Zadanie 18
Which compound could produce this mass spectrum? A. Butanone B. Butanal C. Butan-1-ol D. Butan-2-ol
- Tabela do uzupełnienia
- Materiał graficzny
Deduce structural features of an organic compound from its mass spectrum: the molecular ion peak gives the molar mass and fragment peaks (for example loss of 15 for CH3 or 17 for OH) identify groups, using the fragment table in the data booklet.
Tę umiejętność sprawdza 17 zadań wzorowanych na arkuszach IB z lat 2022–2026.
Which compound could produce this mass spectrum? A. Butanone B. Butanal C. Butan-1-ol D. Butan-2-ol
The mass spectrum of carbonyl dibromide is shown below. Bromine has two isotopes, and , of almost equal abundance. (i) Explain the origin of the peaks that appear at m/z values smaller than those of the molecular ion. (ii) Deduce…
In the mass spectrum of Y, the molecular ion peak appears at m/z 88. (i) Y contains no multiple carbon–carbon bonds and no rings. Deduce its molecular formula. Use section 7 of the data booklet. Shown below is the high-resolution NMR spectrum of Y,…
The mass spectra of four compounds are shown below. Which is the spectrum of propanal, CH3CH2CHO? Use section 22 of the data booklet. A. spectrum A B. spectrum B C. spectrum C D. spectrum D
What is the molecular formula of the compound with empirical formula CH2 and the following mass spectrum? A. C4H8 B. C6H12 C. C7H14 D. C8H16
Propenal can be oxidised to compound G. G produces bubbles of gas when it is added to aqueous sodium hydrogencarbonate. The mass spectrum of G is shown. Deduce what G is and give two reasons, based on the mass spectrum.
A student converts methyl 4-hydroxybenzoate (Mr = 152.15) into methyl 4-methoxybenzoate (Mr = 166.18) by replacing the hydrogen atom of the phenol group with a methyl group. The product was analysed in a mass spectrometer. Suggest how…
The mass spectrum of 3-methylbutanoic acid is shown. (i) Suggest why the spectrum shows a small peak at m/z 103. (ii) Identify the fragments responsible for the peaks at m/z 87 and m/z 57. Use section 22 of the data booklet.
Which statements about the molecular ion, M+, in a mass spectrum are correct? I. The M+ peak is always the peak of greatest intensity in the spectrum. II. The M+ ion forms when a molecule loses one electron. III. The m/z…
An unknown organic compound, X, contains only carbon, hydrogen and oxygen. Elemental analysis shows that it contains 54.5 % carbon and 36.3 % oxygen by mass. (i) Determine the empirical formula of X. The mass spectrum of X is shown. (ii) Identify the species…
A forensic laboratory identifies a solvent by mass spectrometry. The mass spectrum of a sample of pentan-3-one, CH3CH2COCH2CH3, Mr 86, is shown. Explain how the peaks at m/z 86 and m/z 57 support the identification of the compound as…
Propan-1-ol can be identified by a variety of analytical techniques. Predict the structures of three possible fragments you would expect from the mass spectrum of propan-1-ol. Use section 22 of the data booklet.
The mass spectrum of ibuprofen (Mr = 206) has a peak at m/z = 161. Suggest which fragment, lost from the molecular ion, could account for this peak. Use section 22 of the data booklet.
Salbutamol, used to treat asthma, has a relative molecular mass Mr = 239. Its mass spectrum has a peak at m/z = 221. Suggest a neutral fragment whose loss could account for this peak. Use section 22 of the data booklet.
(i) State two features that show that ethene and propene are members of the same homologous series. (ii) The mass spectrum of pentane is shown. Suggest the species responsible for peak R. Use section 22 of the data booklet.
Which compound produces this mass spectrum? A. Propanoic acid, CH3CH2COOH B. Ethyl methanoate, HCOOCH2CH3 C. Butan-1-ol, CH3CH2CH2CH2OH D. Methyl ethanoate, CH3COOCH3
What information about pentan-2-one, CH3COCH2CH2CH3, can be obtained from mass spectrometry (MS), infrared (IR) spectroscopy and 1H NMR spectroscopy? A. MS: the compound contains a carbonyl group; IR: the molar mass is 86 g mol−1;…
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