Acid catalyzed hydrolysis of HOCH2CH2C (CH3) 2CN forms compound A (C6H10O2). A shows a strong peak in its IR spectrum at 1770 cm-1 and the following signals in its 1 H NMR spectrum: 1.27 (singlet, 6 H), 2.12 (triplet, 2 H), and 4.26 (triplet, 2 H) ppm. Draw the structure for A and select the correct answers to complete a mechanism that accounts for its formation.

Question

Dangelo Bartlett

Chemistry

19 September, 08:03

Acid catalyzed hydrolysis of HOCH2CH2C (CH3) 2CN forms compound A (C6H10O2). A shows a strong peak in its IR spectrum at 1770 cm-1 and the following signals in its 1 H NMR spectrum: 1.27 (singlet, 6 H), 2.12 (triplet, 2 H), and 4.26 (triplet, 2 H) ppm. Draw the structure for A and select the correct answers to complete a mechanism that accounts for its formation.

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Answers (2)

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Roger · Answer 1

From the given problem statement we need to hydrolyses HOCH2CH2C (CH3) 2CN structure that forms (C6H10O2)

Peak of IR spectrum=1770 cm^-1

This structure for A involves 6 carbon atoms, four hydrogen atoms and 6 oxygen atoms for a complete reaction to occur.

Jazmin · Answer 2

3,3-dimethyldihydrofuran-2 (3H) - one

Explanation:

The simulated spectrum of molecule = > Figure 1

Mechanism=>Figure2