A compound containing one functional group has IR absorption bands at 3300cm-1 (strong, sharp) and 2150 cm-1.Which substance best matches this information?A) hexan-2-oneB) hexan-3-olC) hex-1-eneD) hexaneE) hex-1-yne

A compound having 1 functional group have 2 IR adsorption band one is at 3300cm-1 which is sharp and…

Answered: cm" (strong, sharp) and 2150 cm. Which…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy

Section12.8: Infrared Spectra Of Some Common Functional Groups

Problem 9P

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Propose a structure consistent with each set of data. C10H14: IR absorptions at 3150–2850, 1600, and 1500 cm−1
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Draw a structure consistent with the following set of data: a hydrocarbon with a molecular ion at m/z = 68 and IR absorptions at 3310, 3000−2850, and 2120cm−1.
Propose a structure consistent with each set of data.a.) C9H10O2: IR absorption at 1718 cm−1 b.) C9H12: IR absorption at 2850–3150 cm−1
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Compounds B and C are isomers with molecular formula C5H9BrO2. The 1H NMR spectrum of compounds B and C are shown below. The IR spectrum corresponding to compound B showed strong absorption bands at 1739, 1225, and 1158 cm-1, while the spectrum corresponding to compound C have strong bands at 1735, 1237, and 1182 cm-1. 1.Based on the information provided, determine the structure of compounds B and C. 2.Assign all peaks in 1H NMR spectrum of compounds B and C.
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cm" (strong, sharp) and 2150 cm. Which substance best matches this information? A) hexan-2-one B) hexan-3-ol C) hex-1-ene D) hexane E) hex-1-yne