Self-test questions: Chapter 12

Self-test questions: Chapter 12

Quiz Content

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For a molecule containing one nitrogen atom, its molecular ion will have an odd mass number.

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Chlorine produces a molecular isotope ratio of 50:50

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Which of the following bonds will give the strongest IR absorption.

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It is possible to distinguish between enantiomers by 1H-NMR.

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How many proton signals would 1-phenylethan-1-one have in its 1H NMR spectrum.

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By 1H NMR spectroscopy, the expected signal intensity for the three lines of an triplet is 1:1:1.

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Each degree of unsaturation confirms the presence of either a pi-bond or a ring structure.  Based on this, select which of the following are true. Please select all that apply.

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