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ACSEE (Form 6) Chemical Bonding — practice questions

Explore 10 free Chemical Bonding questions in ACSEE (Form 6) Chemistry. Open each question or exercise to read its content, reference answers and available explanation.

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Chemical Bonding questions and exercises with answers

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Worked practice questions

Hydrogen bonding requires hydrogen bonded to a highly electronegative atom that also:

  1. carries at least one lone pair of electrons
  2. holds a full positive formal charge
  3. belongs to the third period or lower
  4. forms at least two double bonds
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Correct answer: A. carries at least one lone pair of electrons

1. Two conditions must both hold for a hydrogen bond to form. 2. First, hydrogen must be covalently bonded to a small, highly electronegative atom — nitrogen, oxygen or fluorine. 3. Second, that electronegative atom must carry at least one lone pair, which is what the neighbouring hydrogen is attracted to. 4. Water qualifies because oxygen has two lone pairs; ammonia qualifies because nitrogen has one. 5. Missing the lone-pair condition is why candidates could not explain which molecules hydrogen bond and which do not. _Source: NECTA ACSEE 2023 Chemistry 132/1, Question 3: Chemical Bonding_

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o-nitrophenol and p-nitrophenol differ in that they show, respectively:

  1. intermolecular and intramolecular bonding
  2. ionic and covalent bonding throughout
  3. intramolecular and intermolecular bonding
  4. covalent and metallic bonding throughout
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Correct answer: C. intramolecular and intermolecular bonding

1. In o-nitrophenol the nitro group sits next to the hydroxyl group on the ring. 2. They are close enough to bond to each other within the same molecule, which is intramolecular hydrogen bonding. 3. In p-nitrophenol the two groups sit opposite each other, too far apart to reach within one molecule. 4. So p-nitrophenol bonds instead to neighbouring molecules, which is intermolecular hydrogen bonding. 5. Writing 'intrahydrogen' and 'interhydrogen' instead of intramolecular and intermolecular was a recorded wording error. _Source: NECTA ACSEE 2023 Chemistry 132/1, Question 3: Chemical Bonding_

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p-nitrophenol melts at a higher temperature than o-nitrophenol because it:

  1. forms one bond inside each molecule
  2. forms many bonds between molecules
  3. has a much larger molecular mass
  4. contains an extra nitrogen atom
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Correct answer: B. forms many bonds between molecules

1. Melting requires energy to pull separate molecules apart from one another. 2. p-nitrophenol forms many intermolecular hydrogen bonds, linking molecule to molecule. 3. Breaking that network needs a large amount of energy, so the melting point is high. 4. o-nitrophenol's single hydrogen bond is intramolecular, holding one molecule's own groups together. 5. That bond does nothing to hold neighbouring molecules together, so less energy separates them. The two compounds are isomers, so mass is identical. _Source: NECTA ACSEE 2023 Chemistry 132/1, Question 3: Chemical Bonding_

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