Date | May 2012 | Marks available | 3 | Reference code | 12M.3.sl.TZ2.A3 |
Level | SL | Paper | 3 | Time zone | TZ2 |
Command term | Deduce and Explain | Question number | A3 | Adapted from | N/A |
Question
Deduce the number of peaks in the \(^{\text{1}}{\text{H}}\,{\text{NMR}}\) spectra of 1-bromobutane and 2-bromobutane. Explain how the integration trace can be used to distinguish between the two compounds.
Compare the \(^{\text{1}}{\text{H}}\,{\text{NMR}}\) spectrum of 1-bromo-2-methylpropane with the two spectra considered in (a). Include the number of peaks and the integration trace.
Markscheme
both 1-bromobutane and 2-bromobutane have four peaks;
(ratio of areas in) 1-bromobutane: 3:2:2:2;
(ratio of areas in) 2-bromobutane: 3:1:2:3;
For second and third points accept correct ratios given in a different order.
Accept correct number of hydrogen atoms for each peak instead of area.
three peaks (not four);
ratio of areas/integration trace: 6:1:2;
Accept correct ratio given in a different order.
Examiners report
This is a topic that showed better understanding, but many candidates lost marks as their answers did not focus on integration traces. Thus, it looks like quite a few candidates are actually proficient in this technique, but failed to interpret the question properly. Very few candidates could explain the role of \(^{\text{1}}{\text{H}}\,{\text{NMR}}\) in magnetic resonance imaging. Explanations were very shallow evidencing no clear understanding of this technique.
This is a topic that showed better understanding, but many candidates lost marks as their answers did not focus on integration traces. Thus, it looks like quite a few candidates are actually proficient in this technique, but failed to interpret the question properly. Very few candidates could explain the role of \(^{\text{1}}{\text{H}}\,{\text{NMR}}\) in magnetic resonance imaging. Explanations were very shallow evidencing no clear understanding of this technique.