This question is about compound X with the empirical formula C2H6O - AQA - A-Level Chemistry - Question 6 - 2022 - Paper 2
Question 6
This question is about compound X with the empirical formula C2H6O.
Figure 2 shows the infrared spectrum of X.
Figure 3 shows the 1H NMR spectrum of X.
Table 3 gi... show full transcript
Worked Solution & Example Answer:This question is about compound X with the empirical formula C2H6O - AQA - A-Level Chemistry - Question 6 - 2022 - Paper 2
Step 1
Chemical shift δ / ppm: 3.9
96%
114 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The peak at 3.9 ppm in the 1H NMR spectrum indicates the presence of a hydrogen atom attached to a carbon atom that is adjacent to an electronegative atom, likely oxygen. This suggests the presence of an -O-CH2- group, consistent with the empirical formula.
Step 2
Chemical shift δ / ppm: 3.7
99%
104 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The peak at 3.7 ppm corresponds to a hydrogen atom in a different environment, potentially an -O-CH3 group. This further supports the presence of an alcohol or ether functional group.
Step 3
Chemical shift δ / ppm: 2.1
96%
101 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The peak at 2.1 ppm is indicative of hydrogen atoms in a more deshielded environment, possibly associated with a methylene (CH2) group. This suggests that we may have the -CH2- connected to another carbon atom or functional group.
Step 4
Chemical shift δ / ppm: 1.2
98%
120 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The doublet observed at 1.2 ppm implies the presence of terminal methyl groups (CH3) in the molecular structure, reinforcing the presence of a straight-chain or branched hydrocarbon.
Step 5
Deduction of Structure
97%
117 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
Based on the data from the NMR and IR spectra, as well as the peak integration values from Table 3, we can deduce that the structure of compound X is likely to be ethanol (C2H5OH) or a related compound containing similar functional groups, such as an ether or other alcohols. The characteristic peaks and integrations correlate well with a molecular structure suggesting C2H6O.