I got this from the IBO online curriculum centre. It was prepared by another IB Chemistry teacher.
I am not sure if these corrections are all correct. I have also added a couple of my own (italics)
Errata in Neuss, G (2007) Chemistry for the IB Diploma OUP
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Page
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Details
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3
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‘Solutions’ box: ‘amount’ cannot be expressed as g
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4
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Q14a ‘anhydride’ not ‘acid’
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9
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Successive ionisation energies good evidence for shells, first ionisation energies of successive elements good evidence for orbitals.
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24
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s and p bonds (diagram) should interpenetrate
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22
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C60 is not the only fullerene
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31
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Under DHEA: Atoms ‘want’…
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33-34
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DHo should be in kJ mol-1 not just kJ? See Q4 in particular.
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40
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Q16B 2 H2O2 à surely?
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43
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Half-way down: Should be [acid] not [ester]
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43
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Quadratic equations are not required! (See Syllabus 17.2.1 and 18.1.5)
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45
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Ka of H2O is 1.82 x 10-16 pKa=15.7 (= -log[H+][OH-]/[H2O])
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52
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typos in weak acid –strong base titration. [CH3COO-] = 0.5 and substitution into equation of that and [CH3COOH] is also incorrect.
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53
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Q14 – no units given for Ka
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55
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Picky, but: An element can combine without changing oxidation state: nickel carbonyl formation, for example.
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56
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Oxidation potentials given but reduction potentials are conventional (see e.g. table 14 of IB Data Booklet)
Half-cells are not only made by putting a metal in contact with an aqueous solution of its own ions. What about the hydrogen electrode? Iron(ii)/iron (iii) couples?
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62
166
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Amine nomenclature: aminoethane (etc) used but ethylamine (etc) is used on p21 of the IB Data Booklet and p162 of Neuss itself
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96
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Not all fats & oils are triglycerides. Cholesterol and phospholipids for example.
Fats are also used as hormones, electrical insulation in nerves.
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156
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Redundant 2 in 2-methyl-but-2-ene
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162
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‘Trimethylethanoic’? Dimethylpropanoic!
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165
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CHCl3 given for CH3Cl
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166
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Chlorobenzene is less reactive than benzene, not more reactive as stated.
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169
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Use ‘EE’ function rather than x10^ keys…
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176
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Under acids and bases #5 is A
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