A compound, C4H₂CIO, has an IR spectrum showing a peak at 1810 cm³1. Its ¹H NMR spectrum has peaks at delta 1.0 (3 H, triplet), 1.7 (2 H, multiplet), and 2.8 (2 H, triplet). Draw its structure in the window below. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. + T [... ۵۰ [] ?

A compound, C4H₂CIO, has an IR spectrum showing a peak at 1810 cm³1. Its ¹H NMR spectrum has peaks at delta 1.0 (3 H, triplet), 1.7 (2 H, multiplet), and 2.8 (2 H, triplet). Draw its structure in the window below. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. + T [... ۵۰ [] ?

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 57AP: Draw structures of compounds that fit the following descriptions: a) An , unsaturated ketone, C9H8O...

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