Chapter Five · Organic chemistry · Chemistry. These are 10 questions from the Magmo3 bank on this lesson, from easy to hard. Solve each one, then open "Show answer and explanation". Magmo3 has 46 questions on this lesson, each with an explanation.
Esters are widely used in the food and perfume industries mainly because they:
AGive a silver mirror with Tollens' reagent
BReact vigorously with carbonates
CHave pleasant fruity odours
DAre strong acids
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Correct answer: (C) Have pleasant fruity odours
Explanation: Esters have characteristic sweet, fruity smells, so they are used as flavourings and in perfumes.
Question 2Easy
The reaction between ethanoic acid and methanol produces which ester?
AMethyl ethanoate
BMethyl methanoate
CEthyl methanoate
DEthyl ethanoate
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Correct answer: (A) Methyl ethanoate
Explanation: The alcohol supplies the alkyl group (methyl) and the acid supplies the acyl group (ethanoate), giving methyl ethanoate.
Question 3Easy
What is the chemical name of Aspirin?
AAscorbic acid
BTrinitrotoluene
CAcetylsalicylic acid
DPolynil chloride
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Correct answer: (C) Acetylsalicylic acid
Explanation: Aspirin is well-known as acetylsalicylic acid in the context of organic derivatives.
Question 4Medium
Which of the following describes the nature of ester odor as the molecular mass of the constituent alcohol and acid increases?
AThe odor decreases, and the state changes toward a waxy solid.
BThe odor becomes more pungent and intense.
CThe odor shifts from fruity to medicinal.
DThe odor remains constant regardless of molecular mass.
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Correct answer: (A) The odor decreases, and the state changes toward a waxy solid.
Explanation: The odor of the ester decreases by the increase of the molecular mass of the alcohol and acid used, turning into a waxy solid.
Question 5Medium
Which statement correctly compares the acidic hydrolysis of an ester with its alkaline hydrolysis (heating with aqueous NaOH)?
ABoth give exactly the same products
BAcidic hydrolysis gives the sodium salt of the acid and an alcohol, while alkaline hydrolysis gives the carboxylic acid and an alcohol
CAcidic hydrolysis gives an alcohol only, while alkaline hydrolysis gives a carboxylic acid only
DAcidic hydrolysis gives the carboxylic acid and the alcohol, while alkaline hydrolysis gives the salt of the acid and the alcohol
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Correct answer: (D) Acidic hydrolysis gives the carboxylic acid and the alcohol, while alkaline hydrolysis gives the salt of the acid and the alcohol
Explanation: Acid hydrolysis, catalysed by a dilute mineral acid, is the reverse of esterification and gives the carboxylic acid and the alcohol, e.g. acetic acid and ethanol. Alkaline hydrolysis (saponification) with aqueous NaOH gives the salt of the acid and the alcohol, e.g. sodium acetate and ethanol.
Question 6Medium
Three liquids are tested: A is neutral to litmus and turns acidified potassium dichromate from orange to green, B gives effervescence with sodium carbonate, and C has a pleasant fruity smell. Compounds A, B and C respectively are:
AAn ester, a primary alcohol, a carboxylic acid
BA primary alcohol, a carboxylic acid, an ester
CA carboxylic acid, an ester, a primary alcohol
DA tertiary alcohol, a carboxylic acid, an ester
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Correct answer: (B) A primary alcohol, a carboxylic acid, an ester
Explanation: A is a primary alcohol: alcohols are neutral to litmus and a primary alcohol is oxidised by acidified dichromate (orange to green), whereas a tertiary alcohol is not. B releases CO₂ from a carbonate, so it is a carboxylic acid, and C, with a pleasant fruity smell, is an ester.
Question 7Medium
What is the result of the ammonolysis of ethyl benzoate?
ABenzamide and ethanol.
BAcetamide and ethanol.
CEthyl acetate and ammonia.
DBenzoic acid and ethylamine.
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Correct answer: (A) Benzamide and ethanol.
Explanation: Ammonolysis of esters gives acid amide and the alcohol; specifically, ethyl benzoate reacts with ammonia to give benzamide and ethanol.
Question 8Hard
The carboxylic acid ethanoic acid is isomeric with which ester of the same molecular formula (C2H4O2)?
AEthyl ethanoate
BMethyl methanoate
CEthyl methanoate
DMethyl ethanoate
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Correct answer: (B) Methyl methanoate
Explanation: Ethanoic acid (CH3COOH) and methyl methanoate (HCOOCH3) are isomers, both having the molecular formula C2H4O2.
Question 9Hard
What is the correct structural characteristic when comparing methyl acetate and methyl formate's classification tables?
ABoth belong to the carboxylic acid salt category.
BBoth are classified as esters, but have different total numbers of carbon atoms.
CBoth take names strictly according to inorganic nomenclature.
DBoth yield identical products upon complete reduction.
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Correct answer: (B) Both are classified as esters, but have different total numbers of carbon atoms.
Explanation: Both methyl acetate and methyl formate are listed under esters, differing in their alkyl and acid-derived carbon chain lengths.
Question 10Hard
Which of the following sets contains exclusively compounds classified as esters according to the provided text tables?
AMethyl acetate, Sodium acetate, Ethanoic acid, Vitamin C
Explanation: Aspirin, CH3COOC6H5 (phenyl acetate), C6H5COOCH3 (methyl benzoate), and Dacron are all explicitly categorized or contain ester functional groups as per the tables.