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Question 21N.2.hl.TZ0.1

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Date November 2021 Marks available [Maximum mark: 10] Reference code 21N.2.hl.TZ0.1
Level hl Paper 2 Time zone TZ0
Command term Determine, Explain, Identify, Predict Question number 1 Adapted from N/A
1.
[Maximum mark: 10]
21N.2.hl.TZ0.1

A 4.406 g sample of a compound containing only C, H and O was burnt in excess oxygen. 8.802 g of CO2 and 3.604 g of H2O were produced.

(a)

Determine the empirical formula of the compound using section 6 of the data booklet.

[3]

Markscheme

«8.802 g44.01 g mol-1=» 0.2000 «mol of C/CO2»

AND «3.604 g18.02 g mol-1=» 0.2000 «mol of H2O»/0.4000 «mol of H»

OR

 «8.802 g44.01 g mol-1×12.01 g mol-1» 2.402 «g of C»

OR

«3.604 g18.02 g mol-1×2×1.01 g mol-1=» 0.404 «g of H» ✔

 

«4.406 g − 2.806 g» = 1.600 «g of O» ✔


«2.402 g12.01 g mol-1=0.2000 mol C; 0.404 g1.01 g mol-1=0.400 mol H; 1.600 g16.00 g mol-1=0.1000 mol O»

C2H4O ✔

 

Award [3] for correct final answer.

(b)

Determine the molecular formula of this compound if its molar mass is 88.12 g mol−1. If you did not obtain an answer in (a) use CS, but this is not the correct answer.

[1]

Markscheme

«88.12 g mol-144.06 g mol-1=2» C4H8O2


C2S2 if CS used.

The following spectrums show the Infrared spectra of propan-1-ol, propanal and propanoic acid.

NIST Mass Spectrometry Data Center Collection © 2021 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. Available at: https://webbook.nist.gov/cgi/cbook.cgi?ID=C71238&Units=SI&Type=IRSPEC&Index=3#IR-SPEC [Accessed 6 May 2020]. Source adapted.

NIST Mass Spectrometry Data Center Collection © 2021 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. Available at: https://webbook.nist.gov/cgi/cbook.cgi?ID=C79094&Units=SI&Mask=80#IR-Spec [Accessed 6 May 2020]. Source adapted.

NIST Mass Spectrometry Data Center Collection © 2021 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. Available at: https://webbook.nist.gov/cgi/cbook.cgi?Name=propanal&Units=SI&cIR=on&cTZ=on#IRSpec [Accessed 6 May 2020]. Source adapted.

(c)

Identify each compound from the spectra given, use absorptions from the range of 1700 cm−1 to 3500 cm−1. Explain the reason for your choice, referring to section 26 of the data booklet.

[3]

Markscheme


Award [1 max] for correctly identifying all 3 compounds without valid reasons given.

Accept specific values of wavenumbers within each range.

(d)

Predict the number of 1H NMR signals, and splitting pattern of the –CH3 seen for propanone (CH3COCH3) and propanal (CH3CH2CHO).

[2]

Markscheme

(e)

Predict the fragment that is responsible for a m/z of 31 in the mass spectrum of propan‑1‑ol. Use section 28 of the data booklet.

[1]

Markscheme

CH3O


Accept any structure i.e. “CH2OH+”.