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NCEA Level 3 Chemistry (90699) 2005 — page 1 of 2

© New Zealand Qualifications Authority, 2005

All rights reserved. No part of this publication may be reproduced by any means without prior permission of the New Zealand Qualifications Authority.

Assessment Schedule – 2005

Chemistry: Describe and use thermochemical principles (90699) Evidence Statement

Q Evidence Achievement Achievement with

Merit

Achievement with Excellence 1(a) ΔrH = –111 kJ mol–1 (or kJ) Correct answer. No units

required 1(b)

(i) ΔrH = Σ Ebonds brokenΣ Ebonds made

–41.2 = ECO + (2 × 463) – (2 × 743) – 436 ECO = –41.2 – 926 + 436 + 1486

= 954.8 or 955 kJ mol1

Accept answer with 3 significant figures.

OR a valid process which uses bond energies to obtain correct answer

Eg ΔrH = Σ Ebonds broken ( positive values )

+ Σ Ebonds formed ( negative values )

Correct process for calculation. / evidence of correct usage of three ratios in calculation.

eg

2 × 463 – 743 × 2 – 436

Correct mathematical calculation with one math error.

Answer calculated correctly with correct unit.

1(b) (ii)

Relates enthalpy change to bond breaking. Bond breaking : absorbs energy / endothermic.

1(b) (iii)

The double bond is stronger than the single bond as it involves the sharing of two electron pairs rather than one as occurs in the single C–O bond.

More (less) energy : required to break : double (single) bonds.

Explanation links higher bond enthalpy to nature of bond and energy required to break bonds.

one electron pair : C-O OR

two electron pairs : C=O 2(a) Ba(s) + N2(g) + 3O2(g) → Ba(NO3)2(s) Correct equation,

including states.

2(b) Δr= ΣΔfHproducts – ΣΔfHreactants

= (5 × –1676 + 3 × –554) – 3 × (–992)

= –7066 kJ mol–1 or –7070 kJ mol-1 Accept answer with 3 or 4 significant figures.

Correct process for calculation / evidence of correct usage of three ratios in calculation.

eg (5 × –1676 + 3 × –554) – 3 × (–992)

Answer calculated correctly : kJ / kJ mol–1

2(c) (i)

2(c) (ii)

n(jelly-baby) = 4.56 g / 342 g mol–1 = 0.0133 mol

E released = 0.0133 × 2192 kJ = 29.2 kJ OR ΔrH = –29.2 kJ

n(SrCl2) vaporised = 29.2 kJ / 343 kJ mol–1 = 0.0851 mol

m(SrCl2) = 0.0851 mol × 159 g mol–1 = 13.5 g Allow follow-on if answer used from (i) is not 29.2 kJ.

Accept

0.0132 mol jelly-baby 28.8 kJ 0.0841 mol SrCl2 13.4 g SrCl2

Moles and energy (for the moles stated) calculated correctly.

Sign can be positive or negative.

Three correct steps with one error eg input error, calculation error or transcription error.

Four correct steps with correct answers, correct sign and units.

3(a) Hydrogen bonds involve the attraction between the H bonded to an O, N or F atom in one molecule and the non-bonding electrons on O, N or F in another

molecule. Diagram may be included, but must indicate the Hydrogen bond with correct indication of polarity.

H is bonded: highly electronegative element:

Intermolecular force.

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NCEA Level 3 Chemistry (90699) 2005 — page 2 of 2

Q Evidence Achievement Achievement with

Merit

Achievement with Excellence 3(b) • Propanoic acid has lower melting point

than butanoic acid because same intermolecular forces (both acids) but Propanoic acid has a smaller mass / less electrons than butanoic acid hence temporary dipoles are weaker.

• Ethyl ethanoate has a lower melting point because it cannot form hydrogen bonds between molecules, so

intermolecular forces are weaker than for the two acids.

Differences in melting point linked to differences in nature / strength of intermolecular forces.

Temporary dipoles / hydrogen bonding / intermolecular forces:

any two appropriate molecules

Eg butanoic acid has a higher melting point as it has stronger

intermolecular forces than ethyl ethanoate.

Discussion of intermolecular forces and relationship to melting point, mostly correct.

Temporary dipoles c/f H bonding : melting point

AND

butanoic/propanoic acid : ethyl ethanoate discussed OR

butanoic:propanoic acid discussed.

Comprehensive discussion of different inter-molecular forces correctly linked to the variation in melting point for all 3 substances

Temporary dipoles c/f H bonding: melting point

AND

butanoic : propanoic acid : ethyl ethanoate discussed.

Judgement Statement

Achie vement Achie vement with Merit Achie vement with Excellence

FIVE opportunities answered at Achievement level or higher.

5 × A

SIX opportunities answered with at least three at Merit level or higher.

3 × M plus 3 × A

SEVEN opportunities answered with at least TWO at Excellence level and TWO at Merit level.

2 × E plus 2 × M plus 3 × A

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