I just finished Section A for the CSE 2010 May exam in 20 minutes, which I am pretty proud of as it was the 4th exam I've done 
But I've a few questions that I did not understand :/
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Q2)
9.30g of element M formed an oxide with an empirical formula of MO3 and a mass of 17.88g. In what section of the periodic table does this element belong to?
A. Transition Metals <--- Correct answer
B. Alkali Metals
C. Alkaline earths
D. Halogens
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Q6) Consider the 2 molecules below
Molecule I : CH3CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3
Molecule II : CH3CH2CH2CH2CH2CH2CH2CH2COOH
When seperating components using high performance liquid chromatography (HPLC) with a polar stationary phase, molecule I has the
A. longer retention time because it has a higher molar mass.
B. the shorter retention time because it has a higher molar mass.
C. longer retention time because it is non-polar
D. shorter retention time because it is non-polar <-- Correct Answer
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Q8) The peak at 45 of propan-2-ol is most likely to be (Note: Peak at 45 is the base peak, so does that mean the strongest bond?)
A. CH3CHOH
B. CH3CH2O+
C. CH3CHOH+ <--- Correct answer
D. CH2CH2OH+
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Those are basically all the questions I got wrong.. The answers didn't really help as they just stated what the answer was without any explanation :/
Sorry, I could be wrong in saying this, but:
Q2) Since its

, can't we simply conclude that the oxidation state of M is +6. I realise oxidation states do not imply the valency of an ion, but in this case, it does seem like a basic ionic bond. An oxidation no. of +6, means it would have to be a transition metal.
3)Molecule I: Non-Polar
Molecule II: Polar
Stationary Phase: Polar
Hence, Mobile Phase: Non-polar
- While molecular mass does make a difference if the two objects differ greatly, or if they are both polar or both non-polar, its affect is completely masked by intermolecular forces in this case. Hence, Molecule II would have a longer retention time, due to stronger attraction (adsorption) to the stationary phase.
- Therefore, Molecule I, as asked by the question, would have a shorter retention time, due to weaker attraction to the stationary phase, and stronger attraction to the mobile phase, as it is non-polar.

Propan-2-ol has a molar mass of approximately 60. Hence, for a base peak of 45, a

group must have been taken off. Hence, the compound must be

.
- I don't think D would be a correct answer. Since its propan-2-ol and a CH3 group was taken off, the Carbon with the -OH group must have only 3 bonds. In this case, it has all 4 bonds and the adjacent carbon has only 3. This would occur in Propan-1-ol, but not Propan-2-ol.
(Draw a diagram of propan-2-ol - it will make my explanation a lot clearer... I hope)