Photo AI

Isomers X and Y have the molecular formula C3H8O Isomer X Isomer Y 07.1 Give the IUPAC name for isomer X - AQA - A-Level Chemistry - Question 7 - 2019 - Paper 2

Question icon

Question 7

Isomers-X-and-Y-have-the-molecular-formula-C3H8O--Isomer-X-Isomer-Y--07.1-Give-the-IUPAC-name-for-isomer-X-AQA-A-Level Chemistry-Question 7-2019-Paper 2.png

Isomers X and Y have the molecular formula C3H8O Isomer X Isomer Y 07.1 Give the IUPAC name for isomer X. [1 mark] 07.2 Explain how and why isomers X and Y can b... show full transcript

Worked Solution & Example Answer:Isomers X and Y have the molecular formula C3H8O Isomer X Isomer Y 07.1 Give the IUPAC name for isomer X - AQA - A-Level Chemistry - Question 7 - 2019 - Paper 2

Step 1

07.1 Give the IUPAC name for isomer X.

96%

114 rated

Answer

The IUPAC name for isomer X is cyclopropanol.

Step 2

07.2 Explain how and why isomers X and Y can be distinguished by comparing each of their boiling points.

99%

104 rated

Answer

The boiling point of isomer X (cyclopropanol) is generally lower than that of isomer Y due to the presence of hydrogen bonds in isomer Y (which is typically more linear or branched). This allows isomer Y to have stronger intermolecular forces, resulting in a higher boiling point.

Step 3

07.2 Explain how and why isomers X and Y can be distinguished by comparing each of their 13C NMR spectra.

96%

101 rated

Answer

In the 13C NMR spectrum, isomer X will generally show fewer peaks compared to isomer Y due to its symmetrical structure. Isomer X may show 2 peaks corresponding to its unique carbon environments, while isomer Y may have a more complex spectrum, showing multiple peaks in the region of 50-80 ppm, indicating different carbon environments.

Step 4

07.2 Explain how and why isomers X and Y can be distinguished by comparing each of their infrared spectra.

98%

120 rated

Answer

In the infrared spectra, isomer Y is expected to exhibit a characteristic broad O-H stretching vibration around 3200-3600 cm⁻¹ due to the hydroxyl group, while isomer X may show weaker or less defined peaks since it does not contain an alcohol functional group. Furthermore, the fingerprint region of the spectra will be different, allowing for distinct identification of the two isomers.

Join the A-Level students using SimpleStudy...

97% of Students

Report Improved Results

98% of Students

Recommend to friends

100,000+

Students Supported

1 Million+

Questions answered

;