Six original Cambridge-style questions on esters.
Ethanoic acid is warmed with propan-1-ol and a few drops of concentrated sulfuric acid. Write the equation, name the ester and state the role of the sulfuric acid.
Give the names of the carboxylic acid and the alcohol needed to make (a) methyl butanoate, (b) ethyl methanoate, HCOOC2H5.
Compare the hydrolysis of methyl ethanoate by dilute sulfuric acid and by aqueous sodium hydroxide. Give the products of each and explain why only one goes to completion.
6.00 g of ethanoic acid (Mr 60.0) is heated with excess ethanol and concentrated sulfuric acid. 5.72 g of ethyl ethanoate (Mr 88.0) is obtained. Calculate the percentage yield and suggest why it is below 100%.
17.8 g of glyceryl tristearate (Mr 890) is boiled with excess NaOH(aq). Write a word equation and calculate the mass of NaOH used and the mass of sodium stearate (Mr 306) formed.
State two uses of esters and explain why unsaturated oils are liquids at room temperature while saturated fats are solids.
Mark this once you have attempted all six and checked your working. It records a Practiced badge on the topic and adds a one-time bonus. Revealing the solutions alone does not count.