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3. The displayed formula for carboxylic acid A is:
The name of carboxylic acid A is ...
4.The name of the gas formed in this reaction is ...
7. The approximate pH of ethanoic acid is ...
Q9-10: Polyesters such as terylene are formed by the reaction between a dicarboxylic acid with a diol. Polyesters are condensation polymers.
10. Block diagrams of monomer A (a dicarboxylic acid) and monomer B (a diol) are:
The repeating unit of the polymer formed from these monomers is:
Question 1:
The correct answer is D. –COOH.
The functional group of carboxylic acids is the carboxyl group, written as –COOH (carbon double-bonded to oxygen and single-bonded to a hydroxyl group).
A. C=C — Alkene functional group.
B. –O–H — Hydroxyl group (alcohols/phenols).
C. –COO– — Ester group (ester linkage, not carboxylic acid).
D. –COOH — Correct for carboxylic acids.
*These A.I. responses have been individually checked to ensure they match the accepted answer, but explanations may still be incorrect. Responses may give guidance but the A.I. might not be able to answer the question! This is particularly the case for questions based on diagrams, which the A.I. typically cannot interpret. Grade Gorilla uses Gemini, Deepseek and a range of other A.I. chatbots to generate the saved responses. Some answers have had human intervention for clarity or where the A.I. has not been able to answer the question.
Question 2:
The correct answer is A. oxidation.
When ethanol (C₂H₅OH) is exposed to microbes (e.g., Acetobacter bacteria) in the air, it is oxidized to ethanoic acid (CH₃COOH). This process is sometimes called the second stage of fermentation (where alcohol is further oxidized to vinegar), but chemically it is an oxidation reaction.
B. reduction — Opposite process (gain of electrons/hydrogen).
C. fermentation — Usually refers to sugar → ethanol (anaerobic), not ethanol → ethanoic acid.
D. esterification — Reaction between an alcohol and a carboxylic acid to form an ester.
Question 3:
The name of carboxylic acid A is propanoic acid (Option B).
Reasoning:
Identify the carbon chain:
Count the total number of carbon atoms in the longest chain that includes the functional group. In this molecule, there are 3 carbon atoms.
Determine the prefix:
Identify the functional group:
The group -COOH (a carbon double-bonded to an oxygen and single-bonded to an -OH group) confirms it is a carboxylic acid, which uses the suffix -anoic acid.
Combine: Prop- + -anoic acid = propanoic acid.
Question 4:
The correct answer is C. hydrogen.
Ethanoic acid (CH₃COOH) reacts with magnesium metal in a typical acid-metal reaction:
2CH₃COOH + Mg → (CH₃COO)₂Mg + H₂↑
The gas produced is hydrogen, which can be tested for by using a lighted splint (pops).
A. Carbon dioxide — Produced when carbonates or bicarbonates react with acids.
B. Oxygen — Not produced in this reaction.
D. Ethane — Not formed here.
Question 5:
The correct answer is A. magnesium ethanoate.
When ethanoic acid (CH₃COOH) reacts with magnesium metal, the hydrogen atom in the carboxyl group is replaced by magnesium ions, forming the salt magnesium ethanoate, with the formula (CH₃COO)₂Mg.
B. magnesium ethanoic — Incorrect; "ethanoic" refers to the acid, not the salt.
C. magnesium ethanide — Incorrect; "ethanide" suggests a carbanion compound (e.g., C₂H₅⁻), not a carboxylate salt.
D. magnesium ethoate — Incorrect; not the standard IUPAC name.
Question 6:
The correct answer is C. carbon dioxide and water.
When a carboxylic acid (e.g., ethanoic acid) reacts with sodium carbonate, the products are a salt, carbon dioxide, and water:
2CH₃COOH + Na₂CO₃ → 2CH₃COONa + CO₂↑ + H₂O
A. hydrogen only — Incorrect (this is produced with reactive metals like Mg, not carbonates).
B. water only — Incomplete; carbon dioxide is also produced.
C. carbon dioxide and water — Correct.
D. carbon dioxide and hydrogen — Incorrect (hydrogen is not produced here).
Question 7:
The correct answer is B. pH 5.
Ethanoic acid (acetic acid, CH₃COOH) is a weak acid, which means it only partially dissociates in water. A 0.1 M solution of ethanoic acid has a pH of approximately 2.9, but in more general terms (depending on concentration and common teaching examples), the pH of dilute ethanoic acid is often stated as around 3–5.
Given the options:
A. pH 1 — Strong acid like hydrochloric acid (0.1 M).
B. pH 5 — Typical for a dilute weak carboxylic acid.
C. pH 9 — Weak base (e.g., sodium hydrogen carbonate).
D. pH 13 — Strong base (e.g., sodium hydroxide).
Question 8:
The correct answer is B. an ester.
When ethanoic acid (CH₃COOH) reacts with ethanol (C₂H₅OH) in the presence of an acid catalyst (e.g., concentrated H₂SO₄), an esterification reaction occurs, producing an ester (ethyl ethanoate, CH₃COOC₂H₅) and water:
CH₃COOH + C₂H₅OH ⇌ CH₃COOC₂H₅ + H₂O
A. a salt — Formed from acid + base or acid + metal/carbonate, not acid + alcohol.
C. a polymer — Not from simple esterification of two small molecules.
D. a sugar — Carbohydrates, unrelated here.
Question 9:
The correct answer is D. water is also formed.
A condensation polymer is formed when monomers join together with the loss of a small molecule, such as water (or sometimes methanol, HCl, etc.).
In the case of polyesters like Terylene:
A dicarboxylic acid reacts with a diol.
Each ester bond forms with the elimination of a water molecule.
Checking the options:
A. gas turns into liquid — Not relevant to the definition.
B. only one product is formed — False; the polymer and water are formed.
C. a long chain molecule is formed — True of all polymers, not specific to condensation polymers.
D. water is also formed — Correct; the defining feature of condensation polymerization in this case.
Question 10:
Based on the chemical reaction between a dicarboxilic acid (Monomer A) and a diol (Monomer B), the correct repeating unit is C.
Reasoning
Condensation Polymerization:
When these two monomers react to form a polyester, a molecule of water H₂O is removed at each linkage point.
The -OH group is lost from the carboxylic acid.
The -H atom is lost from the alcohol group.
The Linkage:
This creates an ester link -COO- connecting the block (A) and the circle (B).
The Repeating Unit:
A repeating unit shows the structure that repeats infinitely. Therefore, it should not have the terminal -H or -OH groups shown in options A and B (those are for the monomers or the end-groups of the whole chain).
Option C correctly shows the unit with the bonds extending out from the carbonyl carbon and the oxygen atom, ready to connect to the next unit.
Correct Answer: C