add an acyl chloride to an alcohol, you get a vigorous (even violent) reaction at room temperature |
Draw the mechanism for the reaction between propanoyl chloride and methanol. |